6655 NP_001070868 S119F not found in SNVbox database
7060 NP_109597 S132C not found in SNVbox database
7172 NP_705833 S258F not found in SNVbox database
7269 NP_705833 D632N not found in SNVbox database
951 NP_705833 D214H not found in SNVbox database
1865 NP_001070868 T538M not found in SNVbox database
2488 NP_705833 G213A not found in SNVbox database
4027 NP_001070868 E184Q not found in SNVbox database
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr19:58862856 G>A maps to NM_130786.3 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:58864523 G>C maps to NM_130786.3 S37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr19:58863874 G>A maps to NM_130786.3 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr10:52569777 C>T maps to NM_138932.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr10:52570845 A>G maps to NM_138932.2 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr16:7568219 G>A maps to NM_145891.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr16:7703922 C>A maps to NM_145891.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr16:7645612 C>T maps to NM_145891.2 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr16:7568297 C>T maps to NM_145891.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr16:7760720 G>T maps to NM_145891.2 G411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr16:7759105 A>C maps to NM_145891.2 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr12:9251329 G>C maps to NM_000014.4 S575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr12:9243949 C>T maps to NM_000014.4 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:9259152 G>A maps to NM_000014.4 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:9262487 C>T maps to NM_000014.4 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr12:9232331 G>C maps to NM_000014.4 V978V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr12:9225251 G>C maps to NM_000014.4 L1324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr12:9229989 G>A maps to NM_000014.4 L1101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr12:9232355 A>C maps to NM_000014.4 Y970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr12:9266108 G>C maps to NM_000014.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr12:9006742 T>A maps to NM_144670.3 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr12:9020632 C>T maps to NM_144670.3 Q1305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr12:8988245 C>T maps to NM_144670.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr12:8975880 C>T maps to NM_144670.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr12:9009904 C>T maps to NM_144670.3 I998I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr12:9009895 G>A maps to NM_144670.3 T995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:8995750 T>C maps to NM_144670.3 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr12:9001416 C>T maps to NM_144670.3 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:43089309 G>A maps to NM_017436.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr22:43089096 G>A maps to NM_017436.4 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:137843159 C>T maps to NM_016161.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr3:137849772 G>C maps to NM_016161.2 S109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr3:137849805 G>C maps to NM_016161.2 S98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr3:137843183 G>A maps to NM_016161.2 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr12:53703044 C>T maps to NM_015665.5 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr12:125558470 C>T maps to NM_023928.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr12:125591756 C>T maps to NM_023928.3 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr3:151545956 A>G maps to NM_001086.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr3:151545701 C>T maps to NM_001086.2 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:151451904 G>T maps to NM_207365.3 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr1:12704654 C>A maps to NM_001013630.1 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:12726458 C>T maps to NM_001013630.1 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr4:170988518 T>C maps to ENST00000509167 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:170983084 C>T maps to ENST00000509167 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr2:69759276 C>T maps to NM_014911.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr2:69732794 G>A maps to NM_014911.3 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr2:69706134 A>T maps to NM_014911.3 T876T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:219131677 G>A maps to ENST00000444053 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:70301625 G>A maps to ENST00000418685 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:70292972 G>C maps to ENST00000418685 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr16:70301634 G>C maps to ENST00000418685 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:70303573 C>T maps to ENST00000418685 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr16:70301613 A>G maps to ENST00000418685 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr6:44279134 C>T maps to NM_020745.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr6:44273473 C>T maps to NM_020745.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr6:44278752 G>A maps to NM_020745.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr6:44280985 G>C maps to NM_020745.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:41116251 G>A maps to NM_001136042.2 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr17:41108501 C>T maps to NM_001136042.2 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr4:57250455 G>A maps to NM_181806.2 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr4:57221466 G>A maps to NM_181806.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr11:105950306 G>A maps to NM_015423.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr11:105962116 A>C maps to NM_015423.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr7:121738841 T>C maps to NM_005763.3 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr7:121731847 G>C maps to NM_005763.3 S642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr7:121733142 A>C maps to NM_005763.3 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr17:35343959 C>T maps to NM_012138.3 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:35348107 G>A maps to NM_012138.3 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr17:35376309 C>T maps to NM_012138.3 R469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr17:79095146 C>T maps to NM_001080395.2 T863T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr17:79094709 G>C maps to NM_001080395.2 S1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr17:79094975 G>A maps to NM_001080395.2 F920F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr9:107576708 T>C maps to NM_005502.3 S1262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr9:107580988 G>A maps to NM_005502.3 L1139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr9:107599777 C>G maps to NM_005502.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr9:107646763 G>A maps to NM_005502.3 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr17:67178945 G>C maps to NM_080282.3 S834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:67149525 C>A maps to NM_080282.3 L1352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:67170478 T>C maps to NM_080282.3 S1035S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr17:67197702 C>T maps to NM_080282.3 E371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr17:67161149 G>A maps to NM_080282.3 F1079F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr2:215919340 G>C maps to NM_173076.2 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr2:215976353 A>C maps to NM_173076.2 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr2:215854126 C>T maps to NM_173076.2 W1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:215851336 G>C maps to NM_173076.2 L1364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr2:215884507 G>A maps to NM_173076.2 R434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:215815800 G>A maps to NM_173076.2 F2218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr2:215854151 G>A maps to NM_173076.2 Q1244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:215852368 A>C did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:215855515 G>A maps to NM_173076.2 I1178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr2:215821415 G>A maps to NM_173076.2 G2068G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr2:215809795 C>T maps to NM_173076.2 S2424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr7:48318506 A>G maps to NM_152701.3 E2572E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr7:48311667 G>A maps to NM_152701.3 W802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr7:48280472 C>T maps to NM_152701.3 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr7:48284187 G>A maps to NM_152701.3 W426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:48311968 C>G maps to NM_152701.3 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:48273723 G>A maps to NM_152701.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:48311732 G>T maps to NM_152701.3 E824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr7:48559671 C>G maps to NM_152701.3 V4611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr7:48556397 C>A maps to NM_152701.3 S4573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr7:48312040 A>G maps to NM_152701.3 A926A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr7:48654967 A>G maps to NM_152701.3 K4944K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr7:48349570 C>T maps to NM_152701.3 L3117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr7:48318167 T>C maps to NM_152701.3 F2459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr7:48312657 C>G maps to NM_152701.3 S1132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:48319281 C>T maps to NM_152701.3 L2831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:48318543 G>T maps to NM_152701.3 E2585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr7:48428736 C>T maps to NM_152701.3 V3858V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:48316090 A>G maps to NM_152701.3 L2276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr7:48314854 G>A maps to NM_152701.3 L1864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr7:48312667 C>A maps to NM_152701.3 V1135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr7:48312162 C>G maps to NM_152701.3 S967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:48313614 C>G maps to NM_152701.3 S1451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:48349689 G>C maps to NM_152701.3 L3156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:48335302 G>T maps to NM_152701.3 E2988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr7:48317779 C>G maps to NM_152701.3 S2330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr7:48316033 G>T maps to NM_152701.3 L2257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr7:48314883 C>G maps to NM_152701.3 S1874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:139907258 C>T maps to ENST00000355090 Q1692Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:139906346 G>A maps to ENST00000355090 V1858V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr9:139908490 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:139914853 G>C maps to ENST00000355090 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr9:139909935 G>A maps to ENST00000355090 L1239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr9:139909941 G>T maps to ENST00000355090 L1237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr16:2349534 T>G did not map to a codon.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr16:2326725 G>C maps to NM_001089.2 V1688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:2331114 C>A maps to NM_001089.2 T1424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr16:2328305 G>A maps to NM_001089.2 I1567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr1:94496054 G>A maps to NM_000350.2 F1427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:94476480 C>T maps to NM_000350.2 E1863E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:94496676 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:94471002 G>A maps to NM_000350.2 I2047I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr1:94544952 C>T maps to NM_000350.2 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:94564373 C>A maps to NM_000350.2 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:94473257 T>G maps to NM_000350.2 T1979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:94463666 C>G did not map to a codon.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr1:94574255 G>A maps to NM_000350.2 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:94502335 C>T maps to NM_000350.2 L1274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr1:94528161 C>T maps to NM_000350.2 Q636Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr17:67270111 G>A maps to ENST00000392677 Q918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:67255905 G>C maps to ENST00000392677 L1225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:67250580 C>T maps to ENST00000392677 L1374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr17:67243770 G>A maps to ENST00000392677 L1613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr17:67084353 C>A maps to NM_080284.2 E1218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr17:67125786 G>A maps to NM_080284.2 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr17:67130778 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr17:67132374 C>T maps to NM_080284.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr19:1052103 G>A maps to NM_019112.3 L1042L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr19:1057946 C>A maps to NM_019112.3 S1638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr19:1057958 C>T maps to NM_019112.3 S1642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr19:1058720 C>T maps to NM_019112.3 Q1752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:1055908 G>C maps to NM_019112.3 L1403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr19:1051273 G>A maps to NM_019112.3 V935V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr19:1062219 C>T maps to NM_019112.3 Q1874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr19:1055152 G>A maps to NM_019112.3 W1336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:1065157 G>C maps to NM_019112.3 T2091T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr19:1058680 G>A maps to NM_019112.3 V1738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr19:1053409 G>A maps to NM_019112.3 L1101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr19:1051201 G>C maps to NM_019112.3 L911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr17:66913592 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:66872822 C>T maps to NM_007168.2 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr17:66933152 A>G maps to NM_007168.2 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:66890330 T>A maps to NM_007168.2 R967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:66914236 G>A maps to NM_007168.2 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr17:66873736 C>A maps to NM_007168.2 L1334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr17:66864297 C>T maps to NM_007168.2 Q1558Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr17:66872828 G>C maps to NM_007168.2 L1365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:66925207 G>A maps to NM_007168.2 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:66872841 A>C maps to NM_007168.2 L1361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr17:66899518 G>A maps to NM_007168.2 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr17:66881390 G>A maps to NM_007168.2 F1125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr17:66899530 A>C maps to NM_007168.2 G796G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr17:66972296 G>T maps to NM_080283.3 L1585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr17:66988370 G>A maps to NM_080283.3 R1221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:67023211 G>C maps to NM_080283.3 S652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr17:67023134 C>A maps to NM_080283.3 E678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr17:67023239 C>A maps to NM_080283.3 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:67012525 G>A maps to NM_080283.3 H969H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr17:67008196 G>A maps to NM_080283.3 R1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr17:67023472 G>A maps to NM_080283.3 Q637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr7:87173536 C>A maps to NM_000927.3 E707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr7:87179184 A>G maps to NM_000927.3 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr7:87190667 C>G maps to NM_000927.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr7:87183160 C>A maps to NM_000927.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr7:87160642 C>T maps to NM_000927.3 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:229666155 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr2:169814518 C>G maps to NM_003742.2 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr2:169791707 G>A maps to NM_003742.2 F1014F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:87041263 G>A maps to NM_018849.2 R957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr7:87031441 G>A maps to NM_018849.2 V1277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr7:20795241 C>T maps to NM_001163941.1 Q1257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr7:20691116 A>G maps to NM_001163941.1 Q469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:20685492 G>T maps to NM_001163941.1 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr2:220079683 G>A maps to NM_005689.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr2:220083370 C>A maps to NM_005689.2 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:220077976 G>A maps to NM_005689.2 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr2:220075191 C>T maps to NM_005689.2 T754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr23:74290269 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr23:74291393 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:74289135 T>C did not map to a codon.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr23:74273274 T>A did not map to a codon.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr23:74288843 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:150738288 C>A maps to ENST00000297504 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:150732744 G>A maps to ENST00000297504 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr7:150732783 G>A maps to ENST00000297504 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr7:150730952 C>A maps to ENST00000297504 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr7:150730928 G>A maps to ENST00000297504 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:123424765 C>T maps to NM_203444.2 K545K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:16215926 C>T maps to ENST00000399408 V1172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:16110411 C>T maps to ENST00000399408 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:16184357 C>T maps to ENST00000399408 Q853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr16:16208824 C>T maps to ENST00000399408 F1104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:16208824 C>T maps to ENST00000399408 F1104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:16130385 C>T maps to ENST00000399408 N245N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:16103742 C>G maps to ENST00000399408 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr6:43400683 C>T maps to NM_033450.2 H279H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:43415549 C>T maps to NM_033450.2 I1250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr6:43403843 A>G maps to NM_033450.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:43415672 C>G maps to NM_033450.2 L1291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr16:48201214 G>T maps to NM_032583.3 L1373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:48250114 C>T maps to NM_032583.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr16:48210949 G>A maps to NM_032583.3 I1141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:48237195 G>C maps to NM_032583.3 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr16:48234386 C>A maps to NM_032583.3 G628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:48258267 C>T maps to NM_032583.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr16:48221239 G>A maps to NM_032583.3 P935P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:48177900 C>T maps to NM_033226.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:48177915 G>A maps to NM_033226.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr16:48130785 G>A maps to NM_033226.2 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:48162608 G>A maps to NM_033226.2 Q426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:48174660 G>T maps to NM_033226.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr16:48162639 G>C maps to NM_033226.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr16:48177888 C>T maps to NM_033226.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:48138255 G>A maps to NM_033226.2 F899F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr16:48173142 G>A maps to NM_033226.2 Y254Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr10:101604194 C>T maps to NM_000392.3 I1320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr10:101571350 A>T maps to NM_000392.3 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr10:101590496 G>C maps to NM_000392.3 L924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr10:101591825 C>A maps to NM_000392.3 R1066R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:48745048 C>G maps to NM_003786.3 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:48750879 C>T maps to NM_003786.3 F820F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr17:48755295 C>T maps to NM_003786.3 I1190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr17:48761080 G>C maps to NM_003786.3 L1306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr17:48745849 G>A maps to NM_003786.3 Q614Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:48735441 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr13:95726578 C>T did not map to a codon.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr13:95735499 C>T maps to NM_005845.3 V860V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr13:95861689 C>T maps to NM_005845.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr13:95816711 G>A maps to NM_005845.3 Q699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr13:95815869 G>T maps to NM_005845.3 S736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr3:183670915 G>A maps to NM_005688.2 F875F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr3:183670873 C>T maps to NM_005688.2 G889G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr3:183705700 C>A maps to NM_005688.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr3:183689496 G>A maps to NM_005688.2 Q539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr3:183643380 G>A maps to NM_005688.2 L1392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr3:183695350 G>C maps to NM_005688.2 S453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr3:183695388 G>A maps to NM_005688.2 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr3:183707129 C>T maps to NM_005688.2 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr3:183670894 G>T maps to NM_005688.2 Y882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr3:183683217 G>A maps to NM_005688.2 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr3:183706416 G>C maps to NM_005688.2 S129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr3:183732066 G>A maps to NM_005688.2 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr3:183679423 C>A maps to NM_005688.2 E752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr16:16297361 C>T maps to NM_001171.5 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:16259686 G>T maps to NM_001171.5 I1033I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr16:16297331 G>A maps to NM_001171.5 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:16244625 C>T maps to NM_001171.5 V1404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr16:16263638 G>C maps to NM_001171.5 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr16:16259557 G>A maps to NM_001171.5 V1076V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr11:17427078 G>A maps to ENST00000302539 L1122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:17474773 G>A maps to ENST00000302539 Y356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:17428509 G>T maps to ENST00000302539 I1030I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:17483348 C>T maps to ENST00000302539 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr11:17418788 G>T maps to ENST00000302539 R1314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr11:17483189 G>A maps to ENST00000302539 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr11:17430000 C>A maps to ENST00000302539 E921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr12:22059096 A>G maps to NM_005691.2 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr12:22015989 T>A did not map to a codon.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr12:21997777 A>G maps to NM_005691.2 T1056T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr12:22015984 C>T maps to NM_005691.2 R747R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:21995252 G>A maps to NM_005691.2 A1156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr12:21995342 C>T maps to NM_005691.2 G1126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr12:22061130 C>A maps to NM_005691.2 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr23:152991099 C>T did not map to a codon.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr23:152991100 C>T did not map to a codon.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr23:152994805 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr23:152991183 G>A did not map to a codon.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr23:152991451 C>T did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr23:152991335 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr23:153001575 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr23:153006170 G>A did not map to a codon.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr12:40010951 G>A maps to NM_005164.3 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:39967516 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:94884132 C>A maps to ENST00000454898 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr14:74759321 G>A maps to NM_005050.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr7:150912710 G>A maps to NM_005692.3 Y503Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr3:183910613 C>T maps to NM_018358.2 F560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr3:183904000 G>A maps to NM_018358.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr21:43714662 C>T maps to NM_004915.3 F567F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr21:43704786 C>T maps to NM_004915.3 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:43708134 G>A maps to NM_004915.3 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr21:43621830 C>T maps to NM_207627.1 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr21:43704774 C>T maps to NM_004915.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr4:89016703 G>A maps to NM_004827.2 Q569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr4:89039319 G>C maps to NM_004827.2 S261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr11:119031755 C>T maps to NM_001142505.1 F627F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr11:119031018 C>G maps to NM_001142505.1 S507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:44041637 G>A maps to NM_022436.2 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr2:44051154 G>C maps to NM_022436.2 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr2:44040380 C>T maps to NM_022436.2 E610E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:44041646 G>A maps to NM_022436.2 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr2:44053553 G>A maps to NM_022436.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr2:44101117 C>T maps to NM_022437.2 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:44102358 G>A maps to NM_022437.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr2:44099184 C>G maps to NM_022437.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr2:27351314 C>A maps to NM_032604.3 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr7:73151302 G>A maps to NM_148912.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr20:25284236 G>A maps to NM_015600.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr20:25282957 G>A maps to NM_015600.3 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr20:25295600 C>G maps to NM_015600.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr20:25297682 C>A did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr20:25284236 G>C maps to NM_015600.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr13:108881640 C>T maps to NM_032859.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:27893503 G>A maps to NM_198147.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr18:19239255 C>T maps to NM_138340.4 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr14:23078693 C>T maps to NM_022060.2 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:43760022 G>A maps to NM_016006.4 *350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr3:58242397 C>T maps to NM_020676.5 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr3:58271095 C>G maps to NM_020676.5 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:17405303 G>A maps to NM_024527.4 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:17411696 C>T maps to NM_024527.4 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr2:204231718 G>A maps to ENST00000295851 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr17:47295120 G>A maps to NM_016428.2 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr3:100595362 G>A maps to ENST00000471714 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr3:100471700 A>C maps to ENST00000471714 Y1675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr9:133759599 C>T maps to NM_007313.2 I660I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr9:133759971 G>A maps to NM_007313.2 K784K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:133760865 C>G maps to NM_007313.2 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:133750278 G>A maps to NM_007313.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr9:133750302 G>A maps to NM_007313.2 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:179100500 G>A maps to NM_007314.3 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:179095625 G>A maps to NM_007314.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:179089339 G>A maps to NM_007314.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:116197662 G>T maps to ENST00000277895 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr10:116307491 C>T maps to ENST00000277895 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:116307535 C>G did not map to a codon.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr10:116207741 G>A maps to ENST00000277895 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr4:7985050 G>C maps to NM_001130083.1 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr4:7985014 T>C maps to NM_001130083.1 K600K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:8029549 G>C maps to NM_001130083.1 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:148563060 C>T maps to NM_014945.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr5:148637876 C>T maps to NM_014945.2 F654F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr5:148620284 G>C maps to NM_014945.2 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr7:150554797 C>A maps to ENST00000416793 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr7:150555034 G>T maps to ENST00000416793 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr17:1003884 G>A maps to NM_021962.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr17:1003906 G>A maps to NM_021962.2 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr17:986834 G>C maps to NM_021962.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr17:1028676 G>A maps to NM_021962.2 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr17:953842 G>A maps to NM_021962.2 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr6:26598533 C>T maps to NM_013375.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:127391915 C>T maps to NM_172027.2 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr3:127399293 C>T maps to NM_172027.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:34182491 G>A maps to NM_145804.2 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr18:47311613 C>A maps to NM_006111.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr17:35603882 G>A maps to NM_198834.1 I773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:35512648 G>A maps to NM_198834.1 L1801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr17:35468535 G>A maps to NM_198834.1 F2165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:35627677 G>A maps to NM_198834.1 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr17:35545336 G>A maps to NM_198834.1 I1552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr17:35548096 G>C maps to NM_198834.1 L1512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:35631156 G>C maps to NM_198834.1 S312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr17:35479508 G>A maps to NM_198834.1 R2028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr17:35615270 T>G maps to NM_198834.1 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr17:35454053 C>G maps to NM_198834.1 L2256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr17:35578655 A>T maps to NM_198834.1 S1224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:35580516 G>A maps to NM_198834.1 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr17:35609867 G>A maps to NM_198834.1 Q641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr17:35454832 G>A maps to NM_198834.1 Q2218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr17:35512648 G>A maps to NM_198834.1 L1801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:35634898 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:109577218 G>A maps to NM_001093.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr12:109577566 G>T maps to NM_001093.3 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:109604794 G>A maps to NM_001093.3 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr12:109671618 C>T maps to NM_001093.3 A1402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr12:109670584 C>T maps to NM_001093.3 A1371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:112174761 C>T maps to NM_001136538.1 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr12:112182843 C>T maps to NM_001136538.1 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr12:112171867 G>C maps to NM_001136538.1 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr3:132360901 C>A maps to NM_032169.4 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr3:128629633 C>T maps to NM_014049.4 F581F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr3:128627062 G>A maps to NM_014049.4 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr1:76215150 C>T maps to ENST00000370834 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr12:121176690 G>A maps to NM_000017.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr12:121176980 G>A maps to NM_000017.2 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:121174922 C>T maps to NM_000017.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr10:124793888 G>T maps to NM_001609.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr10:124797329 G>A maps to NM_001609.3 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr10:124813244 G>A maps to NM_001609.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr17:7126020 C>G maps to ENST00000356839 S351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:7127556 G>A maps to ENST00000356839 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr15:89379445 T>A maps to NM_013227.3 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr15:89388874 G>A maps to NM_013227.3 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:89401275 G>A maps to NM_013227.3 T1820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr15:89398557 G>A maps to NM_013227.3 V914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:89417255 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr15:89417121 G>A maps to NM_013227.3 Q2461Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr15:89402346 G>A maps to NM_013227.3 V2177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr15:89403659 C>T maps to NM_013227.3 H2312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr15:89391183 G>A maps to NM_013227.3 K549K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr15:89386724 C>T maps to NM_013227.3 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr15:89402202 G>C maps to NM_013227.3 L2129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr15:89402202 G>C maps to NM_013227.3 L2129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:89414739 C>T maps to NM_013227.3 I2358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr15:89390570 G>A maps to NM_013227.3 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr15:89401752 T>C maps to NM_013227.3 S1979S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:7250444 C>T maps to NM_014716.3 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:7246712 C>T maps to NM_014716.3 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr3:195063205 C>T maps to NM_012287.5 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:195102745 C>A maps to NM_012287.5 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr3:195000074 T>C maps to NM_012287.5 Q773Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr3:195000151 C>A maps to NM_012287.5 E748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr3:195102685 G>A maps to NM_012287.5 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:1234002 C>A maps to NM_030649.2 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr1:1231146 G>A maps to NM_030649.2 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:1235579 G>A maps to NM_030649.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr1:1233312 C>T maps to NM_030649.2 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:1238300 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr11:108009665 T>C maps to NM_000019.3 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr1:226340228 C>T maps to NM_022735.3 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr17:43215294 C>T maps to NM_001135706.1 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr17:43220895 C>A maps to NM_001135706.1 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:43214492 G>A maps to NM_001135706.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr17:43220959 C>T maps to NM_001135706.1 C326C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:43213594 G>A maps to NM_001135706.1 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr17:43214493 A>C maps to NM_001135706.1 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:27512344 C>A maps to ENST00000375888 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr10:27508694 T>C maps to ENST00000375888 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr10:27512268 G>C maps to ENST00000375888 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr10:27493477 T>A maps to ENST00000375888 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr10:27497270 G>A maps to ENST00000375888 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr10:27506990 C>T maps to ENST00000375888 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:180471335 C>T maps to NM_032360.3 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr10:15120549 C>G maps to NM_001039844.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr10:15121000 C>G maps to NM_001039844.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:15121000 C>T maps to NM_001039844.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr10:15120964 G>C maps to NM_001039844.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr17:31351024 C>T maps to NM_183377.1 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:31618695 G>C maps to NM_183377.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr17:32483410 C>T maps to NM_001094.4 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:31415925 C>A maps to NM_183377.1 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr17:31350877 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr7:150749531 C>T maps to NM_020321.2 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:220379724 G>A maps to NM_018674.4 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:220396822 G>A maps to NM_018674.4 Q403Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:156751109 G>C maps to NM_017419.2 Y472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr11:44089203 C>T maps to NM_032592.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr11:44089397 G>A maps to NM_032592.3 W74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:44097104 C>G maps to NM_032592.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:44098827 G>A did not map to a codon.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr11:44105035 G>A maps to NM_032592.3 K439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:44069599 C>G maps to NM_001031854.2 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:67694243 A>G maps to NM_001082486.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:67694192 C>G maps to NM_001082486.1 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr16:67692068 C>T maps to NM_001082486.1 Q428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr16:67694228 G>T maps to NM_001082486.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr16:67693321 G>A maps to NM_001082486.1 C224C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr16:67693693 C>A maps to NM_001082486.1 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr16:67694365 G>A maps to NM_001082486.1 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr17:61562332 G>A maps to NM_152830.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:61560830 C>T maps to NM_000789.3 Q500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:61560532 C>T maps to NM_000789.3 R496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:61571301 G>A maps to NM_000789.3 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr23:15605981 C>A did not map to a codon.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr23:15599439 T>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:15605899 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:15591523 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr23:15588450 C>T did not map to a codon.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr23:15619007 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:15610401 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr23:15610442 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:6333547 G>A maps to NM_133492.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr9:19435038 C>T maps to NM_001010887.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr11:76731358 C>T maps to NM_018367.5 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr7:100490232 C>T maps to NM_000665.3 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr7:100491460 G>A maps to NM_000665.3 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr7:100491562 C>T maps to NM_000665.3 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr7:100490863 G>A maps to NM_000665.3 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr14:23559766 G>A maps to NM_014977.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr14:23530571 G>C maps to NM_014977.3 S1178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:23549688 G>A maps to NM_014977.3 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr14:23548899 C>T maps to NM_014977.3 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr14:23533581 G>A maps to NM_014977.3 I866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr14:23547472 C>T maps to NM_014977.3 G728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:40070072 G>A maps to ENST00000401700 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:40069976 C>T maps to ENST00000401700 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:40068699 C>T maps to ENST00000401700 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr17:40049371 C>T maps to ENST00000401700 Q549Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:40028326 C>T maps to ENST00000401700 G961G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:40039485 C>A did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:40025747 T>A maps to ENST00000401700 V1054V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr17:40070024 G>C maps to ENST00000401700 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:40027971 C>T maps to ENST00000401700 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr17:40042446 C>A maps to ENST00000401700 G708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr17:40042426 G>A maps to ENST00000401700 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr17:40055021 G>A maps to ENST00000401700 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:40040508 G>A maps to ENST00000401700 F741F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:40035105 C>T maps to ENST00000401700 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:135655918 C>T maps to NM_138326.2 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr2:135616889 G>A maps to NM_138326.2 W54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:135602801 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:96747139 G>A maps to NM_020186.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr9:32421005 C>T maps to NM_002197.2 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr9:32431747 G>A maps to NM_002197.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr9:32407325 G>C maps to NM_002197.2 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr22:41914569 C>T maps to ENST00000396512 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr22:41923344 G>C maps to ENST00000396512 S694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr22:41865167 A>G maps to ENST00000396512 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr22:41911841 A>T maps to ENST00000396512 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:55051508 G>A maps to NM_015547.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:55073614 G>A maps to NM_015547.3 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr5:80626218 T>C maps to NM_130767.2 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:80628324 G>A maps to NM_130767.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr5:80640790 G>A maps to NM_130767.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr5:80626731 C>T maps to NM_130767.2 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr6:24701841 G>A maps to NM_018473.3 *141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr1:6393575 C>T maps to NM_007274.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr20:44472958 G>A maps to NM_005469.3 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr20:44472253 G>A maps to NM_005469.3 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr23:23748660 T>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:23740101 C>A did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr17:73949632 G>C maps to NM_004035.6 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:73945895 G>A maps to NM_004035.6 Q461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr17:73944429 G>A maps to NM_004035.6 Q613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr17:73974760 C>T maps to NM_004035.6 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr17:73947642 C>T maps to NM_004035.6 Q320Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:73974646 G>A maps to NM_004035.6 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr17:73969829 G>A maps to NM_007292.5 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr17:73949677 C>A maps to NM_004035.6 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr3:58520094 G>A maps to NM_003500.3 Y105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr3:58519787 G>C maps to NM_003500.3 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:58520680 C>T maps to NM_003500.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr4:8383275 T>C maps to NM_003501.2 K532K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:8407704 G>A maps to NM_003501.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr4:8383293 G>A maps to NM_003501.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr4:8383280 G>A maps to NM_003501.2 Q531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:8416610 G>C maps to NM_003501.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr2:111556603 C>T maps to NM_001142807.1 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr2:272113 G>A maps to NM_004300.3 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:275175 C>T maps to NM_004300.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:47267304 C>T maps to NM_001610.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr11:47261667 C>T maps to NM_001610.2 *424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr11:47266900 C>T maps to NM_001610.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr1:147124334 G>A maps to NM_016361.3 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr3:132063859 C>T maps to NM_001134194.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr3:132050576 G>A maps to NM_001134194.1 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:132063830 G>T maps to NM_001134194.1 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr3:132086581 G>A maps to NM_001134194.1 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr3:132071643 G>A maps to NM_001134194.1 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr19:51298099 C>G maps to NM_033068.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:51293712 C>G maps to NM_033068.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:51298099 C>G maps to NM_033068.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr22:51182531 C>T maps to NM_001097.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr22:51178250 G>A maps to NM_001097.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr22:51182531 C>T maps to NM_001097.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr23:70811991 C>G did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr23:70823835 G>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:70824255 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:70823545 A>G did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr23:70823809 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr23:70823810 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr23:70823741 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:6177389 C>T maps to NM_030924.3 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:6187357 G>A maps to NM_030924.3 K535K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr19:6177376 C>G maps to NM_030924.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr19:6166013 C>T maps to NM_030924.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr17:48548429 G>A maps to ENST00000427954 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:48539807 G>A maps to ENST00000427954 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr17:48538698 C>T maps to ENST00000427954 Q166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr16:89220539 G>A maps to NM_174917.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr16:89167160 G>A maps to NM_174917.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr4:185687900 G>A maps to NM_001995.2 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr4:185697724 G>A maps to NM_001995.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr4:185691609 T>C maps to NM_001995.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr23:108926499 G>A did not map to a codon.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr23:108924329 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:108921319 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:108906541 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr10:114176780 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:114136149 C>G maps to NM_016234.3 S28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr5:131322535 T>C maps to NM_001009185.1 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:131321145 C>T maps to NM_001009185.1 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr5:131323818 G>A maps to NM_001009185.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:20636752 G>A maps to NM_052956.2 R507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr16:20482433 C>T maps to NM_001010845.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr16:20481008 T>C maps to NM_001010845.2 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr16:20482505 G>A maps to NM_001010845.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr16:20554328 C>G maps to NM_182617.3 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr16:20559383 C>T maps to NM_182617.3 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr16:20552066 G>T maps to NM_182617.3 S513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr16:20576154 G>A maps to NM_182617.3 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr16:20787319 C>T maps to NM_005622.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr16:20808287 A>T maps to NM_005622.3 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr12:7473373 G>A maps to NM_001080454.1 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr12:7459280 C>T maps to NM_001080454.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr12:7470644 C>G maps to NM_001080454.1 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr16:20430711 C>G maps to NM_017888.2 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr16:20423010 G>A did not map to a codon.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr20:25000700 G>A maps to NM_032501.2 Y397Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:24994204 G>A maps to NM_032501.2 R516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr20:25038495 G>A maps to NM_032501.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr20:24994689 G>A maps to NM_032501.2 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr20:33507278 C>T maps to NM_001076552.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr20:33508912 C>G maps to NM_001076552.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr20:33509249 C>T maps to NM_001076552.2 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:81472104 C>A maps to NM_024560.2 S69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr12:81503359 C>T maps to NM_024560.2 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:81647168 C>G maps to NM_024560.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr12:81648680 G>T maps to NM_024560.2 E681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr12:81624889 C>T maps to NM_024560.2 F523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:229567792 G>T maps to NM_001100.3 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr10:90707056 C>T maps to NM_001141945.1 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr7:5569258 G>C maps to NM_001101.3 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr7:5567772 G>A maps to NM_001101.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:5569264 G>T maps to NM_001101.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr7:5568941 G>A maps to NM_001101.3 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr7:5567500 T>A maps to NM_001101.3 K336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr5:56777787 G>A maps to NM_001017992.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr15:35084756 G>A maps to NM_005159.4 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:79478271 G>A maps to NM_001614.2 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:79479014 C>A maps to NM_001614.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr17:79478045 C>T maps to NM_001614.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr17:79478099 G>A maps to NM_001614.2 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:179294031 G>A maps to NM_004301.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:100245111 C>T maps to NM_016188.4 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr7:100252641 C>T maps to NM_016188.4 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr7:100244898 G>A maps to NM_016188.4 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr7:100246436 G>A maps to NM_016188.4 N159N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:111624742 G>A maps to NM_006687.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:18152500 C>G maps to NM_030812.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:18152534 C>T maps to NM_030812.2 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr1:18149667 C>T maps to NM_030812.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:18152476 C>T maps to NM_030812.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:8808754 G>C maps to NM_178525.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr19:8808069 G>A maps to NM_178525.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr19:8808430 G>A maps to NM_178525.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:236883472 C>T maps to NM_001103.2 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:236908073 C>G maps to NM_001103.2 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:236908061 C>T maps to NM_001103.2 I464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr1:236908067 G>A maps to NM_001103.2 Q466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:66322673 C>T maps to NM_001104.1 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:66329732 G>A maps to NM_001104.1 Q776Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:39208571 C>T maps to NM_004924.3 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:39208628 G>A maps to NM_004924.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr19:39191750 C>T maps to NM_004924.3 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr14:58675797 C>T maps to NM_018477.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr14:58678051 C>T maps to NM_018477.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:104240640 G>A maps to NM_005736.3 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr10:104242806 C>T maps to NM_005736.3 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr10:104248818 C>T did not map to a codon.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:98275436 G>C maps to NM_005735.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr2:65467064 C>A maps to NM_001005386.2 S43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr7:152551554 C>T maps to NM_020445.4 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr7:152549242 C>T maps to NM_020445.4 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr7:152497629 G>T maps to NM_020445.4 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr7:149981865 G>A maps to NM_001164458.1 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr20:37394954 C>T maps to NM_024855.3 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr20:37378813 G>T maps to NM_024855.3 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr3:53910036 G>A maps to NM_022899.4 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:53905382 C>A maps to NM_022899.4 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:53904097 G>A maps to NM_022899.4 Q548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr23:127185930 C>A did not map to a codon.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr23:127185358 G>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:127185989 C>A did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:127185630 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:2939197 C>T maps to NM_080431.4 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr1:2938774 G>A maps to NM_080431.4 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:2938570 G>A maps to NM_080431.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:2938987 C>T maps to NM_080431.4 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:158626898 C>T maps to NM_001111067.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr12:52385734 G>A maps to NM_020328.3 Q491Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:158406899 T>C maps to NM_145259.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr2:148672794 T>C maps to NM_001616.3 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr2:148677882 T>G maps to NM_001616.3 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:38519698 C>T maps to NM_001106.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr12:52312838 G>A maps to NM_001077401.1 K439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:52314579 G>A maps to NM_001077401.1 W472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr3:52022982 C>T maps to ENST00000463937 H474H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr3:52020494 G>A maps to ENST00000463937 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:52020506 T>C maps to ENST00000463937 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr11:67412756 C>T did not map to a codon.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr2:54531937 A>G maps to NM_138448.3 *100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr20:43255221 G>A maps to NM_000022.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr20:43251683 G>A maps to NM_000022.2 H214H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr20:43264905 G>A maps to NM_000022.2 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr20:43251677 C>A maps to NM_000022.2 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr4:123317467 A>G maps to NM_139243.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr4:123304954 T>A maps to NM_139243.3 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr4:123332469 C>G maps to NM_139243.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr4:123342481 T>C maps to NM_139243.3 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr16:84229910 C>G maps to NM_139174.3 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr15:58936129 G>A maps to NM_001110.2 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr17:42857109 C>A maps to NM_002390.4 S766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr17:42855098 G>C maps to NM_002390.4 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr17:42850283 C>T maps to NM_002390.4 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:42850645 C>G maps to NM_002390.4 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:42849818 G>C maps to NM_002390.4 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr17:42855381 C>T maps to NM_002390.4 I711I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr17:42850645 C>G maps to NM_002390.4 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr17:42849016 C>G maps to NM_002390.4 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr17:42848992 G>A maps to NM_002390.4 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr17:42847156 G>A maps to NM_002390.4 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr10:127737959 G>C maps to NM_003474.4 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr10:127824154 G>A maps to NM_003474.4 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr10:128018998 C>T maps to NM_003474.4 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:127755327 C>T maps to NM_003474.4 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr1:155029460 C>A maps to NM_207197.1 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr1:155025186 G>A maps to NM_207197.1 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:9695719 G>A maps to NM_003183.4 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr2:9637282 G>A maps to NM_003183.4 F581F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr2:9663423 G>C maps to NM_003183.4 S266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:9663467 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr8:39537619 C>T maps to NM_014237.2 Q566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr8:39468068 T>C maps to NM_014237.2 N122N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:156932735 A>G maps to ENST00000430702 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr5:156946864 G>T maps to ENST00000430702 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr5:156920124 G>A maps to ENST00000430702 N590N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr5:156997911 C>T maps to ENST00000430702 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr5:156915419 C>T maps to ENST00000430702 G803G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:39604117 T>A maps to NM_001464.3 K683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr8:39627031 G>C maps to NM_001464.3 S364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr8:39644566 C>A maps to NM_001464.3 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:70989716 G>A maps to NM_003814.4 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr14:70991612 G>A maps to NM_003814.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr14:70926036 G>A maps to NM_003813.2 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr14:70925821 C>T maps to NM_003813.2 Q536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr7:87762244 G>A maps to NM_021723.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr7:87743931 C>G maps to NM_021723.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr7:87564470 G>C maps to NM_021723.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:87757966 G>C maps to NM_021723.3 L243L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-ZF-A9RG-01A-21D-A42E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr7:87762244 G>A maps to NM_021723.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:207310118 C>T maps to NM_003812.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:207310143 G>T maps to NM_003812.2 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr2:207345996 C>T maps to NM_003812.2 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr2:207457380 C>T maps to NM_003812.2 R667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr2:207408039 G>A maps to NM_003812.2 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:207424806 C>T maps to NM_003812.2 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:24178762 C>T maps to NM_014265.4 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr4:175899048 G>A maps to NM_014269.4 T791T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr4:175896927 A>T maps to NM_014269.4 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr4:175898899 C>T maps to NM_014269.4 Q742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr4:175899001 C>T maps to NM_014269.4 Q776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr4:175898919 C>A maps to NM_014269.4 S748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr4:175898027 C>G maps to NM_014269.4 S451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr4:175899040 C>T maps to NM_014269.4 Q789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr4:175899007 C>T maps to NM_014269.4 Q778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:120438389 C>T maps to NM_021794.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr1:120436732 C>A maps to NM_021794.2 E743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr1:120438647 A>T maps to NM_021794.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr8:39044507 C>T maps to NM_145004.5 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr8:24324309 A>C did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr8:38869205 A>G maps to NM_003816.2 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:24261574 C>T maps to NM_014479.3 C460C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr21:28214228 G>A maps to NM_006988.3 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr21:28210347 T>C maps to NM_006988.3 K818K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:8661944 C>T maps to NM_030957.2 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr19:8651501 C>T maps to NM_030957.2 G781G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr19:8670213 C>A maps to NM_030957.2 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr19:8665901 G>A maps to NM_030957.2 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr19:8665874 C>T maps to NM_030957.2 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr19:8665954 C>A maps to NM_030957.2 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr5:33535052 T>C maps to NM_030955.2 Q1497Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr5:33576734 G>A maps to NM_030955.2 S1132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:33641931 C>T maps to NM_030955.2 R567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:33751569 C>T maps to NM_030955.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr5:33649672 G>A maps to NM_030955.2 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr5:33588859 C>T maps to NM_030955.2 E903E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:33596061 G>T maps to NM_030955.2 C877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr5:33683978 G>A maps to NM_030955.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr5:33658335 A>G maps to NM_030955.2 D381D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:33751584 C>T maps to NM_030955.2 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr5:33577064 G>T maps to NM_030955.2 V1022V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr9:136324272 C>T maps to NM_139025.3 Q1419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr9:136295081 G>A maps to NM_139025.3 W283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr9:136323080 G>A maps to NM_139025.3 S1314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr9:136324256 G>A maps to NM_139025.3 P1413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr10:72434640 G>T maps to NM_139155.2 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr10:72496494 C>T maps to NM_139155.2 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr10:72520584 C>T maps to NM_139155.2 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr10:72513660 G>A maps to NM_139155.2 K948K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr11:130318900 C>T maps to NM_139055.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:130319038 C>T maps to NM_139055.2 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr11:130343076 C>T maps to NM_139055.2 N738N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr5:5303688 C>G maps to NM_139056.2 S999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr5:5190224 G>T maps to NM_139056.2 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:5239962 C>T maps to NM_139056.2 F816F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:5239386 C>T maps to NM_139056.2 Q760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:5239992 G>A maps to NM_139056.2 E826E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:5182251 G>A maps to NM_139056.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr5:5146313 C>T maps to NM_139056.2 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr5:5186226 C>A maps to NM_139056.2 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr5:5303689 A>C maps to NM_139056.2 S999S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr5:5239962 C>T maps to NM_139056.2 F816F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr5:5182155 G>T did not map to a codon.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr5:5303785 C>T maps to NM_139056.2 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr5:5232614 C>G maps to NM_139056.2 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr5:5239830 G>A maps to NM_139056.2 R772R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr15:100692855 G>A maps to NM_139057.2 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr15:100801781 C>T maps to NM_139057.2 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr15:100673516 G>A maps to NM_139057.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr15:100692957 G>C maps to NM_139057.2 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr15:100821442 G>A maps to NM_139057.2 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr15:100636624 G>A maps to NM_139057.2 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr16:77317891 G>A maps to NM_199355.2 Y1209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:77353979 C>T maps to NM_199355.2 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr16:77387775 G>A maps to NM_199355.2 Q490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr16:77465224 G>A maps to NM_199355.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr16:77465474 G>C maps to NM_199355.2 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr16:77328939 C>T maps to NM_199355.2 K962K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr5:128863478 G>A maps to NM_133638.3 Q369Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:128994395 C>A maps to NM_133638.3 I791I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:129019955 T>A maps to NM_133638.3 T930T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr5:129040002 C>G maps to NM_133638.3 V1071V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr5:128983543 A>T maps to NM_133638.3 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr5:129030531 C>T maps to NM_133638.3 Q974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr5:128844786 C>G maps to NM_133638.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr5:178553117 G>A maps to NM_014244.4 T877T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:178554963 G>A maps to NM_014244.4 G871G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:178553051 C>T maps to NM_014244.4 S899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:178580518 G>A maps to NM_014244.4 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr5:178552181 C>A did not map to a codon.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr5:178579178 C>T maps to NM_014244.4 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr12:43826584 G>T maps to ENST00000389420 S917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr12:43822322 G>A maps to ENST00000389420 S1222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:43944995 G>A maps to ENST00000389420 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr12:43945691 G>C maps to ENST00000389420 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr12:43833792 T>C maps to ENST00000389420 Q790Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr4:73149067 G>A maps to NM_014243.1 Q1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:161166036 G>A maps to NM_005099.4 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr1:161167829 G>A maps to NM_005099.4 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:161167937 G>A maps to NM_005099.4 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr21:28302317 C>T maps to NM_007038.3 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr21:28296647 G>T maps to NM_007038.3 P839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr21:28338461 G>C maps to NM_007038.3 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr21:28296383 C>T maps to NM_007038.3 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr21:28327085 G>A maps to NM_007038.3 H403H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr5:64629867 C>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr5:64769401 A>T did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr5:64748713 C>T maps to NM_197941.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr15:79058073 C>T maps to ENST00000258883 P1393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr15:79063929 G>A maps to ENST00000258883 I791I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr15:79058040 G>T maps to ENST00000258883 P1404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr15:79059348 G>T maps to ENST00000258883 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:130275494 G>A maps to NM_007037.4 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr11:130275533 G>A maps to NM_007037.4 S863S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr11:130275619 G>A maps to NM_007037.4 Q835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:64554055 G>A maps to NM_182920.1 G1504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr3:64589990 G>T maps to NM_182920.1 S1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr3:64617493 T>C maps to NM_182920.1 T761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr3:64627624 G>A maps to NM_182920.1 P585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr3:64617146 G>A maps to NM_182920.1 D791D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr3:64619153 A>C maps to NM_182920.1 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr3:64619472 G>A maps to NM_182920.1 R647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr3:64547316 C>A maps to NM_182920.1 S1545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr3:64636745 G>A maps to NM_182920.1 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr3:64617152 T>C maps to NM_182920.1 E789E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr9:18504837 C>A maps to NM_001040272.4 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr9:18635940 C>A maps to NM_001040272.4 S201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr9:136402606 G>A maps to ENST00000393061 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr9:136402525 G>A did not map to a codon.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr9:136409599 C>T maps to ENST00000393061 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr15:84700133 C>T maps to NM_207517.2 H1568H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr15:84560116 C>T maps to NM_207517.2 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:84651604 G>A maps to NM_207517.2 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr15:84581958 G>T maps to NM_207517.2 E606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr15:84611708 C>T maps to NM_207517.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr15:84700185 T>G did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr15:84506896 C>T maps to NM_207517.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr15:84581894 G>T maps to NM_207517.2 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr15:84553885 C>T maps to NM_207517.2 Q332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:150532596 C>T maps to ENST00000369039 V1073V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr1:150532262 G>A maps to ENST00000369039 T1013T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr1:150532590 C>T maps to ENST00000369039 L1071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr7:938745 C>T maps to NM_006869.2 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:29276306 G>A maps to ENST00000394782 E226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr17:29280325 G>A maps to ENST00000394782 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:154573728 C>T maps to ENST00000292205 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr1:154574976 G>C maps to ENST00000292205 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr21:46596308 G>A maps to NM_015833.3 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr21:46624532 G>A maps to NM_015833.3 S583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr10:1405297 G>A maps to NM_018702.2 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr10:1230815 C>T maps to NM_018702.2 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr10:1229216 C>T maps to NM_018702.2 Q712Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr10:1779281 C>T maps to NM_018702.2 K21K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr16:75654167 C>T maps to NM_012091.3 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:75646148 C>T maps to NM_012091.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr16:75654568 T>A maps to NM_012091.3 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr14:78325483 G>A maps to NM_020421.3 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr14:78397943 C>G maps to NM_020421.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr14:78392225 G>A maps to NM_020421.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr7:140373534 G>A maps to NM_052853.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr7:140373324 G>A maps to NM_052853.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:41206058 C>T maps to NM_024876.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr19:41220197 C>T maps to NM_024876.3 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr8:145616823 G>A maps to NM_174922.3 E281E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr7:45743203 C>G maps to NM_021116.2 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr7:45726196 C>G maps to NM_021116.2 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr7:45726144 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr7:45719326 C>T maps to NM_021116.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr1:167792258 G>T maps to NM_018417.4 I1385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:167849780 G>A maps to NM_018417.4 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr1:167802337 G>A maps to NM_018417.4 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:167779022 G>A maps to NM_018417.4 I1575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:167805567 G>A maps to NM_018417.4 L1096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:167849835 G>A maps to NM_018417.4 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr5:7520876 C>T maps to NM_020546.2 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr5:7817055 C>T maps to NM_020546.2 I987I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:7773073 G>A maps to NM_020546.2 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr5:7396423 G>A maps to NM_020546.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr5:7789894 C>A maps to NM_020546.2 A870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr5:7626357 C>T maps to NM_020546.2 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:7789837 G>A maps to NM_020546.2 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr5:7520894 G>A maps to NM_020546.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr5:7773124 C>T maps to NM_020546.2 I765I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr5:7695948 C>G maps to NM_020546.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr5:7804696 G>T did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr5:7784498 G>A maps to NM_020546.2 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr5:7743779 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:25047258 C>T maps to NM_004036.3 K908K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr2:25141526 C>G maps to NM_004036.3 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr2:25042932 C>A maps to NM_004036.3 V1101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:24801005 C>T maps to NM_139247.3 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr14:24801041 G>T maps to NM_139247.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr14:24800295 G>A maps to NM_139247.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr14:24802089 C>T maps to NM_139247.3 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr3:123166413 C>A maps to NM_183357.2 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr3:123005624 C>T maps to NM_183357.2 V1188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr3:123019118 G>A maps to NM_183357.2 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:123046524 G>A maps to NM_183357.2 N629N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:123014972 C>T maps to NM_183357.2 Q1007Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr3:123021997 G>A maps to NM_183357.2 V876V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr3:123036883 C>T maps to NM_183357.2 Q779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:123166690 G>A maps to NM_183357.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:123166642 C>T maps to NM_183357.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:49170015 G>A maps to NM_015270.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr12:49171949 G>A maps to NM_015270.3 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr12:49177001 C>T maps to NM_015270.3 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:50346029 G>A maps to NM_001114.3 V844V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr16:50332876 C>T maps to NM_001114.3 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:50339494 G>A maps to NM_001114.3 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:50339738 G>A maps to NM_001114.3 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr16:50339458 C>T maps to NM_001114.3 D547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr16:50346847 C>T maps to NM_001114.3 S884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:131812677 G>A maps to NM_001115.2 F1018F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr8:132051645 G>T maps to NM_001115.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr8:131795949 A>G maps to NM_001115.2 F1085F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr8:132002782 C>T maps to NM_001115.2 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr8:132051979 G>A maps to NM_001115.2 H200H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr8:131955662 G>C maps to NM_001115.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr16:4016693 C>T maps to NM_001116.3 Q1048Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr16:4016705 C>T maps to NM_001116.3 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:4027574 G>A maps to NM_001116.3 F912F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:4016705 C>T maps to NM_001116.3 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr16:4042322 G>A maps to NM_001116.3 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:31126104 C>T maps to ENST00000409489 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:31126557 G>A maps to ENST00000409489 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr7:31123786 G>A maps to ENST00000409489 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr4:2930072 C>T maps to NM_014189.2 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr4:2916621 G>C maps to NM_014189.2 V570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr4:2927795 G>T maps to NM_014189.2 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr4:2906528 G>A maps to NM_014189.2 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr4:2877806 G>A maps to NM_014189.2 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:2900170 C>G maps to NM_014189.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr4:2899987 C>G maps to NM_014189.2 Y273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr4:2877837 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr4:2910283 C>T maps to NM_014189.2 Q551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr2:70905849 G>A maps to NM_001185054.1 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr2:70903918 C>T maps to NM_001185055.1 Q550Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:111881974 G>A maps to NM_016824.3 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr10:111892132 G>A maps to NM_016824.3 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr10:111878394 G>A maps to NM_016824.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr10:111883998 G>A maps to NM_016824.3 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr4:100237198 G>A maps to NM_000668.4 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr4:100235051 G>A maps to NM_000668.4 Q252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr4:100237180 G>A maps to NM_000668.4 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:100047779 G>A maps to ENST00000505590 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr4:100048495 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr8:67369108 C>A maps to NM_144650.2 Y348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:3504728 G>A maps to NM_018269.3 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr20:37214717 G>A maps to ENST00000416116 W38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr20:37209988 C>T maps to ENST00000416116 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr3:186572144 C>T maps to NM_004797.3 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:202911286 C>A maps to NM_015999.3 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr12:1893112 C>T maps to NM_024551.2 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr12:1893166 C>G maps to NM_024551.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:1895204 C>T maps to NM_024551.2 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr11:10328160 G>A maps to NM_001124.1 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:50921130 C>T maps to NM_024866.4 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr20:49508271 T>C maps to NM_181442.1 P993P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr20:49510908 G>A maps to NM_181442.1 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr18:77894027 G>A maps to NM_014913.3 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr18:77895029 G>C maps to NM_014913.3 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr18:77895770 C>T maps to NM_014913.3 F825F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr10:64564917 C>G maps to NM_032804.5 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:24837151 G>T maps to NM_000675.4 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr22:24836863 C>T maps to NM_000675.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr22:24837357 C>T maps to NM_000675.4 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:119306403 G>T maps to NM_001125.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr3:119305345 G>A maps to NM_001125.2 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr13:114077229 G>A maps to NM_138430.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr13:114077229 G>A maps to NM_138430.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr13:114077229 G>A maps to NM_138430.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr1:36557422 G>A maps to NM_017825.2 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr1:36557422 G>A maps to NM_017825.2 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:26628124 G>A maps to ENST00000356368 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr8:26722360 C>T maps to ENST00000356368 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr8:26722393 C>T maps to ENST00000356368 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr8:26722054 G>A maps to ENST00000356368 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr8:26722153 G>A maps to ENST00000356368 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr5:159344796 G>A maps to NM_000679.3 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr20:4202243 C>A maps to NM_000678.3 E549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr20:4228878 G>A maps to NM_000678.3 D242D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:112839121 C>T maps to NM_000681.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr10:112838905 G>A maps to NM_000681.3 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:96780655 G>A maps to NM_000682.5 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr2:96781354 G>A maps to NM_000682.5 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr2:96780784 G>A maps to NM_000682.5 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:3768989 C>T maps to NM_000683.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr4:3768848 C>T maps to NM_000683.3 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr10:115804343 C>T maps to NM_000684.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr10:115804452 C>T maps to NM_000684.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr10:115804496 G>A maps to NM_000684.2 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:148206576 C>T maps to NM_000024.5 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr5:148206978 G>A maps to NM_000024.5 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:67051767 C>T maps to NM_001619.3 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:67052908 C>T maps to NM_001619.3 A686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr11:67051207 C>T maps to NM_001619.3 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr11:67049329 C>T maps to NM_001619.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr11:67052450 C>T maps to NM_001619.3 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:26110490 C>T maps to NM_005160.3 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr20:60881303 C>T maps to NM_175573.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr20:60882814 C>T maps to NM_175573.1 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr20:60883122 C>T maps to NM_175573.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr20:60878629 G>A maps to NM_175573.1 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr20:60878722 G>A maps to NM_175573.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr20:60881752 C>A maps to NM_175573.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:244587307 C>A maps to NM_001126.3 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr7:44152473 C>T maps to NM_001129.3 I845I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr7:44151898 C>T maps to NM_001129.3 R732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr7:44151552 C>T maps to NM_001129.3 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:19593294 C>A maps to NM_001114176.1 S221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr15:89172608 G>A maps to NM_022767.3 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr4:7840264 C>A maps to NM_001134647.1 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr4:7774714 C>A maps to NM_001134647.1 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr4:7870359 G>A maps to NM_001134647.1 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr4:7840337 C>T maps to NM_001134647.1 K213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr4:7811406 G>A maps to NM_001134647.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr4:7820892 G>A maps to NM_001134647.1 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr4:7817743 C>T did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr10:116061126 C>A maps to NM_001001936.1 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr4:88048266 C>T maps to NM_001166693.1 D967D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr4:88055793 T>C maps to NM_001166693.1 L1161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:88036294 G>A maps to NM_001166693.1 V770V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr4:88048242 A>G maps to NM_001166693.1 P959P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr4:88036056 C>G maps to NM_001166693.1 S691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr23:147743711 C>G did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:148037677 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:148037318 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:147919172 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:148044243 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr23:147743504 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:147733646 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr23:148048407 T>C did not map to a codon.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr23:148055006 A>C did not map to a codon.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr23:148069075 G>C did not map to a codon.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr23:147743989 G>C did not map to a codon.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr23:148072789 C>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:147733615 T>C did not map to a codon.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr23:148035155 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:147733628 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr23:147743902 G>C did not map to a codon.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr23:148037965 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:148037188 A>G did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr23:148068995 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr23:148037369 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr23:148059510 G>T did not map to a codon.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr2:100167950 G>A maps to NM_001025108.1 S1247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr2:100623171 C>T maps to NM_001025108.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr2:100623237 C>T maps to NM_001025108.1 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:100209920 G>A maps to NM_001025108.1 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr2:100170934 G>A maps to NM_001025108.1 Q1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr2:100623270 G>A maps to NM_001025108.1 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr2:100209851 T>C maps to NM_001025108.1 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr2:100209752 G>A maps to NM_001025108.1 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr2:100360566 T>G maps to NM_001025108.1 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr5:132219227 A>G maps to NM_014423.3 P1056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:132223558 G>C maps to NM_014423.3 S971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:132270502 G>C maps to NM_014423.3 S85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr18:12367071 G>C maps to NM_006796.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr4:74363403 C>G maps to NM_001133.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr4:74364926 T>C maps to NM_001133.2 C462C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr17:76202999 G>A maps to NM_001145526.1 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr17:76183501 G>A maps to NM_001145526.1 K17K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:64796343 C>T maps to ENST00000422803 R736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr2:64779057 C>T maps to ENST00000422803 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:64779142 C>T maps to ENST00000422803 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:178352918 G>A maps to NM_000027.3 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:236617865 C>T maps to NM_001037131.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr2:236653472 G>A maps to NM_001037131.1 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:236649650 C>T maps to NM_001037131.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:237029081 C>T maps to NM_001037131.1 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr10:88768839 T>A maps to NM_133447.1 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:58124278 C>T maps to NM_001122772.1 T809T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr12:58131090 G>T maps to NM_001122772.1 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr12:58124613 G>A maps to NM_001122772.1 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:58127920 G>A maps to NM_001122772.1 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:58135767 G>C maps to NM_014770.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr12:58124284 G>A maps to NM_001122772.1 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr12:58120984 G>C maps to NM_001122772.1 A1036A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr12:58124374 G>A maps to NM_001122772.1 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr12:58124377 T>C maps to NM_001122772.1 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:150814757 C>T maps to NM_031946.4 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr7:150784082 C>T maps to NM_031946.4 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr7:150817138 C>T maps to NM_031946.4 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr7:150837087 C>G maps to NM_031946.4 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:150835351 C>T maps to NM_031946.4 Q540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr7:150820942 C>T maps to NM_031946.4 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr10:46322049 C>T maps to ENST00000355953 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:75434491 G>A maps to NM_001144000.1 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr10:75457453 T>C maps to NM_001144000.1 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr10:75457465 C>T maps to NM_001144000.1 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr10:51465270 G>T maps to ENST00000416142 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr10:51465357 G>A maps to ENST00000416142 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr15:87066136 C>G maps to NM_152336.2 L838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr15:87217599 C>T maps to NM_152336.2 Q1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr15:86790935 C>T maps to NM_152336.2 Y141Y. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-K4-A5RH-01A-11D-A30E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr15:86940687 C>T maps to NM_152336.2 V776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:47689239 C>T maps to ENST00000357610 Q743Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:27279540 C>T maps to NM_021831.5 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:32150063 G>A maps to ENST00000375070 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr6:32151708 C>T maps to ENST00000375070 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr7:100151097 C>G maps to NM_006076.4 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr7:100151720 C>T maps to NM_006076.4 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr7:100151732 C>T maps to NM_006076.4 H201H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr5:76326728 C>T maps to NM_018046.4 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr5:76335495 G>A maps to NM_018046.4 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr7:141352722 G>A maps to NM_018238.3 *423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:141349061 G>C did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:100366353 C>G maps to ENST00000311030 L1176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr1:100336088 C>T maps to ENST00000311030 Y267Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:100340915 A>G maps to ENST00000311030 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr1:100379278 C>T maps to ENST00000311030 T1383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:100330037 C>G maps to ENST00000311030 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr6:32138225 G>A maps to NM_032741.4 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr6:32138788 G>A maps to NM_032741.4 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr9:139571567 C>A maps to NM_006412.3 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr21:45390598 G>A maps to NM_001037553.1 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr21:45389126 G>A maps to NM_001037553.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr21:45379720 C>T maps to NM_001037553.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr6:161560578 C>T maps to NM_020133.2 W306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr8:41476219 C>T maps to NM_178819.3 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr8:41476310 C>T maps to NM_178819.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr8:41466952 G>T maps to NM_178819.3 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr4:84457879 C>G maps to NM_032717.3 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:178299081 A>C maps to NM_003659.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr2:178362474 A>G maps to NM_003659.3 K448K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:178364366 C>T maps to NM_003659.3 Q462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr2:178378610 C>T maps to NM_003659.3 Q558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:16840962 G>A maps to ENST00000223274 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:16841375 G>C maps to ENST00000223274 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:16839411 C>A maps to ENST00000223274 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr7:16834566 T>C maps to ENST00000223274 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr7:16901636 G>A maps to NM_176813.3 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr7:16899205 T>G maps to NM_176813.3 *167Y. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-GU-A42R-01A-11D-A23M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:957837 G>A maps to NM_198576.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr1:976685 C>T maps to NM_198576.2 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr1:979600 C>G maps to NM_198576.2 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:979600 C>T maps to NM_198576.2 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr1:230839994 G>A maps to NM_000029.3 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:230845939 C>T maps to NM_000029.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:230845795 C>A maps to NM_000029.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr9:88272366 G>A maps to ENST00000395847 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr9:88257813 T>C maps to ENST00000395847 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:88247958 G>A maps to ENST00000395847 Q545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:88207607 G>C maps to ENST00000395847 S812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr9:88204597 T>C did not map to a codon.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr3:148459500 G>T maps to NM_032049.2 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr3:148459079 C>T maps to NM_032049.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr3:148459511 G>A maps to NM_032049.2 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:115304524 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:115303665 G>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:115303993 G>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr23:115304053 C>T did not map to a codon.
Multiple mappings detected for codon TCGA-4Z-AA7Y-01A-11D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr1:11808648 G>T maps to NM_020350.4 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr2:241808419 C>A maps to NM_000030.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:35047970 C>T maps to NM_031900.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr5:35003954 C>T maps to NM_031900.3 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr5:177640079 C>G maps to NM_153373.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:177658430 G>A maps to NM_153373.2 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr5:177656981 G>C maps to NM_153373.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr1:247025299 T>A maps to ENST00000428671 S1270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr1:247040278 C>G maps to ENST00000428671 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr20:32880236 G>A maps to NM_000687.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr20:32868840 C>A maps to NM_000687.2 *433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr20:32878391 G>A maps to NM_000687.2 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:110555026 G>A maps to NM_006621.4 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:110527763 C>T maps to NM_006621.4 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:110559288 C>T maps to NM_006621.4 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr7:129028912 T>C maps to NM_015328.3 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:27876121 G>C maps to NM_001029882.2 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr1:27875892 G>A maps to NM_001029882.2 Q912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:27874135 G>A maps to NM_001029882.2 A1497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr1:27873907 C>T maps to NM_001029882.2 A1573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr6:135726114 C>A maps to NM_017651.4 E988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr6:135787123 G>A maps to NM_017651.4 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr11:62289476 G>A maps to NM_001620.1 L4138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr11:62288748 G>A maps to NM_001620.1 I4380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr11:62289300 G>A maps to NM_001620.1 F4196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr11:62286723 G>C maps to NM_001620.1 L5055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr11:62288124 G>A maps to NM_001620.1 L4588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr11:62298415 G>C maps to NM_001620.1 S1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr11:62289474 C>G maps to NM_001620.1 L4138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:62288784 G>C maps to NM_001620.1 L4368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:62297472 T>C maps to NM_001620.1 T1472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:62295135 G>A maps to NM_001620.1 F2251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr11:62288916 G>A maps to NM_001620.1 F4324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr11:62289516 G>A maps to NM_001620.1 L4124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr11:62299875 G>A maps to NM_001620.1 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:62301533 C>A maps to NM_001620.1 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr11:62289258 C>T maps to NM_001620.1 V4210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr11:62285469 G>C maps to NM_001620.1 G5473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr11:62284896 G>T maps to NM_001620.1 P5664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr11:62293740 C>T maps to NM_001620.1 L2716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:62292549 C>A maps to NM_001620.1 L3113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr11:62297676 C>G maps to NM_001620.1 V1404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:62286150 C>T maps to NM_001620.1 V5246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:62295615 C>G maps to NM_001620.1 V2091V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:62297075 C>A maps to NM_001620.1 E1605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr11:62289684 G>A maps to NM_001620.1 F4068F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:62297733 C>T maps to NM_001620.1 V1385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr11:62287596 G>A maps to NM_001620.1 I4764I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr11:62285505 C>G maps to NM_001620.1 V5461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr11:62293818 C>T maps to NM_001620.1 L2690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr14:105413507 C>T maps to NM_138420.2 L2760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr14:105414539 G>C maps to NM_138420.2 L2416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr14:105409409 C>T maps to NM_138420.2 V4126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr14:105412790 G>A maps to NM_138420.2 V2999V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr14:105408254 G>T maps to NM_138420.2 L4511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:105410847 G>T maps to NM_138420.2 S3647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:105415177 G>A maps to NM_138420.2 Q2204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:105415184 G>A maps to NM_138420.2 L2201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:105410000 A>G maps to NM_138420.2 V3929V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr14:105419746 T>A maps to NM_138420.2 K681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:105420746 C>T maps to NM_138420.2 Q347Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr14:105410234 G>T maps to NM_138420.2 L3851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr14:105410636 G>C maps to NM_138420.2 L3717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr14:105416414 C>T maps to NM_138420.2 V1791V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr14:105411797 C>A maps to NM_138420.2 S3330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr14:105417962 C>G maps to NM_138420.2 L1275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr14:105406883 C>T maps to NM_138420.2 K4968K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr14:105411521 G>A maps to NM_138420.2 V3422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr14:105419486 C>T maps to NM_138420.2 K767K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr14:105408167 G>A maps to NM_138420.2 A4540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr14:105413132 G>A maps to NM_138420.2 H2885H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr14:105413150 C>T maps to NM_138420.2 V2879V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr14:105412757 G>A maps to NM_138420.2 A3010A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr14:105411428 C>T maps to NM_138420.2 A3453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr14:105413204 G>A maps to NM_138420.2 I2861I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr14:105411602 C>T maps to NM_138420.2 E3395E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr14:105412769 C>T maps to NM_138420.2 P3006P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr14:105409259 G>C maps to NM_138420.2 L4176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr14:105414023 G>C maps to NM_138420.2 V2588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr14:105418736 G>T maps to NM_138420.2 I1017I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr7:17382622 C>T maps to NM_001621.4 Q828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr7:17378910 G>T maps to NM_001621.4 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr7:17367466 C>T maps to NM_001621.4 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr7:17382604 C>T maps to NM_001621.4 Q822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr7:17369592 G>A maps to NM_001621.4 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr7:17378975 G>A maps to NM_001621.4 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr5:428076 G>C maps to NM_020731.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr3:186335075 C>T maps to ENST00000273784 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:31539924 G>A maps to NM_016633.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr12:8758000 G>A maps to NM_020661.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr12:8757468 G>A maps to NM_020661.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr12:8759523 G>A maps to NM_020661.2 Y31Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr6:31584598 G>C maps to NM_001623.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr9:133993209 G>A maps to NM_001185095.1 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr23:129270625 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr23:129281743 G>T did not map to a codon.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr23:129281527 G>A did not map to a codon.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr23:129281475 T>C did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:129281743 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:129281847 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr22:21334410 G>A maps to NM_144704.2 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr6:143458087 G>A maps to NM_016108.2 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr6:106969161 C>G maps to NM_001624.2 S952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:107011685 T>G maps to NM_001624.2 S1654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr6:106969024 C>T maps to NM_001624.2 F906F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr6:107003711 T>C maps to NM_001624.2 C1477C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:159043055 T>C maps to NM_004833.1 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr1:159038363 A>G maps to NM_004833.1 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr4:107249296 G>A maps to NM_001142416.1 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr4:107268794 G>A maps to NM_001142416.1 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr7:6054920 C>T maps to NM_006303.3 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr11:67250679 G>A maps to NM_003977.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr11:67250652 C>G maps to NM_003977.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr11:67257845 C>T maps to NM_003977.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr17:6330311 C>T maps to NM_014336.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr17:6329130 G>T maps to NM_014336.3 Y268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr21:45706894 G>A maps to NM_000383.2 K114K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:4772145 G>A maps to NM_018836.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:4832501 C>T maps to NM_018836.3 C360C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr9:130630319 G>A maps to ENST00000223836 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:33490111 C>T maps to NM_001625.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr1:33486987 C>T maps to NM_001625.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:33480152 G>A maps to NM_001625.3 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:4718471 G>A maps to NM_016282.3 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr9:4722581 G>A maps to NM_016282.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr1:77987618 C>T maps to NM_174858.1 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:77763320 G>T maps to NM_174858.1 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:77987618 C>T maps to NM_174858.1 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr1:77806201 G>A maps to NM_174858.1 Q280Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:96912856 G>C maps to NM_152327.2 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:96912868 C>T maps to NM_152327.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:96944838 G>A maps to NM_152327.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr14:96953299 G>A maps to NM_152327.2 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr14:96858544 G>A maps to NM_152327.2 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr14:96909098 A>T maps to NM_152327.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47W-01A-11D-A23U-08 chr17:55197639 G>A maps to ENST00000427138 E931E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr17:55195740 G>T did not map to a codon.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr17:55184151 C>T maps to ENST00000427138 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr17:19845218 C>T maps to NM_007202.2 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr13:42877891 C>T maps to NM_016248.2 S1670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr13:42876627 C>G maps to NM_016248.2 S1249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr13:42876197 C>T maps to NM_016248.2 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:151672225 G>A maps to NM_005100.3 T900T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:151673974 G>A maps to NM_005100.3 S1483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr6:151673297 C>T maps to NM_005100.3 L1258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr6:151671703 C>T maps to NM_005100.3 D726D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:151674730 A>G maps to NM_005100.3 Q1735Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr15:86064774 C>T maps to NM_006738.4 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr15:86261371 C>A maps to NM_006738.4 R1999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr15:86123758 A>T maps to NM_006738.4 T820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr15:86273897 T>A maps to NM_006738.4 A2418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr15:86087000 A>G did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr15:86124721 G>A maps to NM_006738.4 V1141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:86123986 T>C maps to NM_006738.4 S896S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr15:86087180 A>G maps to NM_006738.4 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr15:86125000 C>G maps to NM_006738.4 V1234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr15:86266525 G>A maps to NM_006738.4 L2244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr15:86189172 C>T maps to NM_006738.4 I1454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr15:86064768 G>A maps to NM_006738.4 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:119048715 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr9:112930770 C>T maps to NM_007203.4 N1102N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr12:4735735 G>A maps to NM_006422.2 Q778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr12:4736333 A>T maps to NM_006422.2 I578I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr23:49957476 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr23:49957630 A>C did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr23:49958592 G>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr23:49962218 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:49957407 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr14:33015865 G>A maps to NM_004274.4 W669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr14:33165193 A>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:33015287 G>T maps to NM_004274.4 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:33293275 C>A maps to NM_004274.4 S2086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr14:33291558 C>T maps to NM_004274.4 Q1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr14:33290990 C>T maps to NM_004274.4 L1324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr14:33291374 C>T maps to NM_004274.4 D1452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr14:33015562 G>A maps to NM_004274.4 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:33293679 A>T maps to NM_004274.4 R2221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr14:33292499 C>T maps to NM_004274.4 G1827G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr6:131490372 G>A maps to ENST00000431975 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr6:131486246 G>A maps to ENST00000431975 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr19:15483850 C>T maps to NM_005858.2 W224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:15512113 G>C maps to NM_014371.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr19:15508029 G>C maps to NM_014371.2 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr19:15510177 C>T maps to NM_014371.2 K364K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:15508412 C>T maps to NM_014371.2 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:91631615 T>C maps to NM_005751.4 T795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr7:91667731 G>A did not map to a codon.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr7:91715573 C>T maps to NM_005751.4 F3019F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr7:91603050 T>C maps to NM_005751.4 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr7:91708502 C>G maps to NM_005751.4 L2352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr7:91709462 C>G maps to NM_005751.4 L2672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr7:91726365 G>T maps to NM_005751.4 E3365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr7:91726007 G>A maps to NM_005751.4 L3245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:91659277 G>C maps to NM_005751.4 V1406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr7:91731954 C>T maps to NM_005751.4 L3715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:91690590 G>A maps to NM_005751.4 V1873V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr7:91660845 G>A maps to NM_005751.4 V1422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr6:109980579 G>A maps to NM_001145128.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr6:109962786 T>G maps to NM_001145128.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr6:109854612 T>C maps to NM_001145128.2 G1137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr6:109965891 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:88387649 C>A maps to NM_018064.3 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr9:117108960 G>A maps to NM_030767.4 R1168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr9:117119168 A>G maps to NM_030767.4 T940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr1:109380189 G>A maps to NM_152763.3 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:109366067 C>T maps to NM_152763.3 Q697Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr1:109373224 C>G maps to NM_152763.3 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:109394827 T>C maps to NM_152763.3 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:46034628 C>T maps to NM_153326.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:46027484 C>T maps to NM_153326.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr7:134222983 C>T maps to NM_020299.4 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr7:134254235 G>C maps to ENST00000418096 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:5009207 C>T maps to NM_001353.5 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr10:5037997 G>A maps to NM_001354.4 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr10:4889678 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr10:4883977 G>T maps to NM_001040177.1 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr1:19630775 A>G maps to NM_003689.2 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:19595154 C>A maps to NM_201252.3 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr14:105243077 G>T maps to NM_001014432.1 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr14:105242099 G>A maps to NM_001014432.1 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr14:105239647 C>G maps to NM_001014432.1 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr19:50375146 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr1:243675655 G>A maps to NM_005465.3 Q442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr1:243668580 T>C maps to NM_005465.3 Q470Q. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-A6AW-01A-11D-A30E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:243716086 G>A maps to NM_005465.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr16:53526353 G>A maps to ENST00000425875 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:116152708 C>G maps to ENST00000277315 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:52245347 G>C maps to ENST00000441729 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr3:52248034 G>C did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr3:52245380 C>T maps to ENST00000441729 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr3:52245497 C>A maps to ENST00000441729 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:52245380 C>T maps to ENST00000441729 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr23:55054210 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:55051211 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr23:55042021 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr23:55050274 G>A did not map to a codon.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr23:55052285 G>C did not map to a codon.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr23:55047546 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr4:74285274 G>A maps to NM_000477.5 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr4:74285274 G>A maps to NM_000477.5 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr4:74279156 C>T maps to NM_000477.5 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:74274459 G>A maps to NM_000477.5 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr3:105252535 T>A did not map to a codon.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr19:49967903 C>T maps to NM_153329.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:49965029 G>A maps to NM_153329.3 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:49971799 C>T maps to NM_153329.3 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr19:49965834 C>T maps to NM_153329.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:49967511 G>A maps to NM_153329.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr19:49971708 C>T maps to NM_153329.3 D670D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr19:49972188 C>T maps to NM_153329.3 R731R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr10:97373915 C>T maps to NM_002860.3 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:97376260 G>A maps to NM_002860.3 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:75567868 C>T maps to NM_000689.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr9:75540480 C>G maps to NM_000689.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr15:58302943 G>A maps to NM_003888.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr15:58256148 G>A maps to NM_003888.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr15:58285148 G>A maps to NM_003888.2 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr15:101434205 C>T maps to NM_000693.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr9:38396623 C>T maps to NM_000692.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr12:105454803 G>C maps to NM_001034173.3 S365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr12:105440690 C>T maps to NM_001034173.3 K581K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr12:105440729 G>A maps to NM_001034173.3 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr12:105460398 G>A maps to NM_001034173.3 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:112229905 C>G maps to NM_000690.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr17:19648433 C>T maps to NM_000691.4 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr17:19645468 C>T maps to NM_000691.4 E179E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:19642973 G>A maps to NM_000691.4 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:19646658 G>A maps to NM_000691.4 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr17:19576480 G>A maps to NM_001031806.1 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:19576462 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr17:19566757 C>T maps to NM_001031806.1 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr17:19555083 C>T maps to NM_001031806.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:67789326 G>A maps to NM_001161473.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr11:67790063 C>A did not map to a codon.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr11:67433047 C>T maps to NM_001031615.1 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr11:67433662 G>A maps to NM_001031615.1 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr6:24503624 C>G maps to NM_170740.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr6:24503594 C>T maps to NM_170740.1 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:24528377 C>T maps to NM_170740.1 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr6:24520657 G>T maps to NM_170740.1 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr14:74533461 C>T maps to NM_005589.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr5:125903969 C>G maps to NM_001182.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr6:135239741 G>A maps to NM_022568.3 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:135239771 A>G maps to NM_022568.3 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr6:135254132 G>T maps to NM_022568.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:165648805 G>T maps to NM_000696.3 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr1:165638533 G>A maps to NM_000696.3 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr1:165667615 G>T maps to NM_000696.3 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr16:30081175 G>A maps to ENST00000395248 Q329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr16:30080178 G>A maps to ENST00000395248 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr9:104192126 G>A maps to NM_000035.3 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr9:104187277 G>C maps to NM_000035.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr9:104189817 G>A maps to NM_000035.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr17:26901770 T>C maps to NM_005165.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:26902292 G>A maps to NM_005165.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr16:5127976 C>G maps to NM_019109.4 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr12:34179258 C>T maps to NM_032834.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr12:38714393 T>C maps to NM_001013620.3 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr22:50303671 G>A maps to NM_024105.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr22:50304121 G>A maps to NM_024105.3 Y143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr22:50301457 G>C maps to NM_024105.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr22:50307275 G>A maps to NM_024105.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr23:111000831 A>G did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:110970868 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr23:110951457 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr23:111000890 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr3:125650571 G>A maps to NM_001195223.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr3:125651508 A>G maps to NM_001195223.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:101980575 C>T maps to NM_033087.3 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:101980998 C>T maps to NM_033087.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr9:101984088 C>A maps to NM_033087.3 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr9:101981109 G>T maps to NM_033087.3 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr13:37563686 A>G maps to NM_013338.4 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr13:37559763 A>G maps to NM_013338.4 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:77832129 G>A maps to NM_024079.4 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr11:111724208 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr2:29543680 C>T maps to NM_004304.3 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:29519818 G>A maps to NM_004304.3 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr2:29430113 G>T maps to NM_004304.3 G1287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr14:78142081 C>T maps to NM_006020.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr14:78174277 G>T maps to NM_006020.2 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:109526079 G>A maps to NM_001145375.1 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:109530579 G>A maps to NM_001145375.1 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr7:102100146 C>G maps to NM_017621.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr17:18088114 C>T maps to ENST00000261650 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr17:18088105 C>T maps to ENST00000261650 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr19:36501540 G>A maps to ENST00000455847 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr19:6372968 G>A maps to NM_032306.3 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:3730542 C>T maps to ENST00000403787 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr2:73678072 C>A maps to NM_015120.4 S1472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr2:73799943 C>G maps to NM_015120.4 S3646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr2:73682347 G>T maps to NM_015120.4 E2533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr2:73675450 G>A maps to NM_015120.4 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr2:73717127 C>G maps to NM_015120.4 S2680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr2:73800451 G>A maps to NM_015120.4 Q3815Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:73677372 C>G maps to NM_015120.4 S1239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:73677409 C>T maps to NM_015120.4 V1251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr2:73717137 A>G maps to NM_015120.4 V2683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:73717552 G>T maps to NM_015120.4 E2822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr2:73717005 C>T maps to NM_015120.4 F2639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr2:73786207 G>A maps to NM_015120.4 K3440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:73716790 A>T maps to NM_015120.4 K2568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr2:73718394 C>T maps to NM_015120.4 T3102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr2:73678880 C>T maps to NM_015120.4 Q1742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:73718361 G>A maps to NM_015120.4 S3091S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr2:73679002 G>C maps to NM_015120.4 L1782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:6903687 C>T maps to NM_000697.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr17:7976525 C>T maps to NM_001139.2 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr17:7976112 C>G maps to NM_001139.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr17:4536453 C>A maps to NM_001140.3 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr17:7948952 C>G maps to NM_001141.2 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:45907637 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:45877974 C>T maps to NM_000698.2 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr2:233321092 G>A maps to NM_001631.3 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:233321155 C>T maps to NM_001631.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:233322745 C>T maps to NM_001631.3 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr2:233322987 C>G maps to NM_001631.3 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:233321359 G>A maps to NM_001631.3 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr4:113353309 C>T maps to NM_025144.3 H869H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr4:113353516 C>T maps to NM_025144.3 S938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr4:113351677 G>A maps to NM_025144.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr18:56246896 G>A maps to NM_052947.3 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr18:56171379 C>T maps to NM_052947.3 E2010E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:85407672 G>A maps to NM_020778.4 E1702E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr15:85401088 C>T maps to NM_020778.4 L1242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr15:85401043 G>A maps to NM_020778.4 Q1227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr15:85401421 C>T maps to NM_020778.4 L1353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr15:85383291 C>G maps to NM_020778.4 S463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr15:85383865 C>T maps to NM_020778.4 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr15:85400402 C>T maps to NM_020778.4 Q1014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr2:233245161 C>G maps to NM_001632.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:233243988 G>A maps to NM_001632.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr2:233245450 C>T maps to NM_001632.3 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr2:233274449 C>G maps to NM_031313.2 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr2:202580522 C>T maps to NM_020919.3 K1292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:202625888 G>C maps to NM_020919.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:202593267 G>A maps to NM_020919.3 F936F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr3:46713516 C>T maps to NM_147129.3 T847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:46712989 G>A maps to NM_147129.3 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr3:46716126 G>A maps to NM_147129.3 F786F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr2:202400896 C>T maps to NM_001168221.1 Q451Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr2:203836413 A>G maps to NM_024744.14 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:203826042 G>A maps to NM_024744.14 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:203842023 C>G maps to NM_024744.14 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr2:203817340 G>A maps to NM_024744.14 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:203847102 G>C maps to NM_024744.14 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:203820395 G>T did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr12:85680719 T>C maps to NM_006982.2 Y207Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:85677572 C>A maps to NM_006982.2 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr11:44296954 G>A maps to NM_021926.3 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr17:33520603 C>A maps to NM_152462.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr17:33521266 G>A maps to NM_152462.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr17:33520471 G>C maps to NM_152462.2 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr17:33521025 G>A maps to NM_152462.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr17:7385833 C>G maps to NM_001102614.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr5:34004717 G>A maps to NM_001167595.1 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:33997420 G>A maps to NM_001167597.1 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr5:33997531 C>G maps to NM_001167596.1 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr5:33989415 C>A maps to NM_001167595.1 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr5:34005930 C>T maps to NM_001167595.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr5:34008100 G>A maps to NM_001167595.1 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:71459066 C>T maps to NM_016519.4 D13D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr9:116840417 C>T maps to NM_001633.3 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr9:116840477 G>A maps to NM_001633.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:46563760 G>A maps to ENST00000458649 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:46567155 G>C maps to ENST00000458649 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:46567256 G>A maps to ENST00000458649 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:46418999 C>T maps to ENST00000458649 *1299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr11:46419134 G>C maps to ENST00000458649 V1254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr11:46569364 A>T did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr11:46563835 G>A maps to ENST00000458649 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:46568821 C>T maps to ENST00000458649 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:111213514 C>T maps to NM_001634.4 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr12:96354208 C>T maps to NM_152435.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:96360279 C>A maps to NM_152435.2 S396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr12:96361532 G>A did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:2570862 G>A maps to NM_001145815.1 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr16:2570886 C>T maps to NM_001145815.1 F67F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BT-A3PH-01A-11D-A21Z-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:2580758 G>A maps to NM_001048212.3 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr16:2571042 C>G maps to NM_001145815.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:2577862 C>T maps to NM_001145815.1 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:11316857 T>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr24:6736206 T>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr16:56397993 G>C maps to NM_001144.4 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr16:56436916 C>T maps to NM_001144.4 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr16:56423189 G>A maps to NM_001144.4 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr16:56443413 C>T maps to NM_001144.4 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr19:2251758 C>T maps to NM_000479.3 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:53825227 C>T maps to NM_020547.2 Q565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr12:53824974 G>A maps to NM_020547.2 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr12:53819269 A>G maps to NM_020547.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr12:53819353 C>T maps to NM_020547.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:110051489 C>T maps to NM_020703.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:110050082 C>T maps to NM_020703.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr1:110050373 G>A maps to NM_020703.2 V387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr1:110050079 G>A maps to NM_020703.2 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr12:47472707 C>T maps to NM_001143668.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:47472632 G>T maps to NM_001143668.1 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:47472632 G>A maps to NM_001143668.1 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr12:47472392 C>T maps to NM_001143668.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr3:49756010 C>T maps to NM_198722.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr3:49756493 C>T maps to NM_198722.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr3:49756386 G>T maps to NM_198722.2 S171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr3:49756391 G>A maps to NM_198722.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr3:49755908 C>T maps to NM_198722.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:49755779 A>G maps to NM_198722.2 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:49756421 G>C maps to NM_198722.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr3:49756685 G>A maps to NM_198722.2 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr23:109561180 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr23:109561232 C>T did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:109459791 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr23:109445720 C>G did not map to a codon.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr2:128628926 G>C maps to NM_031445.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr14:103390063 C>T maps to NM_030943.3 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr14:103390132 C>A maps to NM_030943.3 C43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:31842007 G>A maps to NM_001113402.1 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr12:31850793 G>C maps to NM_001113402.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr23:112033958 G>C did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr23:112033994 G>A did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:112033887 C>T did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:112025816 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr23:112058801 T>G did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:112054508 C>T did not map to a codon.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr23:112058692 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:112048227 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr23:112022305 C>T did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:94554951 C>T maps to NM_130847.2 Q460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr11:94599319 G>A maps to NM_130847.2 W825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:94533393 C>G maps to NM_130847.2 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:94533412 C>T maps to NM_130847.2 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:94597965 C>T maps to NM_130847.2 I734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:115220578 C>T maps to NM_000036.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:115236062 C>A maps to NM_000036.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr1:110170871 G>A maps to ENST00000393689 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr1:110172958 G>A maps to ENST00000393689 P750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr1:110172444 G>T maps to ENST00000393689 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:110169424 G>C maps to ENST00000393689 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:10483089 G>A maps to NM_000480.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr11:10518418 C>T maps to NM_000480.2 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr7:38424442 C>T maps to NM_001635.3 E688E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:38431489 G>A maps to NM_001635.3 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr7:38500983 G>A maps to NM_001635.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr3:49459596 A>T maps to NM_000481.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr4:71396886 C>A maps to NM_212557.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr1:104297225 T>A maps to NM_001008218.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:104114772 C>T maps to ENST00000305865 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:104118136 G>A maps to NM_020978.3 W359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr2:112608430 T>C maps to NM_022662.2 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:112588951 G>A maps to NM_022662.2 Q846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:112589008 G>A maps to NM_022662.2 Q827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr2:112608430 T>G maps to NM_022662.2 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:112614423 G>A maps to NM_022662.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr2:112605343 G>T maps to NM_022662.2 Y583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr10:73992846 G>T maps to NM_173473.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:140075250 G>A maps to NM_013366.3 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:140082486 C>A maps to NM_013366.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:25419343 C>T maps to ENST00000510092 R729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr4:25391769 C>T maps to ENST00000510092 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:121783660 C>A maps to NM_016237.4 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr12:121779867 C>A maps to NM_016237.4 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr12:110819629 G>A maps to NM_016238.2 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr12:110832920 T>C maps to NM_016238.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr14:77275516 T>C maps to NM_015305.3 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr14:77273073 G>T maps to NM_015305.3 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr14:77255660 G>C maps to NM_015305.3 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr14:77273019 G>A maps to NM_015305.3 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr14:77256981 A>G maps to NM_015305.3 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:6378703 G>C maps to NM_001147.2 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr8:6360673 G>T maps to NM_001147.2 S480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr8:6389912 C>T maps to NM_001147.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:854973 G>C maps to NM_015985.2 S435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr20:865892 C>T maps to NM_015985.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr1:178820443 G>A maps to NM_004673.3 C432C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:129870632 C>T maps to NM_012098.2 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr9:129870395 C>T maps to NM_012098.2 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr9:129870587 G>C maps to NM_012098.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr19:8438673 G>A maps to NM_139314.1 K375K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr19:8436323 C>G maps to NM_139314.1 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr19:8429402 G>C maps to NM_139314.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr19:8431136 C>T maps to NM_139314.1 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr19:10206747 G>A maps to NM_031917.2 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:11249683 C>T maps to NM_021146.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr1:11249968 C>T maps to NM_021146.2 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr8:41583407 C>A maps to ENST00000415018 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr8:41552279 G>A maps to ENST00000415018 R1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr8:41526083 T>C did not map to a codon.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr8:41526054 C>T maps to ENST00000415018 S1708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr8:41556983 C>T maps to ENST00000415018 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr8:41572562 G>T maps to ENST00000415018 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr8:41547810 C>T maps to ENST00000415018 A1346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr8:41553999 G>A maps to ENST00000415018 T947T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr4:114170942 T>A maps to NM_001148.4 C305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr4:114251494 T>C maps to NM_001148.4 C998C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:114275389 G>A maps to NM_001148.4 S1872S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:114276928 T>G maps to NM_001148.4 P2385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:114279628 C>T maps to NM_001148.4 I3285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr4:114294583 G>A maps to NM_001148.4 K3946K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr4:114158180 A>G maps to NM_001148.4 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr4:114275327 G>T maps to NM_001148.4 E1852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr4:114276667 G>A maps to NM_001148.4 E2298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr4:114179249 C>A maps to NM_001148.4 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr4:114286204 C>T maps to NM_001148.4 L3633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr4:114284602 G>A maps to NM_001148.4 E3622E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr4:114280166 G>T maps to NM_001148.4 E3465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr4:114275803 C>G maps to NM_001148.4 L2010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr4:114286339 T>G did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr4:114294532 C>T maps to NM_001148.4 N3929N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr4:114257929 C>T maps to NM_001148.4 S1263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr4:114232531 C>T maps to NM_001148.4 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:114177075 C>T maps to NM_001148.4 N392N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr4:114278500 C>A maps to NM_001148.4 P2909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr10:61865720 C>T maps to NM_020987.2 E1090E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr10:61822995 C>T maps to NM_020987.2 S4156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr10:61965627 A>G maps to NM_020987.2 H405H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr10:61829046 T>C maps to NM_020987.2 K3864K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr10:61830480 C>T maps to NM_020987.2 G3386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:61847918 G>A maps to NM_020987.2 R1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr10:61828485 C>T maps to NM_020987.2 T4051T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr10:62039328 T>A maps to NM_020987.2 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr10:61965584 G>A maps to NM_020987.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr10:61835133 T>A maps to NM_020987.2 A1835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr10:61926584 C>A maps to NM_020987.2 E850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr10:61830969 C>T maps to NM_020987.2 V3223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:190603289 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr2:190585419 C>A maps to NM_144708.3 R848R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr2:190611322 G>A maps to NM_144708.3 Q1425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr15:65208071 G>A maps to NM_182703.3 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr15:65208099 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr15:65226397 C>T maps to NM_182703.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:54554976 C>A maps to NM_153228.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr17:54428175 C>T maps to NM_153228.2 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr17:54526503 G>A maps to NM_153228.2 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr17:54526476 G>A maps to NM_153228.2 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr17:54559799 C>T maps to NM_153228.2 D728D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr17:4080442 G>C maps to NM_016376.3 S919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:4086694 G>A maps to NM_016376.3 V650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr17:4074068 G>A maps to NM_016376.3 Q1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr17:4111257 G>A maps to NM_016376.3 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr17:4080557 G>A maps to NM_016376.3 Q881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:4111337 G>A maps to NM_016376.3 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr5:14746023 G>A maps to NM_054027.4 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr5:139876175 C>T maps to ENST00000253810 Q773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr5:139917004 A>G maps to ENST00000253810 P2370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr5:139914967 C>G maps to ENST00000253810 S2291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr5:139781719 C>T maps to ENST00000253810 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr5:139892430 C>T maps to ENST00000253810 Q1375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr5:139908298 C>G maps to ENST00000253810 S1923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr5:139917810 C>T maps to ENST00000253810 Q2474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr5:139885447 T>C maps to ENST00000253810 R1134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr5:139908518 C>T maps to ENST00000253810 S1996S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr5:139903724 A>G maps to ENST00000253810 K1464K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr5:139906653 A>G maps to ENST00000253810 V1694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr7:91981820 G>A maps to NM_019004.1 W421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr7:91957102 G>T maps to NM_019004.1 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr7:91936754 C>T maps to NM_019004.1 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr7:91981896 C>G maps to NM_019004.1 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr12:133327435 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:133327435 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr12:133306380 C>T maps to NM_015114.1 R789R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr12:133306395 C>T maps to NM_015114.1 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr12:133313490 C>T maps to NM_015114.1 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr12:133306728 C>T maps to NM_015114.1 R673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr12:133331375 G>T maps to NM_015114.1 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr2:241439946 C>A maps to ENST00000401804 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:241468764 G>T maps to ENST00000401804 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:241420352 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr2:241463378 C>T maps to ENST00000401804 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr2:241421609 C>A maps to ENST00000401804 E959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:241465164 G>A maps to ENST00000401804 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr5:72858587 G>T maps to NM_023039.4 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr16:89350708 C>T maps to NM_013275.4 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr16:89348311 C>T maps to NM_013275.4 V1546V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr16:89348355 C>A maps to NM_013275.4 E1532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:89346346 T>C maps to NM_013275.4 A2201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr16:89351470 C>T maps to NM_013275.4 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr16:89350176 C>A maps to NM_013275.4 E925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:89346321 C>A maps to NM_013275.4 E2210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:89349018 G>A maps to NM_013275.4 R1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:89350612 C>T maps to NM_013275.4 K779K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr16:89357081 G>A maps to NM_013275.4 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr16:89351726 G>C maps to NM_013275.4 S408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr16:89347240 G>A maps to NM_013275.4 L1903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr16:89350972 G>A maps to NM_013275.4 Y659Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr16:89347298 G>C maps to NM_013275.4 S1884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr16:89347324 G>A maps to NM_013275.4 V1875V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr16:89347744 G>A maps to NM_013275.4 L1735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr16:89348907 C>A maps to NM_013275.4 E1348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:89352492 G>A maps to NM_013275.4 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr16:89337257 G>C maps to NM_013275.4 L2591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr16:89350675 C>T maps to NM_013275.4 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr16:89350021 C>T maps to NM_013275.4 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr18:9258745 A>G maps to NM_015208.3 P1827P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr18:9256686 C>G maps to NM_015208.3 S1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr18:9258380 G>T maps to NM_015208.3 E1706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr18:9256538 G>T maps to NM_015208.3 E1092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr18:9258644 C>T maps to NM_015208.3 Q1794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr18:9257771 G>T maps to NM_015208.3 E1503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr18:9256977 C>G maps to NM_015208.3 S1238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr18:9254671 A>G maps to NM_015208.3 K469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr18:9254967 C>A maps to NM_015208.3 S568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr18:9256861 C>G maps to NM_015208.3 L1199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr18:9255421 A>G maps to NM_015208.3 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:110463572 G>A maps to NM_033121.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr17:27935028 G>A maps to NM_152345.4 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:70790602 G>C maps to NM_030816.4 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:70736617 T>C maps to NM_030816.4 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:70819989 G>A maps to NM_030816.4 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr11:67059206 C>T maps to NM_207354.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr11:67068496 G>A maps to NM_207354.2 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr4:73957395 T>A maps to NM_032217.3 T1983T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:73981624 C>T maps to NM_032217.3 V1399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:73990761 G>C maps to NM_032217.3 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr4:73957548 C>T maps to NM_032217.3 L1932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr4:73944482 C>T maps to NM_032217.3 G2428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr4:74013059 G>A maps to NM_032217.3 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr4:74008084 C>T maps to NM_032217.3 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr9:69423626 T>C maps to NM_001098805.1 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr2:97505286 C>T maps to NM_144994.7 *306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr19:4216827 C>T maps to ENST00000262970 N647N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr19:4207840 C>T maps to ENST00000262970 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:27294519 C>G maps to NM_014915.2 *1711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr10:27350130 G>A maps to NM_014915.2 N468N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr10:27294536 C>T maps to NM_014915.2 K1705K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr10:27324213 T>A maps to NM_014915.2 L1055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:33135287 G>A maps to NM_032139.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr19:33135366 G>C maps to NM_032139.2 S130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:33110219 G>A maps to NM_032139.2 F651F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr3:15711998 C>T maps to NM_015199.3 L980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:15731547 C>T maps to NM_015199.3 K617K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr10:37486373 C>A maps to ENST00000374660 A957A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr10:37454020 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr10:37447344 G>C maps to ENST00000374660 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr18:14752672 G>A maps to NM_001145029.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr18:14850273 A>T maps to NM_001145029.1 R1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr18:14852239 C>T maps to NM_001145029.1 R1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr18:14764039 T>C maps to NM_001145029.1 N392N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr18:14843084 A>T maps to NM_001145029.1 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr12:52282068 G>A maps to NM_182608.3 W33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:145474161 G>T maps to NM_001039888.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr1:145474701 G>A maps to NM_001039888.2 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr5:79855445 T>C maps to NM_001004441.2 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr5:79855574 C>G maps to NM_001004441.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:145562891 T>G maps to NM_144698.3 Y860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:145567754 G>A maps to NM_144698.3 *1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr1:145562607 G>T maps to NM_144698.3 E766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:145561388 C>T maps to NM_144698.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:145561859 G>A maps to NM_144698.3 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:145561531 C>G maps to NM_144698.3 S407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:97779538 C>T maps to NM_001164315.1 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:97849203 C>T maps to NM_001164315.1 Q616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:98206121 G>A maps to NM_025190.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr4:186318344 C>T maps to NM_181726.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr17:48777204 C>A maps to NM_052855.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr5:132150605 G>A maps to NM_175873.4 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr5:132149837 G>A maps to NM_175873.4 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr2:197987388 C>T maps to NM_001195144.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:197986229 G>A maps to NM_001195144.1 H244H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr2:197889931 T>A maps to NM_001195144.1 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr11:94231643 T>C maps to NM_017704.2 Y222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr11:94231250 G>C maps to NM_017704.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr20:10030757 C>A maps to NM_198798.1 S514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr20:10036256 G>A maps to NM_198798.1 Q760Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr20:10030150 A>T maps to NM_198798.1 K312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr4:125591959 T>C maps to NM_020337.2 Q824Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr4:125600038 C>T maps to NM_020337.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:56637605 C>T maps to NM_173595.3 L981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr2:71206451 G>A maps to NM_001115116.1 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr22:38228751 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:55407500 C>T maps to NM_024669.2 Q358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr5:55396108 C>T maps to NM_024669.2 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr4:77818849 G>A maps to NM_001029870.1 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:77818387 C>T maps to NM_001029870.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr4:77817829 G>T maps to NM_001029870.1 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr4:77816857 G>A maps to NM_001029870.1 T715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:77816953 C>T maps to NM_001029870.1 Q683Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:110373334 C>T maps to NM_023016.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr2:110373433 A>G maps to NM_023016.3 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:118893526 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr23:118893486 C>T did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:118893472 G>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr6:90305672 C>G maps to ENST00000339746 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:34985274 G>C maps to NM_015245.2 R483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:35047441 C>T maps to NM_015245.2 V811V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr6:34985576 T>A maps to NM_015245.2 L584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:34985688 C>T maps to NM_015245.2 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:35051237 C>T maps to NM_015245.2 S984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:99640172 G>C maps to NM_152788.3 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:99201645 G>A maps to NM_181670.2 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:99640603 C>A maps to NM_152788.3 E599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr12:99192765 C>G maps to NM_152788.3 L1071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:100378000 C>T maps to NM_152788.3 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:100205989 C>T maps to NM_152788.3 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:100048913 T>A maps to NM_152788.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr12:99447087 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr12:99837570 T>A maps to NM_152788.3 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:99139546 A>G maps to NM_181670.2 I501I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr12:100377963 G>A maps to NM_152788.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr16:4749141 C>G maps to NM_133450.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr16:4764076 C>G maps to NM_133450.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:4755174 G>A maps to NM_133450.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr16:21261823 G>T maps to NM_145865.2 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr16:21261961 G>T maps to NM_145865.2 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:101552767 C>T maps to ENST00000375018 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr9:101536317 C>T maps to ENST00000375018 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr9:101540607 G>A maps to ENST00000375018 D489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr2:220097402 C>T maps to NM_001042410.1 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr7:36459776 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:36438904 G>A maps to NM_018685.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr11:70028636 C>T maps to NM_018043.5 F811F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr11:69954463 T>C maps to NM_018043.5 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr11:70011652 C>T maps to NM_018043.5 N676N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:70003069 G>A maps to NM_018043.5 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr11:69962592 C>T maps to NM_018043.5 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:69924768 C>A maps to NM_018043.5 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr11:70007394 C>A maps to NM_018043.5 V569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr11:70007295 C>T maps to NM_018043.5 G536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr11:70028708 C>G maps to NM_018043.5 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr3:43618535 G>T maps to NM_018075.3 Y270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:5853335 G>A maps to ENST00000356134 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr11:26463549 C>T maps to NM_031418.2 Y44Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr11:26556100 C>G maps to NM_031418.2 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:101490419 C>T maps to ENST00000392977 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:101493395 G>T maps to ENST00000392977 E683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr12:101480520 G>A maps to ENST00000392977 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr12:101493478 C>T maps to ENST00000392977 F710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr12:101442179 G>A did not map to a codon.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr12:101433737 T>C maps to ENST00000392977 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr11:22249086 C>T maps to NM_213599.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr11:22242654 C>T maps to NM_213599.2 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr12:45810575 C>T maps to NM_001142679.1 D702D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr12:45781980 A>C maps to NM_001142679.1 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr2:242148968 C>T maps to NM_001001891.3 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:242135137 G>T maps to NM_001001891.3 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:242163166 C>T maps to NM_001001891.3 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:242157736 C>T maps to NM_001001891.3 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr2:242157299 C>T maps to NM_001001891.3 I778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:242128094 G>A maps to NM_001001891.3 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr2:242149759 C>A maps to NM_001001891.3 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr2:242147075 C>T maps to NM_001001891.3 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:17440961 C>T maps to NM_020959.2 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:17440785 G>A maps to NM_020959.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr19:17442155 C>T maps to NM_020959.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr19:17441039 C>T maps to NM_020959.2 K389K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:433381 G>A maps to NM_001012302.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr11:428561 G>A maps to NM_001012302.2 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:69080225 C>T maps to NM_006305.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:69079814 C>T maps to NM_006305.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr15:69076811 C>T maps to NM_006305.3 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr15:69080183 T>C maps to NM_006305.3 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr12:48866716 C>T maps to NM_012404.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:150193048 G>A maps to NM_030920.3 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr15:90348335 C>T maps to NM_001150.2 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr15:90348603 G>A maps to NM_001150.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr15:90333726 C>G maps to NM_001150.2 V905V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr2:69408958 G>A maps to NM_032208.2 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:80976546 C>T maps to NM_001145794.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:80976621 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:46135370 C>A maps to NM_001128324.1 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr10:46135390 G>C maps to NM_001128324.1 S197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:75775775 G>T maps to NM_000700.1 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr4:169108569 T>C maps to NM_007193.3 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr4:169105799 C>T maps to NM_007193.3 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr10:81932587 T>C maps to NM_145869.1 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:124693584 C>T maps to NM_001003954.1 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WY-01A-11D-A22Z-08 chr8:124693556 G>A maps to NM_001003954.1 Q333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr8:124748036 G>A maps to NM_001003954.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr8:124696897 C>T maps to NM_001003954.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr8:124714887 G>A maps to NM_001003954.1 Y101Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr8:124710769 C>T maps to NM_001003954.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr8:124710781 G>C maps to NM_001003954.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr15:60648135 C>T maps to NM_001002858.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr2:70015205 C>T maps to NM_001153.3 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr4:122590870 C>T maps to NM_001154.3 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr5:150512103 C>T maps to NM_001155.4 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr10:75135975 C>G did not map to a codon.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr10:75135975 C>G did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:75135897 C>T maps to NM_004034.2 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr10:75138734 G>T maps to NM_004034.2 Y426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:150960574 C>T maps to NM_003568.2 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr1:150967159 C>T maps to NM_003568.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:150967796 G>T maps to NM_003568.2 *346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:150960607 G>T maps to NM_003568.2 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr7:36571797 G>A maps to NM_001177506.1 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr7:36677471 C>T maps to NM_001177506.1 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr7:36662828 T>C maps to NM_001177506.1 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr17:40997325 C>G maps to NM_009590.2 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr17:40996882 G>T maps to NM_009590.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr17:41003698 G>A maps to NM_003734.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr2:201462143 G>A maps to NM_001159.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr2:201503026 T>A did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:201468753 C>T maps to NM_001159.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr2:201477418 G>T maps to NM_001159.3 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr2:201533503 C>G maps to NM_001159.3 S1259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:201469495 G>T maps to NM_001159.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:201533366 A>G maps to NM_001159.3 G1213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr22:29737620 G>A maps to NM_001127.3 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr22:29730358 G>C maps to NM_001127.3 S735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:29752416 C>T maps to NM_001127.3 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:29737584 G>A maps to NM_001127.3 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:29735104 G>A maps to NM_001127.3 F679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:29738336 G>T maps to NM_001127.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr22:29755926 G>C maps to NM_001127.3 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr22:29738342 C>T maps to NM_001127.3 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr22:29745233 G>A maps to NM_001127.3 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr22:29734997 G>T maps to NM_001127.3 S715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:71805128 G>A maps to ENST00000423132 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr16:71792811 C>T maps to ENST00000423132 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr16:71807213 G>A maps to ENST00000423132 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr16:71807213 G>T maps to ENST00000423132 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr14:24029008 C>T maps to NM_003917.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr14:24029580 C>A maps to NM_003917.2 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:16337278 C>T maps to NM_001130524.1 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:10692041 C>T maps to ENST00000453102 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr19:10689594 G>C maps to ENST00000453102 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr19:10687927 G>A maps to ENST00000453102 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:10692455 G>A maps to ENST00000453102 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr19:10692043 G>A maps to ENST00000453102 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:10692497 G>C maps to ENST00000453102 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr19:10692494 G>A maps to ENST00000453102 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr7:100802371 G>A maps to NM_001283.3 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr23:15864094 C>T did not map to a codon.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr23:15870490 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr11:984715 C>T maps to ENST00000332231 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr11:1009193 C>T maps to ENST00000332231 Q840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr17:33984671 G>A maps to NM_001030006.1 Q617Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr3:183901307 G>A maps to ENST00000411763 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr19:47349396 G>A maps to NM_004069.3 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:47349273 G>A maps to NM_004069.3 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr19:47349384 G>T maps to NM_004069.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:77406124 G>C maps to NM_003664.3 S768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:77521395 T>C maps to NM_003664.3 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr15:83346883 G>A maps to NM_004644.3 N406N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:83335619 G>A maps to NM_004644.3 D577D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:83346519 T>G maps to NM_004644.3 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr15:83357942 C>T maps to NM_004644.3 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr15:83331640 C>A maps to NM_004644.3 E861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:2116612 C>T maps to ENST00000355272 E664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:2130434 C>T maps to ENST00000355272 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr19:2132478 G>A maps to ENST00000355272 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:2110176 G>T maps to ENST00000355272 V1074V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr10:75898116 G>T maps to NM_207012.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:42024873 C>T maps to NM_006803.3 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr8:42019805 G>A maps to NM_006803.3 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr15:90378797 G>A maps to ENST00000398333 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr15:90432324 G>A maps to ENST00000398333 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr1:114440494 C>T maps to NM_006594.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr15:51250829 C>T maps to NM_007347.3 Q564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr15:51250931 G>T maps to NM_007347.3 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr7:99704426 C>T maps to ENST00000429084 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr14:31535512 G>A maps to NM_007077.3 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr12:99042265 A>G maps to NM_181861.1 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr12:99076994 C>T maps to NM_181861.1 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:99053032 C>T maps to NM_181861.1 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr12:99076979 C>T maps to NM_181861.1 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr9:72047529 G>A maps to NM_001163.3 I788I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr9:72064580 C>G maps to NM_001163.3 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr9:72072052 A>G maps to NM_001163.3 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr15:29393869 G>A maps to NM_005503.3 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:29367149 G>A maps to NM_005503.3 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr15:29346935 G>A maps to NM_005503.3 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr15:29400576 C>T maps to NM_005503.3 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr15:29346683 G>A maps to NM_005503.3 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr15:29346110 C>T maps to NM_005503.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:29346317 G>C maps to NM_005503.3 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr15:29346704 C>T maps to NM_005503.3 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:6424558 G>A maps to ENST00000389906 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr10:26800719 G>A maps to NM_019043.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr10:26830539 G>A maps to NM_019043.3 Q358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr10:26830575 T>C maps to NM_019043.3 H370H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr4:41015819 A>G maps to NM_004307.1 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:139938223 G>C maps to ENST00000354402 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr5:139941015 C>A maps to ENST00000354402 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr5:139939924 G>A maps to ENST00000354402 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:112154980 G>T maps to NM_001127510.2 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr5:112174587 T>G maps to NM_001127510.2 V1099V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:112174756 G>T maps to NM_001127510.2 E1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:112178931 G>A maps to NM_001127510.2 W2547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:112178775 A>G maps to NM_001127510.2 T2495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr5:112174551 C>G maps to NM_001127510.2 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr5:112103070 G>T maps to NM_001127510.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr5:112174240 G>T maps to NM_001127510.2 E984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr5:112177900 C>T maps to NM_001127510.2 R2204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr5:112179675 A>G maps to NM_001127510.2 A2795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr5:112174501 C>T maps to NM_001127510.2 Q1071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr5:112175014 C>T maps to NM_001127510.2 Q1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr19:1453083 G>A maps to NM_005883.2 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:1453565 G>A maps to NM_005883.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:1461972 G>A maps to NM_005883.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:1462068 G>T maps to NM_005883.2 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:1462113 C>T maps to NM_005883.2 I597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr19:1455192 C>G maps to NM_005883.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:1455390 G>A maps to NM_005883.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr18:10468574 C>T maps to ENST00000423585 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr18:10485672 C>A maps to ENST00000423585 S381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr1:159557900 G>C maps to NM_001639.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr1:159558020 C>T maps to NM_001639.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:49716345 G>A maps to ENST00000438011 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr3:49716300 C>T maps to ENST00000438011 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr3:49720139 C>T maps to ENST00000438011 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr3:49713346 C>G maps to ENST00000438011 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:55028738 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr23:55033262 G>A did not map to a codon.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr23:55033805 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:55033585 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr23:55033378 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr1:150238947 G>A maps to NM_001077628.1 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:150240427 G>A maps to NM_001077628.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr15:63594547 C>T maps to NM_031301.3 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr11:43333682 G>A maps to NM_001142930.1 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr1:10511483 C>G maps to NM_198544.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr2:68753370 C>T maps to NM_173545.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr2:68729888 G>A maps to NM_173545.2 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:57003560 G>A maps to NM_005161.4 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr11:57004121 G>A maps to NM_005161.4 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr19:36369851 C>T maps to NM_001024807.1 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:36365500 C>T maps to NM_001024807.1 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr19:36370100 C>A maps to NM_001024807.1 I613I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr19:36369486 G>A maps to NM_001024807.1 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr19:36362810 G>A maps to NM_001024807.1 E241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:36368636 G>T maps to NM_001024807.1 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr11:130005575 C>T maps to NM_001642.2 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr11:129992403 C>T maps to NM_001642.2 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr11:116707811 C>T maps to NM_000039.1 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:156563827 G>A maps to ENST00000446584 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:156562242 C>T maps to ENST00000446584 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:156561601 C>T maps to ENST00000446584 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr1:156561718 G>A maps to ENST00000446584 L59L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-4Z-AA86-01A-11D-A391-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-4Z-AA86-01A-11D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr1:161192272 C>T maps to ENST00000443363 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr1:161192748 C>G maps to NM_001643.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr11:116692359 G>T maps to NM_000482.3 Y138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr11:116691981 C>T maps to NM_000482.3 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr11:116692017 G>C maps to NM_000482.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:116691986 G>A maps to NM_000482.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:21233208 A>G maps to NM_000384.2 Y2177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:21233217 C>T maps to NM_000384.2 L2174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr2:21238037 A>T maps to NM_000384.2 P1201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr2:21235227 A>G maps to NM_000384.2 S1504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr2:21228216 A>G maps to NM_000384.2 N3841N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:21225672 T>C maps to NM_000384.2 K4207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr2:21233835 G>A maps to NM_000384.2 V1968V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr2:21242617 G>A maps to NM_000384.2 Y992Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr2:21234810 C>A maps to NM_000384.2 A1643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr2:21239516 C>T maps to NM_000384.2 A1042A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr2:21235181 G>A maps to NM_000384.2 L1520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:21238403 C>A maps to NM_000384.2 E1116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:21246546 C>T maps to NM_000384.2 R818R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:21247963 C>T maps to NM_000384.2 E759E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:21229815 A>G maps to NM_000384.2 H3308H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr6:41021205 G>A maps to NM_006789.3 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr22:39355615 G>A maps to NM_001193289.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:39387536 C>T maps to ENST00000402182 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr22:39380187 G>A maps to ENST00000402182 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:39425373 G>A maps to NM_152426.3 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr22:39428282 C>T maps to NM_152426.3 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr22:39425463 C>T maps to NM_152426.3 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr22:39441046 A>C maps to NM_145298.5 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:39477086 C>T maps to NM_021822.3 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:39483103 G>T maps to NM_021822.3 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr22:39497956 C>T maps to NM_001166003.1 H151H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr19:45419474 C>T maps to NM_001645.3 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr19:45451744 C>T maps to NM_000483.3 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr11:116701558 C>T maps to ENST00000360377 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr17:64222144 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr17:64225467 C>T maps to NM_000042.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr22:36661302 C>T maps to NM_145343.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr22:36662036 C>T maps to NM_145343.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr22:36624295 C>G maps to ENST00000451256 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:36623579 G>C maps to ENST00000451256 S407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:36623760 G>A maps to ENST00000451256 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:36624082 A>T maps to ENST00000451256 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr22:36627449 G>A maps to ENST00000451256 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr22:36537276 G>A maps to NM_145640.2 Q394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:36587671 C>T maps to ENST00000332987 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr22:36587752 G>A maps to ENST00000332987 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:36122284 G>A maps to NM_030642.1 W57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:36122300 G>A maps to NM_030642.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:36122894 G>A maps to NM_030642.1 K260K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr22:36122360 G>A maps to NM_030642.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr22:36054799 C>T maps to NM_030641.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr22:36055537 G>A maps to NM_030641.3 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr22:36054950 C>T maps to NM_030641.3 Q114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr6:31625064 C>G maps to NM_019101.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:23898966 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:23897035 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:84310861 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:27284161 C>T maps to NM_000484.3 T600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr21:27264075 C>A maps to NM_000484.3 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr21:27423509 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr21:27269974 C>T maps to NM_000484.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr17:58539172 G>A maps to NM_006380.2 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:58524942 C>T maps to NM_006380.2 *586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:105601807 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:105600931 G>C maps to NM_018171.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr16:88877970 G>A maps to NM_000485.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr9:32986022 G>A maps to NM_001195248.1 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr9:33001575 G>A maps to NM_001195248.1 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:30963147 C>G maps to ENST00000509504 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr7:30951861 C>G maps to ENST00000509504 S290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:154296213 C>T maps to NM_080429.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr1:154296927 C>G maps to NM_080429.2 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:77301510 C>T maps to NM_173039.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr11:77301564 C>G maps to NM_173039.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr11:77301162 G>T maps to NM_173039.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr11:77301495 C>T maps to NM_173039.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr12:50344870 C>T maps to NM_000486.5 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:50355832 C>T maps to NM_001651.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr12:50368530 C>T maps to NM_001652.3 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr9:33395101 C>A maps to NM_001170.1 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:25232863 C>G maps to NM_001169.2 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr5:115298697 T>G maps to NM_173800.4 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr5:115298619 C>T maps to NM_173800.4 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:35230974 C>T maps to NM_014691.2 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr15:35149046 C>T maps to NM_014691.2 P1468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr23:66765005 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:66765707 T>C did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:66765169 A>T did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:66931402 A>T did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:66905852 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr23:66765864 T>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:66941719 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr23:47422402 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr23:47426131 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:47424487 T>C did not map to a codon.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:72418280 C>T maps to NM_001040118.2 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr4:36149305 G>A maps to NM_015230.2 L1021L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr4:36230839 G>T maps to NM_015230.2 S90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr4:36130167 C>T maps to NM_015230.2 W1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr4:36212231 G>A maps to NM_015230.2 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:36212142 C>G maps to NM_015230.2 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr4:36081867 C>T maps to NM_015230.2 T1526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr4:36122815 A>G maps to NM_015230.2 Y1293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr5:141033812 G>A maps to NM_022481.5 Q1447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr5:141053203 G>A maps to NM_022481.5 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:141044641 G>A maps to NM_022481.5 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr5:141059561 G>A maps to NM_022481.5 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr5:141050913 G>C maps to NM_022481.5 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr5:141050833 G>C maps to NM_022481.5 S663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr8:143695044 C>T maps to NM_015193.3 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr11:118452115 T>C maps to ENST00000359415 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:228285295 G>A maps to NM_001024228.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:49334842 C>T maps to NM_001659.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr12:49334729 C>G did not map to a codon.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr12:49332744 G>A maps to NM_001659.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr3:57561322 G>T maps to NM_001660.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr7:127231015 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:127229638 G>A maps to NM_001662.3 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:50360570 G>A maps to NM_001663.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr14:50360894 G>A maps to NM_001663.3 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr20:61919071 C>T maps to NM_175609.1 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:43230282 C>A maps to NM_014570.4 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr8:68150713 G>A maps to NM_006421.3 I1051I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr8:68112662 G>A maps to NM_006421.3 L1785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr8:68150722 C>T maps to NM_006421.3 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr8:68139686 C>T maps to NM_006421.3 R1246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr8:68145141 G>A maps to NM_006421.3 Q1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr8:68130101 G>A maps to NM_006421.3 L1510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr20:47587827 C>T maps to NM_006420.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr20:47588902 C>A maps to NM_006420.2 S489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr20:47615020 G>C maps to NM_006420.2 V1137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr20:47602072 C>T maps to NM_006420.2 F733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr20:47592658 G>A maps to NM_006420.2 Q627Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:47587655 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr20:47567864 C>T maps to NM_006420.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr4:153831238 G>T maps to NM_001025595.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr4:153803903 G>A maps to NM_001025595.1 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr11:6498958 C>A maps to NM_012402.2 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr20:62338383 G>A maps to NM_003224.3 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr20:62337723 C>T maps to NM_003224.3 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr14:68086726 C>T maps to NM_001172.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr14:68112473 C>T maps to NM_001172.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr14:68117440 C>A maps to NM_001172.3 S290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr3:121305252 C>T maps to NM_001012659.1 Q252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr11:46701309 G>A maps to NM_004308.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:46702859 G>A maps to NM_004308.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:46703682 G>A maps to NM_004308.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr4:148743973 G>A did not map to a codon.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr4:148993172 G>T maps to NM_024605.3 E768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr15:32917776 G>T maps to NM_014783.3 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr15:32929005 C>T maps to NM_014783.3 Q678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr10:32098164 G>A maps to NM_018287.5 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:32109374 G>A maps to NM_018287.5 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr10:32115304 C>T maps to NM_018287.5 W486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr10:32120667 G>A maps to NM_018287.5 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr10:32197272 G>A maps to NM_018287.5 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr2:144194528 C>T maps to NM_018460.3 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:143959729 C>T maps to NM_018460.3 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr16:24990326 C>T did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr16:24988547 G>A maps to NM_001006634.1 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr16:24958916 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr10:99019305 G>A maps to NM_032900.4 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr10:99003769 A>T maps to NM_032900.4 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr10:99003772 G>A maps to NM_032900.4 H379H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr10:98994982 C>G maps to NM_032900.4 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr10:99025635 G>A maps to NM_032900.4 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr10:99025872 G>A maps to NM_032900.4 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr11:110454286 G>A maps to NM_020809.2 N530N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:110451668 C>T maps to NM_020809.2 K667K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:110582891 C>T maps to NM_020809.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr11:110450777 A>G maps to NM_020809.2 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr10:24880172 G>A maps to NM_020824.3 V1377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:24889678 G>A maps to NM_020824.3 R1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr10:24883911 C>G maps to NM_020824.3 L1281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr10:49658320 G>C maps to ENST00000417912 Y633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr10:49667752 G>A maps to ENST00000417912 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:86893234 C>T maps to NM_001025616.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:69002356 G>T maps to NM_001007231.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:69053292 C>G maps to NM_001007231.2 V636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:69045055 C>T maps to NM_001007231.2 D311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:69002383 G>A maps to NM_001007231.2 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr2:69002500 G>A maps to NM_001007231.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr5:142150445 C>T maps to NM_015071.4 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:142283102 A>C did not map to a codon.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr5:142586867 C>G maps to NM_015071.4 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr5:142435651 G>T did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr5:142500654 C>A maps to NM_015071.4 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr5:142437205 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr5:142500672 G>A maps to NM_015071.4 Q553Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:43481020 G>A maps to ENST00000428638 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:43473609 C>G maps to ENST00000428638 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr18:6859844 C>T maps to ENST00000400091 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr18:6890487 G>A maps to ENST00000400091 K598K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:94674862 G>A maps to NM_004815.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:94650458 G>T maps to NM_004815.3 S693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:94640030 G>A maps to NM_004815.3 D1060D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:94650484 G>A maps to NM_004815.3 I684I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr1:161022266 C>T maps to NM_001025598.1 E301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr1:161017863 G>T maps to NM_001025598.1 R983R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:161017654 G>C maps to NM_001025598.1 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:161017553 G>T maps to NM_001025598.1 S1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr3:119134791 C>G maps to NM_020754.2 S1339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr3:119120885 G>A maps to NM_020754.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr3:119112387 C>G maps to NM_020754.2 S319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr3:119133814 G>T maps to NM_020754.2 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr3:119101137 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:119102030 C>T maps to NM_020754.2 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr3:119121137 G>A maps to NM_020754.2 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr3:119135095 G>A maps to NM_020754.2 G1440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr11:128844361 T>C maps to NM_001142685.1 G896G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr11:128844062 G>C maps to NM_001142685.1 S996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr11:128844493 A>C maps to NM_001142685.1 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:128857988 G>A maps to NM_001142685.1 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:128842724 G>A maps to NM_001142685.1 Q1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr11:129061979 G>A maps to NM_001142685.1 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr11:128840031 C>T maps to NM_001142685.1 L1678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:128842773 G>C maps to NM_001142685.1 V1195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr11:129062020 G>A maps to NM_001142685.1 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr11:128851831 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr11:128839533 G>A maps to NM_001142685.1 G1844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr11:128856448 C>T maps to NM_001142685.1 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr19:36278139 G>A maps to ENST00000007510 P891P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr19:36271710 G>A maps to ENST00000007510 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr19:36273702 G>A maps to ENST00000007510 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr19:36278924 C>G maps to ENST00000007510 S1153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr19:36278973 C>T maps to ENST00000007510 Y1169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:36271180 C>T maps to ENST00000007510 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr23:130220620 A>G did not map to a codon.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr23:130219950 A>T did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr23:130220600 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr23:130218958 A>C did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr8:145806414 C>T maps to NM_025251.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr8:145757707 C>T maps to NM_025251.1 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr8:145771083 C>T maps to NM_025251.1 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr8:145772681 G>A maps to NM_025251.1 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr23:153179045 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:153186823 G>A did not map to a codon.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr23:153178220 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:153186956 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr14:32562187 G>A maps to NM_001030055.1 K771K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr14:32562940 T>C maps to NM_001030055.1 H1022H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr14:32563174 A>G maps to NM_001030055.1 K1100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr14:32560833 C>G maps to NM_001030055.1 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:11204417 T>C did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr23:11272741 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:11157175 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:11162005 G>A did not map to a codon.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr23:11197511 C>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:11206911 G>C did not map to a codon.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr23:11206893 G>A did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:11197422 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr23:11156992 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr22:45241211 G>C maps to ENST00000352766 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr22:45241146 A>C did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr22:45241151 C>G maps to ENST00000352766 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:57870233 C>T maps to ENST00000393797 K414K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr12:57867439 G>C maps to ENST00000393797 S747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:57870685 G>A maps to ENST00000393797 R382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr12:57866332 C>T maps to ENST00000393797 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr17:79826898 G>A maps to NM_004309.4 Y156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:15100818 T>C maps to NM_001175.4 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:42402701 C>G maps to NM_199002.1 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr19:42406711 G>A maps to NM_199002.1 Q524Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:42407863 C>G maps to NM_199002.1 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr8:1841802 G>A maps to ENST00000398564 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr8:1893768 C>G maps to ENST00000398564 L1140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr8:1876681 A>G maps to ENST00000398564 E954E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr8:1846618 C>T maps to ENST00000398564 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr8:1905266 G>A maps to ENST00000398564 L1316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr8:1876768 G>A maps to ENST00000398564 V983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr1:18023718 C>T maps to NM_018125.3 R1228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:17965154 C>G maps to NM_018125.3 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:17975109 C>T maps to NM_018125.3 F778F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:17981179 C>G maps to NM_018125.3 S815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr1:17942674 C>T maps to NM_018125.3 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr1:18023481 C>T maps to NM_018125.3 D1149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:17958825 C>G maps to NM_018125.3 S532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:156918211 C>T maps to NM_198236.1 E668E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr1:156913742 G>T maps to NM_198236.1 I1073I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr1:156911197 G>A maps to NM_198236.1 F1160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:156912572 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:156955940 T>C maps to NM_198236.1 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:156926340 G>A maps to NM_198236.1 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr11:120336052 A>G maps to NM_015313.2 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr11:120317776 C>A maps to NM_015313.2 A524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr11:120312887 C>T maps to NM_015313.2 Q427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr11:120347413 C>T maps to NM_015313.2 Q1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr17:8218754 C>T maps to NM_173728.3 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:3389955 G>A did not map to a codon.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr1:3394587 G>A maps to NM_014448.3 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:3397027 G>A maps to NM_014448.3 E669E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr1:3394473 G>A maps to NM_014448.3 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr1:3390079 G>A maps to NM_014448.3 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:3389986 G>A maps to NM_014448.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:73066681 C>G maps to NM_014786.3 L1186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr11:73067779 G>A maps to NM_014786.3 L1289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr11:73076735 C>T maps to NM_014786.3 I1913I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr11:73066579 C>T maps to NM_014786.3 F1152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:7518412 C>G maps to NM_001130955.1 S451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:7518503 C>G maps to NM_001130955.1 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr1:16534529 C>T maps to NM_153213.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:16534655 G>A maps to NM_153213.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:16534658 G>A maps to NM_153213.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:16532691 G>C maps to NM_153213.3 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr1:16534270 C>T maps to NM_153213.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr1:16535330 G>A maps to NM_153213.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr1:155931989 G>A maps to NM_001162383.1 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:155921969 G>A maps to NM_001162383.1 R681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr1:155922417 C>A did not map to a codon.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr1:155935539 C>A maps to NM_001162383.1 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr3:56789067 C>A maps to NM_001128615.1 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:143884108 G>A maps to NM_001003702.2 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:148999930 C>T maps to NM_001001669.2 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr5:149011678 G>A maps to NM_001001669.2 Q651Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr4:106510537 C>G maps to ENST00000420470 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr2:131799408 C>T maps to NM_015320.2 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr2:131797740 C>A maps to NM_015320.2 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:131797928 G>A maps to NM_015320.2 Q340Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr2:131799444 C>T maps to NM_015320.2 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr7:144075918 G>A maps to NM_005435.3 E1532E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr23:135772878 G>C did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:135754202 T>C did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr23:135761776 G>A did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:135825920 G>C did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:135862909 C>G did not map to a codon.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr23:135825835 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr23:135767972 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:135751655 G>C did not map to a codon.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr13:111870216 C>G maps to NM_001113511.1 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr23:62885821 G>A did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr23:62885869 C>G did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr23:62926190 C>T did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr1:27087457 C>T maps to NM_006015.4 Q678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr1:27100389 G>A did not map to a codon.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr1:27100389 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr1:27099396 C>T maps to NM_006015.4 Q1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:27105792 G>T maps to NM_006015.4 E1802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:27087920 C>T maps to NM_006015.4 I736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:27056159 C>T maps to NM_006015.4 Q386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:27106491 G>T maps to NM_006015.4 E2035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:27057834 C>T maps to NM_006015.4 Q515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:27101308 G>T maps to NM_006015.4 E1531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr1:27059259 C>T maps to NM_006015.4 Q633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:27058056 C>T maps to NM_006015.4 Q589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr1:27099360 C>T maps to NM_006015.4 Q1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr1:27107007 C>T maps to NM_006015.4 Q2207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr1:27087416 C>G maps to NM_006015.4 S664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:27100194 C>T maps to NM_006015.4 Q1331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:27106353 C>T maps to NM_006015.4 R1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr1:27106860 C>T maps to NM_006015.4 R2158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr1:27057726 C>T maps to NM_006015.4 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr1:27097664 C>G maps to NM_006015.4 S1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr1:27087557 C>G maps to NM_006015.4 S711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:27094312 G>A maps to NM_006015.4 K1007K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:27097664 C>A maps to NM_006015.4 S1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr1:27057960 C>T maps to NM_006015.4 Q557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:27099987 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr1:27057987 C>T maps to NM_006015.4 Q566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:27094373 C>T maps to NM_006015.4 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr1:27101053 C>T maps to NM_006015.4 R1446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr1:27056180 C>T maps to NM_006015.4 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr1:27097664 C>G maps to NM_006015.4 S1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr1:27094469 G>T maps to NM_006015.4 E1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr1:27057641 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr1:27092946 G>A did not map to a codon.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr1:27101467 C>T maps to NM_006015.4 Q1584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr1:27059263 C>G maps to NM_006015.4 S634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr1:27100374 C>T maps to NM_006015.4 Q1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr1:27057946 C>G maps to NM_006015.4 S552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:27059193 C>T maps to NM_006015.4 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:27097693 C>T maps to NM_006015.4 Q1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr1:27089675 C>T maps to NM_006015.4 Q878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr1:27092808 C>T maps to NM_006015.4 Q944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr1:27100987 C>T maps to NM_006015.4 Q1424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr1:27057825 C>T maps to NM_006015.4 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr1:27101295 G>A maps to NM_006015.4 V1526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr1:27100374 C>T maps to NM_006015.4 Q1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr1:27106538 G>A maps to NM_006015.4 W2050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:27092808 C>T maps to NM_006015.4 Q944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:27094385 G>T maps to NM_006015.4 E1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:27056180 C>T maps to NM_006015.4 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr1:27099320 G>A maps to NM_006015.4 G1186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr1:27094385 G>T maps to NM_006015.4 E1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:27057810 C>T maps to NM_006015.4 Q507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:27094354 G>A maps to NM_006015.4 K1021K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:27089462 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr1:27087954 C>T maps to NM_006015.4 Q748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:27059212 C>G maps to NM_006015.4 S617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:27107179 C>A maps to NM_006015.4 S2264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:27059263 C>G maps to NM_006015.4 S634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr1:27101316 G>A maps to NM_006015.4 L1533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:27101299 C>T maps to NM_006015.4 R1528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:27087457 C>T maps to NM_006015.4 Q678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:27106511 G>A maps to NM_006015.4 V2041V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr6:157517417 C>T maps to ENST00000367148 Q1368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:157256699 C>G maps to ENST00000367148 S663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr6:157528458 G>T maps to ENST00000367148 E2102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr6:157150435 C>T maps to ENST00000367148 Q540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr6:157150396 C>T maps to ENST00000367148 Q527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr6:157222595 G>T maps to ENST00000367148 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr6:157522063 C>T maps to ENST00000367148 Q1486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr6:157256608 C>T maps to ENST00000367148 Q633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr6:157470082 C>T maps to ENST00000367148 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr6:157505528 G>A maps to ENST00000367148 G1210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr6:157150429 C>T maps to ENST00000367148 Q538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:157502140 G>C maps to ENST00000367148 T1098T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:157527626 C>T maps to ENST00000367148 F1824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:157525062 G>A maps to ENST00000367148 W1693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr12:46231477 G>T maps to NM_152641.2 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr12:46244183 C>T maps to NM_152641.2 Q760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr12:46243483 C>T maps to NM_152641.2 Q613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:46287314 C>T maps to NM_152641.2 R1754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr12:46245473 G>T maps to NM_152641.2 G1190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr12:46245274 G>T maps to NM_152641.2 G1123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr12:46246373 G>T maps to NM_152641.2 G1490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:46244138 C>T maps to NM_152641.2 Q745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:46244405 C>T maps to NM_152641.2 Q834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr12:46243817 G>A did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr12:46245082 G>A maps to NM_152641.2 L1059L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr12:46125014 C>T maps to NM_152641.2 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr12:46245433 T>C maps to NM_152641.2 V1176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr12:46230743 C>T maps to NM_152641.2 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr12:46231348 C>T maps to NM_152641.2 Q397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:46243449 G>A maps to NM_152641.2 R601R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:46245203 C>T maps to NM_152641.2 Q1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr12:46298715 G>A did not map to a codon.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr12:46230578 G>A maps to NM_152641.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr12:46298725 G>A maps to NM_152641.2 K1791K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr12:46298732 G>T maps to NM_152641.2 E1794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr12:46231141 G>C maps to NM_152641.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr19:965072 C>T maps to NM_005224.2 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr19:971891 C>T maps to NM_005224.2 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr19:972045 C>G maps to NM_005224.2 S588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr15:74888012 C>T maps to ENST00000395077 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr9:34622476 T>C maps to NM_001017363.1 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr9:34623554 G>A maps to NM_001017363.1 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr9:34622032 G>A maps to NM_001017363.1 N374N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr14:58831817 C>G maps to NM_002892.3 S1004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr14:58785308 G>C maps to NM_002892.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:235357526 C>G did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:235377118 G>A maps to NM_016374.5 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:235383126 C>A maps to NM_016374.5 E522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr2:97216889 C>T maps to NM_212481.1 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:97215119 C>T maps to NM_212481.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:97213235 G>A maps to NM_212481.1 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:63852164 G>C maps to NM_032199.2 V981V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:63700147 C>T maps to NM_032199.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:63817046 G>T maps to NM_032199.2 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:63851945 G>C maps to NM_032199.2 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr3:49004676 C>T maps to NM_006321.2 C169C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:49017851 C>T maps to NM_006321.2 Q394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr3:49006037 G>T maps to NM_006321.2 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr13:50204622 C>T maps to NM_138450.5 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr13:50204891 C>T maps to NM_138450.5 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:100229173 G>A did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr23:100240782 T>C did not map to a codon.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr23:100240711 G>C did not map to a codon.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr23:100240720 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:100243242 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr23:100242378 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr3:93761857 G>C did not map to a codon.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr3:160395580 G>T maps to NM_025047.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:160395610 C>T maps to NM_025047.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr17:79649080 C>T maps to NM_001040025.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr11:64781687 C>G maps to NM_001667.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr7:12728199 G>A maps to NM_005738.4 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr2:235405158 G>A maps to ENST00000339728 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:235404738 G>A maps to ENST00000339728 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:41477528 G>A maps to NM_001661.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr17:41477291 C>T maps to NM_001661.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr3:97516866 G>C did not map to a codon.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr16:18810023 G>A maps to NM_015161.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:69153636 G>A maps to NM_006407.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:153575446 G>A maps to NM_152522.4 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr3:5213864 C>T maps to ENST00000438743 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:66517677 G>A maps to NM_018120.4 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr7:102727177 G>C maps to NM_031905.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr6:109282853 G>C maps to NM_032131.4 V665V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr10:23321934 C>T maps to NM_173081.3 R798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr10:23250839 G>T maps to NM_173081.3 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:23257233 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:23297818 T>C maps to NM_173081.3 N668N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr10:23292273 G>A maps to NM_173081.3 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr10:23287283 C>G maps to NM_173081.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr10:28196615 G>C maps to NM_018076.2 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr10:28101441 C>G maps to NM_018076.2 *1045S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr10:28233159 G>A maps to NM_018076.2 I578I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr10:28283954 C>T maps to NM_018076.2 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:31473662 C>T maps to ENST00000408912 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr16:31475999 G>A maps to ENST00000408912 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr16:31470856 G>A maps to ENST00000408912 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:31470892 C>T maps to ENST00000408912 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr16:31476377 A>G maps to NM_024742.2 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr19:19168394 C>G maps to ENST00000392336 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr19:19154810 G>C maps to ENST00000392336 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr19:19166159 G>A maps to ENST00000392336 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:73106391 G>A maps to NM_024585.2 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:73106397 G>A maps to NM_024585.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr3:137991853 C>T maps to ENST00000469044 R509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr3:137956399 C>T maps to ENST00000469044 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr3:137983014 C>G maps to ENST00000469044 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr3:137956209 G>A maps to ENST00000469044 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr2:232156133 C>T maps to ENST00000359743 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:232143142 C>A maps to ENST00000359743 S508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:232143131 C>T maps to ENST00000359743 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr2:232079644 C>A maps to ENST00000359743 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:232100045 C>G maps to ENST00000359743 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr23:100807940 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr23:100808025 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:100808514 T>C did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr23:100808510 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr23:100912250 C>G did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:100912133 C>T did not map to a codon.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr23:100911505 C>T did not map to a codon.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr23:100912482 C>T did not map to a codon.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr23:100910851 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:100911859 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr23:100911086 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:100912203 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr23:100911929 G>T did not map to a codon.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:100880169 C>A did not map to a codon.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:100880624 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr23:100880989 C>T did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr23:100880049 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr23:101857612 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr23:101857567 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:101857852 C>A did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr23:101857860 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr23:101857578 A>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr23:100871399 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr23:100871234 C>A did not map to a codon.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr23:100871490 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr23:100871338 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:150786622 G>C maps to NM_001668.3 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:80767364 C>G maps to NM_014862.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr15:80872757 A>G maps to NM_014862.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr11:13393821 C>A maps to ENST00000403290 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:13407234 G>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr11:13380067 C>T maps to ENST00000403290 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:27573405 G>T maps to NM_020183.3 E618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:27553557 G>A maps to NM_020183.3 K337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:27573350 C>T maps to NM_020183.3 F599F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr7:98951612 G>A maps to NM_006409.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:98951562 G>T maps to NM_006409.3 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr7:98951687 G>T maps to NM_006409.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr7:98988644 C>T maps to NM_005720.2 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr2:219114618 G>T maps to NM_005731.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr12:110874485 G>A maps to NM_005719.2 C85C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:9843422 C>T maps to NM_001198793.1 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:9845654 C>T maps to ENST00000453882 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:183604788 C>A maps to ENST00000294742 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr9:127637309 T>C maps to NM_030978.1 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr3:169485492 A>G maps to NM_032487.4 C282C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:169487203 G>A maps to NM_032487.4 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr3:35729369 C>G maps to ENST00000458225 S134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr3:35835347 G>C maps to ENST00000458225 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr11:74988492 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr17:4620510 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr17:4621907 G>A maps to ENST00000412477 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr9:140508608 C>G maps to NM_152285.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr19:18120727 C>T maps to NM_015683.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr19:18119169 C>T maps to NM_015683.1 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr5:90669562 G>A maps to NM_020801.2 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr5:90672536 C>T maps to NM_020801.2 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr19:4891249 C>T maps to NM_001080523.1 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr19:4891333 C>G maps to NM_001080523.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr22:51064426 G>T maps to ENST00000395624 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr22:51065113 C>T maps to ENST00000395624 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr5:78135223 C>A maps to NM_000046.3 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:78280774 G>A maps to NM_000046.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr23:2828743 C>G did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr23:2826823 T>C did not map to a codon.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr23:2827941 C>A did not map to a codon.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr23:2835842 A>G did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:2836236 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr23:2825475 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr23:2838726 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr23:2825534 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr23:2827913 C>G did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:2876406 G>A did not map to a codon.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr23:2871264 C>T did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr23:2861117 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:2861178 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr23:3002366 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr23:3030587 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:3002381 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr23:3002514 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:66352861 C>A maps to NM_014960.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr17:66366604 C>T maps to NM_014960.3 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr17:66352861 C>G maps to NM_014960.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:2945384 T>C did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:2942119 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr23:2933397 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr23:2928166 G>C did not map to a codon.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr23:2936712 T>G did not map to a codon.
Sequencing variant TCGA-XF-AAMJ-01A-11D-A42E-08 chr23:2933064 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr5:149677613 G>A maps to NM_001012301.2 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr5:149677094 G>A maps to NM_001012301.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr5:149677552 G>A maps to NM_001012301.2 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr5:149681714 C>A maps to NM_001012301.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr5:149677421 C>A maps to NM_001012301.2 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr4:114823587 C>A maps to NM_024590.3 G548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr4:114824433 G>A maps to NM_024590.3 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:94891053 G>A maps to NM_198150.2 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr11:3681333 G>A maps to NM_004314.2 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr11:3681294 C>T maps to NM_004314.2 H182H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:14993595 G>A maps to NM_021071.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr12:14982331 G>A maps to NM_021071.2 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:3660920 G>A maps to NM_001079536.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:44401688 C>A maps to ENST00000438616 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr1:231132939 C>G maps to NM_022786.1 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr22:19965030 G>A maps to NM_001670.2 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:19960540 C>T maps to NM_001670.2 A819A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:19978248 G>A maps to NM_001670.2 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr22:19969578 C>T maps to NM_001670.2 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr22:19961658 C>T maps to NM_001670.2 Q688Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr22:19968924 G>A maps to NM_001670.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr23:25028405 T>A did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:25025277 G>A did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr10:104636742 T>C maps to NM_020682.3 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr10:104632203 G>T did not map to a codon.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr11:122953895 T>A maps to NM_024769.2 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr11:122945489 C>G maps to NM_024769.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr8:131138242 G>A maps to NM_018482.2 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:131073250 C>T maps to NM_018482.2 Q922Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:131200402 G>A maps to NM_018482.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:131140336 C>T did not map to a codon.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr8:131172135 C>T maps to NM_018482.2 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:9540886 G>A maps to NM_003887.2 T917T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr2:9515007 G>T maps to NM_003887.2 G561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:9474902 C>G maps to NM_003887.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr2:9519150 C>G maps to NM_003887.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:9540172 G>A maps to NM_003887.2 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:9540150 G>C did not map to a codon.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:23768755 G>C maps to NM_017707.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:23763090 G>A maps to NM_017707.3 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:23782406 G>A maps to NM_017707.3 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr1:23763472 G>C maps to NM_017707.3 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr1:23769092 C>T maps to NM_017707.3 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:23767921 G>A maps to NM_017707.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:239353165 C>T maps to NM_001040445.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr7:150878046 G>A maps to ENST00000422024 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr7:150878037 C>G maps to ENST00000422024 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr7:150878189 G>A maps to ENST00000422024 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr7:150878190 G>A maps to ENST00000422024 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr7:150873258 G>A maps to ENST00000422024 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:15311337 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr23:15307697 G>A did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr23:15320871 G>A did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:15332509 A>G did not map to a codon.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr23:15311406 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr23:63445138 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr23:63445341 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr10:5682737 G>A maps to NM_024701.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:57312521 C>T maps to ENST00000295941 R2808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr7:123269343 G>C maps to NM_080928.3 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr17:42248267 G>A maps to NM_080863.4 R37R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ZF-AA51-01A-21D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:237103688 C>T maps to NM_212556.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr14:94404062 G>C maps to ENST00000434324 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr7:95157437 C>T maps to NM_016116.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr9:132404197 G>T maps to NM_017873.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr9:132400069 C>G maps to NM_017873.2 *422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr12:48547242 G>A maps to NM_024095.3 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr12:48543478 G>A maps to NM_024095.3 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr23:15266881 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:15262641 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr22:30198079 G>A maps to NM_032204.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:30188507 G>A maps to NM_032204.3 Q646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr22:30186504 C>G maps to NM_032204.3 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr22:30221763 G>C maps to NM_032204.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr22:30185084 C>A maps to NM_032204.3 E731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr22:30186465 G>A maps to NM_032204.3 A698A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr6:101296315 G>T maps to NM_006828.2 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr6:101312008 G>A maps to NM_006828.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:101248282 A>C maps to NM_006828.2 Y340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr6:101246630 G>A maps to NM_006828.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr6:101103592 G>A maps to NM_006828.2 I935I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr6:101246630 G>C maps to NM_006828.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr6:100988254 T>C maps to NM_006828.2 E1853E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr6:101110331 C>T maps to NM_006828.2 Q789Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:108169066 G>A maps to NM_203436.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr6:119226947 G>A maps to NM_014034.2 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:14232406 G>C maps to NM_018154.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:14232457 G>A maps to NM_018154.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:14231398 C>A maps to NM_018154.2 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr17:7080604 G>A maps to NM_001671.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr17:7077347 C>T maps to NM_001671.3 W211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:7010562 G>A maps to NM_080912.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:7005485 G>A maps to NM_080912.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:155319162 C>T maps to ENST00000368346 V2508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:155451156 G>A maps to ENST00000368346 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr1:155449221 G>A maps to ENST00000368346 Q1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:155490914 C>T maps to ENST00000368346 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:155319215 G>A maps to ENST00000368346 L2491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:155322526 C>A maps to ENST00000368346 E2451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:155340688 G>A maps to ENST00000368346 Q2145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:155449332 G>A maps to ENST00000368346 Q1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:65554626 C>G maps to NM_000048.3 S336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr7:65553884 C>T maps to NM_000048.3 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr23:1752142 C>A did not map to a codon.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr23:1553954 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr23:1540662 A>G did not map to a codon.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr23:1553954 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr23:1571709 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr23:1540621 C>G did not map to a codon.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr23:1522381 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:1546655 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:1531684 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:1540606 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:1540608 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr23:1531717 C>A did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:12848429 G>A maps to NM_004317.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr2:190532078 C>T maps to NM_019048.2 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr2:190532555 C>T maps to NM_019048.2 Q511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:3397674 C>A maps to NM_000049.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:104571062 C>T maps to NM_001080464.1 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr14:104552128 G>T maps to NM_001080464.1 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr14:104552112 G>A maps to NM_001080464.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:62438578 C>T maps to NM_004318.3 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr8:62559381 C>T maps to NM_004318.3 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr16:29916254 C>T maps to NM_181718.3 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr16:29912567 C>G maps to NM_181718.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr16:29913071 C>T maps to NM_181718.3 C260C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr22:26830195 C>T maps to NM_020437.4 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr22:26838527 G>A maps to NM_020437.4 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:197073958 C>T maps to NM_018136.4 W1474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:197070598 C>T maps to NM_018136.4 Q2594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:197060161 G>A maps to NM_018136.4 R3152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:197069680 T>C maps to NM_018136.4 K2900K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:197070085 C>T maps to NM_018136.4 K2765K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:197071384 T>A maps to NM_018136.4 R2332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:197072566 C>T maps to NM_018136.4 R1938R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:197059407 G>C maps to NM_018136.4 L3249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr1:197098361 G>C maps to NM_018136.4 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:197063310 C>A did not map to a codon.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr9:95219644 G>T maps to NM_017680.4 Y356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr2:70188016 C>G maps to NM_152792.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr2:70188394 G>C maps to NM_152792.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:70187883 G>A maps to NM_152792.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr2:70188814 C>T maps to NM_152792.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr17:79970156 C>T maps to ENST00000306729 Q451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr17:79941433 C>T maps to ENST00000306729 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:79941447 C>T maps to ENST00000306729 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr17:79970158 G>A maps to ENST00000306729 Q451Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr17:79943432 C>T maps to ENST00000306729 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:79954409 C>T maps to ENST00000306729 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:62124475 G>C maps to NM_025080.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:62124487 C>T maps to NM_025080.3 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr11:62159066 G>A maps to NM_025080.3 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr11:62159689 C>T maps to NM_025080.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:133370344 C>G maps to NM_000050.4 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:96798411 C>A maps to NM_001002036.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:96789737 G>A maps to NM_001002036.3 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr2:96799203 G>A maps to NM_001002036.3 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr1:176863733 G>C maps to ENST00000281881 P976P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:176903363 C>T maps to ENST00000281881 E873E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:176998853 C>A maps to ENST00000281881 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:177030360 C>T maps to ENST00000281881 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:176833620 G>C maps to ENST00000281881 L1236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr1:177030252 C>T maps to ENST00000281881 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr1:176845724 G>A maps to ENST00000281881 S1145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:176998792 G>T maps to ENST00000281881 S366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:176913087 G>T maps to ENST00000281881 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:177133536 G>A maps to ENST00000281881 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:177030375 G>A maps to ENST00000281881 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:119770437 T>G maps to ENST00000313400 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr9:119976745 A>G maps to ENST00000313400 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr20:30956841 C>G maps to ENST00000375687 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr20:31017810 C>T maps to ENST00000375687 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr20:31021690 A>T maps to ENST00000375687 K564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:31022244 C>G maps to ENST00000375687 S577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr20:31021534 C>T maps to ENST00000375687 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr20:31021331 C>G maps to ENST00000375687 S444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr20:31022852 C>T maps to ENST00000375687 Q780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr20:31024777 C>T maps to ENST00000375687 L1421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr20:31021671 C>G maps to ENST00000375687 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr20:31022276 C>T maps to ENST00000375687 Q588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr20:31016180 C>T maps to ENST00000375687 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr20:31022287 C>A maps to ENST00000375687 Y591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr20:31025056 C>T maps to ENST00000375687 I1514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr20:31024798 T>G maps to ENST00000375687 S1428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:25994387 G>T maps to NM_018263.4 S142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:25990451 T>A maps to NM_018263.4 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr2:25972632 G>A maps to NM_018263.4 Q598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr2:25990543 G>C maps to NM_018263.4 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:25972726 G>C maps to NM_018263.4 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:25972942 G>A maps to NM_018263.4 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr2:25982411 G>T maps to NM_018263.4 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:25990550 G>A maps to NM_018263.4 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:25965512 C>T maps to NM_018263.4 V1231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr2:25978948 G>C maps to NM_018263.4 S325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr2:25994350 G>A maps to NM_018263.4 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr2:25978891 G>C maps to NM_018263.4 S344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr2:25990522 G>C maps to NM_018263.4 S235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr18:31325634 C>T maps to NM_030632.1 P1941P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr18:31318936 A>G maps to NM_030632.1 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:31311951 A>G maps to NM_030632.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr18:31325871 A>G maps to NM_030632.1 P2020P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr18:31326429 A>T maps to NM_030632.1 A2206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr18:31323531 T>G maps to NM_030632.1 V1240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr7:117060281 C>T maps to NM_130768.2 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr7:117023079 A>G maps to NM_130768.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr10:89544296 C>T maps to NM_032810.2 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr8:124382175 A>G maps to NM_014109.3 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr8:124371476 T>A maps to NM_014109.3 K456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr8:124383929 C>A maps to NM_014109.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr8:124408510 G>C maps to NM_014109.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr8:124346179 G>C maps to NM_014109.3 S1139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr8:124351686 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr8:124360434 C>A maps to NM_014109.3 E629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr8:124382175 A>G maps to NM_014109.3 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr8:124369976 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:24011421 G>C maps to NM_017552.1 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr2:24056802 G>A maps to NM_017552.1 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:1451458 C>G maps to NM_018188.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:1455590 G>A maps to NM_018188.3 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:1417557 G>A maps to NM_031921.4 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr1:1421163 C>G maps to NM_031921.4 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:1412672 G>A maps to NM_031921.4 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr1:1390874 C>T maps to NM_001039211.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:29163029 T>G maps to NM_024857.3 L644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr17:29187575 G>T maps to NM_024857.3 E1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr17:29220309 A>T did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr17:29162761 C>T maps to NM_024857.3 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr17:29162511 G>T maps to NM_024857.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr19:3907798 G>A maps to NM_033064.4 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr19:3905457 G>T maps to NM_033064.4 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr10:123629520 C>T maps to NM_001001976.1 E325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:123670501 G>A maps to NM_001001976.1 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr10:123596254 G>C maps to NM_001001976.1 S412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr10:123687389 G>A maps to NM_001001976.1 Y25Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr10:123600703 G>A maps to NM_001001976.1 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:51207890 C>T maps to NM_005171.4 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr12:51208090 G>A maps to NM_005171.4 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr2:175979452 T>C maps to NM_001880.2 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr22:39918444 G>A maps to NM_182810.1 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr22:39918552 G>A maps to NM_182810.1 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr22:39917470 G>C maps to NM_182810.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:161753802 C>T maps to NM_007348.2 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:161833096 C>T maps to NM_007348.2 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr1:161761286 G>A maps to NM_007348.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr1:161789556 G>A maps to NM_007348.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:161928234 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr1:161753802 C>T maps to NM_007348.2 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr6:32086783 G>A maps to NM_004381.4 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr6:32095972 C>G maps to NM_004381.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr6:32095527 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr6:32083533 G>C maps to NM_004381.4 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:32089081 G>C maps to NM_004381.4 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:53911119 G>C maps to NM_001130059.1 S429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:53994748 C>A maps to NM_001130059.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr12:53917061 A>C maps to NM_001130059.1 L422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr12:14650793 T>G maps to NM_018179.3 A1200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr12:14633974 C>T maps to NM_018179.3 Q1046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr12:14649243 C>T maps to NM_018179.3 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:14578262 G>T maps to NM_018179.3 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr12:14650677 C>T maps to NM_018179.3 Q1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr16:10566011 G>A maps to NM_024997.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr16:10551355 C>A maps to NM_024997.2 S441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr2:234183393 G>T maps to ENST00000392018 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:234198933 T>C maps to ENST00000392018 I472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:72533552 G>T maps to NM_033388.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr11:64669801 G>A maps to ENST00000421419 I1280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr11:64681297 C>A maps to ENST00000421419 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:64669496 G>A maps to ENST00000421419 G1354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:64670062 G>C maps to ENST00000421419 L1234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr11:64678574 G>A maps to ENST00000421419 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr11:64680856 C>A maps to ENST00000421419 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr11:64674209 G>A maps to ENST00000421419 V970V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr11:64675046 G>T maps to ENST00000421419 S866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr14:96777504 C>T maps to NM_018036.5 Q1370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:96807894 G>A maps to NM_018036.5 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr14:96757943 G>A maps to NM_018036.5 R1858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:96807900 C>T maps to NM_018036.5 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr14:96829296 G>T maps to NM_018036.5 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:96756085 G>C maps to NM_018036.5 P1971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr14:96798942 G>C maps to NM_018036.5 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:107381401 T>C did not map to a codon.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr23:107372016 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:242594012 C>G maps to ENST00000337606 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:63269498 C>G maps to NM_032852.2 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr1:63282348 G>A maps to NM_032852.2 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:63284711 C>G maps to NM_032852.2 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr19:10662921 G>A maps to NM_032885.4 K388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr19:10663607 G>T maps to NM_032885.4 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:10662772 C>T maps to NM_032885.4 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:106634468 C>G maps to NM_004849.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:11404345 G>A maps to NM_006395.2 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr3:11340867 T>C maps to NM_006395.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:220085579 G>A maps to NM_024085.3 F801F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr2:220087387 C>T maps to NM_024085.3 Q609Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:220089300 G>C maps to NM_024085.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr7:150715786 G>A maps to NM_173681.5 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr7:150715810 G>C maps to NM_173681.5 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr7:150713863 G>A maps to NM_173681.5 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr11:294326 C>T maps to ENST00000409479 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr11:294284 G>A maps to ENST00000409479 V636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:216190857 G>A maps to NM_004044.6 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:216177323 C>T maps to NM_004044.6 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:216213869 C>T maps to NM_004044.6 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr2:216211606 G>A maps to NM_004044.6 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr14:51094843 G>T maps to ENST00000358385 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr14:51081200 C>G maps to ENST00000358385 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr14:51095135 C>T maps to ENST00000358385 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr11:108160487 C>T maps to NM_000051.3 R1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr11:108165782 C>T maps to NM_000051.3 Q1636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:108196790 G>T maps to NM_000051.3 E2272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:108115599 C>T maps to NM_000051.3 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr11:108160393 G>A maps to NM_000051.3 K1434K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr11:108175419 C>T maps to NM_000051.3 Q1839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr11:108196035 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr11:108122623 A>G maps to NM_000051.3 K556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr11:108196124 G>T maps to NM_000051.3 E2221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr11:108206597 T>A maps to NM_000051.3 A2726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:108236127 G>T maps to NM_000051.3 E3022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:108236159 G>A maps to NM_000051.3 V3032V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr11:108204611 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:108175523 T>C maps to NM_000051.3 C1873C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr11:108198370 G>C did not map to a codon.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr11:108128334 T>A did not map to a codon.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr11:108153606 G>A did not map to a codon.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr11:108236220 A>T maps to NM_000051.3 K3053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr11:108151819 C>T maps to NM_000051.3 I1167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr11:108175419 C>T maps to NM_000051.3 Q1839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr11:108155032 C>T maps to NM_000051.3 Q1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr16:81078152 C>T maps to NM_015251.2 Q684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr16:81077749 G>A maps to NM_015251.2 Q549Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:81077670 C>G maps to NM_015251.2 S523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:81078382 G>A maps to NM_015251.2 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr12:7047655 G>T maps to NM_001940.3 E844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr2:85982019 C>T maps to NM_032827.6 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr2:85981371 G>T maps to NM_032827.6 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr15:25924823 C>G maps to NM_024490.3 L1388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr15:25958860 G>A maps to NM_024490.3 A768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:25959010 C>T maps to NM_024490.3 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr15:25953402 G>A maps to NM_024490.3 Q797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr15:25959382 C>T maps to NM_024490.3 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr15:25925425 G>A maps to NM_024490.3 F1236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr15:25958923 C>T maps to NM_024490.3 K747K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr15:25953412 C>G maps to NM_024490.3 R793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr15:26107940 C>T maps to NM_024490.3 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:25959136 G>A maps to NM_024490.3 N676N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr15:25959280 C>T maps to NM_024490.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr15:25940239 G>T maps to NM_024490.3 G938G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr15:25953364 G>A maps to NM_024490.3 R809R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr5:160059240 C>T maps to NM_025153.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr5:160016601 T>C maps to NM_025153.2 T1249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr4:47574246 G>A maps to NM_020453.3 Q1080Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr4:47565596 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr4:47593106 G>C maps to NM_020453.3 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr4:47584074 G>A maps to NM_020453.3 K1249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr4:47574246 G>A maps to NM_020453.3 Q1080Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr4:47559724 A>G maps to NM_020453.3 E623E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr4:47559878 G>T maps to NM_020453.3 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr4:47570897 G>A maps to NM_020453.3 Q966Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:47560282 T>A maps to NM_020453.3 A809A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr13:113532598 G>C maps to NM_015205.2 L1132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr13:113496666 C>T maps to NM_032189.3 R595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr13:113514617 G>A maps to NM_032189.3 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr13:113487178 C>T maps to NM_032189.3 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr13:113513758 C>G maps to NM_032189.3 S907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:182586898 A>C maps to NM_014616.1 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr3:182547495 G>T maps to NM_014616.1 G91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:138886665 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:138914336 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr23:138864737 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:138901549 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr23:138823237 G>A did not map to a codon.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr13:25263510 C>T maps to NM_001185085.1 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr13:25276098 C>A maps to NM_001185085.1 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr13:25283941 G>A maps to NM_001185085.1 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr13:25284983 C>T maps to NM_001185085.1 L990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr13:25274960 G>A maps to NM_001185085.1 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr13:25274888 C>T maps to NM_001185085.1 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr19:19774148 G>T maps to NM_020410.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:19770597 G>A maps to NM_020410.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:19764807 C>T maps to NM_020410.2 V653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:17330837 G>A maps to NM_022089.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:17312614 C>T maps to NM_001141974.1 L1114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:17328813 G>A maps to NM_022089.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:17322646 C>A maps to NM_022089.2 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:17319019 C>G maps to NM_022089.2 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr3:194147856 A>C maps to NM_024524.3 G1024G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr3:194167799 T>C maps to NM_024524.3 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr3:194162095 C>A maps to NM_024524.3 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr3:194150427 G>A maps to NM_024524.3 F951F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:194181395 C>T maps to NM_024524.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr3:194165454 G>A maps to NM_024524.3 R520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr3:193151663 G>A maps to NM_032279.2 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:193120595 G>A maps to NM_032279.2 Q1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr3:193048926 G>A maps to NM_198505.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:193029619 G>A maps to NM_198505.2 N810N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:193042709 G>C maps to NM_198505.2 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr3:193081967 G>A maps to NM_198505.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr3:193036818 A>T maps to NM_198505.2 L665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr3:193044813 G>C maps to NM_198505.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr3:193068957 G>A maps to NM_198505.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:192992878 G>C maps to NM_198505.2 L1203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr1:116931579 C>T maps to NM_000701.7 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:116946595 C>T maps to NM_000701.7 G1014G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr1:116932064 C>T maps to NM_000701.7 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr1:116941292 G>A maps to NM_000701.7 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:160098494 G>A maps to NM_000702.3 K357K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:160104335 C>T maps to NM_000702.3 I630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr1:160097471 C>T maps to NM_000702.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:160104275 G>A maps to NM_000702.3 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:42474361 G>C maps to ENST00000441343 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:42490309 C>T maps to ENST00000441343 K143K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr19:42471440 G>A maps to ENST00000441343 Y991Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:42492626 C>A did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:42482218 G>A maps to ENST00000441343 I604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr1:160151812 C>A maps to NM_144699.3 Y987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr1:160143936 G>A maps to NM_144699.3 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:160136488 G>T maps to NM_144699.3 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr1:160145903 G>A maps to NM_144699.3 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:160136382 G>A maps to NM_144699.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr17:7556776 C>T maps to NM_001678.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:141626054 C>T maps to NM_001679.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr3:141595696 C>G maps to NM_001679.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:141622522 G>A maps to NM_001679.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:119512533 G>C did not map to a codon.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr23:119509291 G>T did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr16:28913401 C>T maps to NM_173201.3 V773V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:28914208 C>T maps to NM_173201.3 I907I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr16:28909388 C>A maps to NM_173201.3 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr12:110765545 C>T maps to NM_170665.3 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr12:110783910 C>G maps to NM_170665.3 V949V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr12:110778543 G>A maps to NM_170665.3 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:110784073 G>C maps to NM_170665.3 V976V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr12:110783085 G>C maps to NM_170665.3 P880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr12:110770985 G>A maps to NM_170665.3 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr12:110777384 C>T maps to NM_170665.3 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:110784079 C>T maps to NM_170665.3 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:3839579 G>A maps to NM_174953.1 F835F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr17:3854916 G>A maps to NM_174953.1 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr17:3850882 G>A maps to NM_174953.1 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr17:3854910 C>T maps to NM_174953.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr17:3840801 G>A maps to NM_174953.1 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr17:3844826 G>C maps to NM_174953.1 S556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:90005095 G>C maps to ENST00000428670 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:89996870 G>A maps to ENST00000428670 I1003I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:89985068 G>A maps to ENST00000428670 R1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:90004245 G>A maps to ENST00000428670 R763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr12:90013954 C>T maps to ENST00000428670 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:10420032 G>A maps to NM_001001331.2 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:10382200 G>A maps to NM_001001331.2 I1035I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr3:10452386 C>T maps to NM_001001331.2 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr3:10401789 G>C maps to NM_001001331.2 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr3:10400479 G>A maps to NM_001001331.2 R677R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr3:10400557 G>A maps to NM_001001331.2 R651R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr3:10417248 C>T maps to NM_001001331.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:10379928 G>A maps to NM_001001331.2 D1117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr3:10401786 G>A maps to NM_001001331.2 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr3:10401564 C>A did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:152818715 G>T did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:152821835 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr23:152815031 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr23:152807361 G>A did not map to a codon.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr23:152807847 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr23:152815127 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:152815060 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr23:152813399 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr23:152818579 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:203667471 A>G maps to NM_001001396.1 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:203696674 G>A maps to NM_001001396.1 R1095R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:203680025 G>A maps to NM_001001396.1 R607R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:203693082 C>T maps to NM_001001396.1 L1033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr1:203681194 G>C maps to NM_001001396.1 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:203676347 G>A maps to NM_001001396.1 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:203669379 G>C maps to NM_001001396.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:203670020 G>T maps to NM_001001396.1 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:203652428 C>T maps to NM_001001396.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr3:130694261 G>A maps to NM_001001486.1 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr3:130656282 C>T maps to NM_001001486.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr3:130653525 C>T maps to NM_001001486.1 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr3:130718462 G>T maps to NM_001001486.1 P863P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr16:84459404 C>A maps to ENST00000416219 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr16:84488488 G>C maps to ENST00000416219 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr16:84442087 C>T maps to ENST00000416219 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr16:84488446 C>T maps to ENST00000416219 I668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr16:84476141 C>A maps to ENST00000416219 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:84485626 G>A maps to ENST00000416219 Q587Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:36054366 C>T maps to NM_000704.2 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:36046678 G>A maps to NM_000704.2 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:36051750 G>A maps to NM_000704.2 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr19:36050018 T>G maps to NM_000704.2 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr19:36045889 G>A maps to NM_000704.2 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr19:36053393 G>A maps to NM_000704.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr18:43668177 G>A maps to NM_001001937.1 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr18:43664328 C>T maps to NM_001001937.1 R527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr12:57039720 G>T maps to NM_001686.3 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:57037666 G>A maps to NM_001686.3 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr12:57037254 C>A maps to NM_001686.3 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr10:7844764 C>T maps to NM_001001973.1 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr1:111992468 G>A maps to NM_001688.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:46973040 C>G maps to NM_005175.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr12:54063048 G>C maps to NM_005176.5 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr12:54063119 G>C maps to NM_005176.5 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr12:54059202 A>G maps to NM_005176.5 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr2:176043903 G>A maps to NM_001689.4 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:176043917 G>A maps to NM_001689.4 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr4:667134 C>T maps to NM_007100.3 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:50779752 C>G maps to NM_001003803.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr14:50788294 G>A maps to NM_001003803.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr14:50788198 A>C did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr19:41944169 C>T maps to ENST00000417807 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:41944202 C>G maps to ENST00000417807 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr23:153662054 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr23:153660651 C>G did not map to a codon.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr23:153664174 A>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:81614038 G>T maps to NM_001017971.1 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:40460058 G>C did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr23:40448291 G>A did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:40460034 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr23:40450512 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr23:40456900 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr17:40642596 T>G maps to NM_001130020.1 Y379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:40629671 C>T maps to NM_001130020.1 Q147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr17:40665985 C>T maps to NM_001130020.1 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr12:124236903 A>T maps to NM_012463.3 G710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr12:124236943 G>T maps to NM_012463.3 E724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr12:124241428 C>T maps to NM_012463.3 V787V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:44442264 C>T maps to NM_004047.3 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr16:2569363 C>T maps to NM_001694.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr16:2569580 G>C maps to NM_001694.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:67514905 G>C maps to NM_004691.4 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr16:67514920 C>T maps to NM_004691.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:113528246 G>A maps to NM_001690.3 Q609Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr3:113524290 G>A maps to NM_001690.3 Q560Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr2:71187067 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:71188790 C>T maps to NM_001692.3 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr2:71185527 A>G maps to NM_001692.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr2:71189918 C>T maps to NM_001692.3 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr2:71189910 G>T maps to NM_001692.3 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr8:20055051 C>T maps to NM_001693.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr8:20069161 G>A did not map to a codon.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr2:10912039 C>T maps to NM_001039362.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr2:10918702 C>T maps to NM_001039362.1 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr14:67805357 C>A maps to NM_015994.3 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr22:18111392 G>A maps to NM_001696.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:117359914 C>T maps to NM_004888.3 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr6:31513917 G>A maps to NM_130463.2 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr1:198505854 C>G did not map to a codon.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr8:54730080 G>A maps to NM_015941.2 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr8:54727251 G>A maps to NM_015941.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr23:77245375 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:77244135 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr23:77275801 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr23:77254159 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr23:77275741 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr23:77268495 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr23:77254134 C>T did not map to a codon.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr23:77268473 A>G did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr23:77271358 A>G did not map to a codon.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr23:77268537 A>G did not map to a codon.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr23:77254177 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:77264600 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:77284935 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr23:77301811 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr13:52544885 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:52548419 C>T maps to NM_000053.2 Q312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr13:52524265 T>C maps to NM_000053.2 G869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:42580378 C>A maps to NM_006095.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr4:42558014 T>C maps to NM_006095.2 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:42415016 G>A maps to NM_006095.2 F1137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr4:42445668 C>T maps to NM_006095.2 W1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:26125474 G>T did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr13:26343234 G>A maps to NM_016529.4 V812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr13:26411383 C>G maps to NM_016529.4 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr13:26043217 C>T maps to NM_016529.4 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr13:26273331 C>T maps to NM_016529.4 Q745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr13:26436455 C>T maps to NM_016529.4 V1031V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr13:26542748 G>A maps to NM_016529.4 E1103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr18:55319835 G>C maps to NM_005603.4 L1047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr18:55359070 G>C maps to NM_005603.4 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr18:55355705 G>A maps to NM_005603.4 F418F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G2-AA3B-01A-11D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr18:55364878 G>C maps to NM_005603.4 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:154317864 C>T maps to NM_020452.3 S879S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr1:154321467 G>T maps to NM_020452.3 L1182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:154317146 C>T maps to NM_020452.3 S757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr19:1789426 G>A maps to NM_138813.2 V926V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:1800006 C>A maps to NM_138813.2 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr19:1789015 C>G maps to NM_138813.2 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:1811503 C>A maps to NM_138813.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr19:1796869 G>C maps to NM_138813.2 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr19:1796806 G>A maps to NM_138813.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:1785275 G>C maps to NM_138813.2 Y1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr19:1785611 G>A maps to NM_138813.2 I1083I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr19:1811699 G>T maps to NM_138813.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr19:1785589 G>A maps to NM_138813.2 L1091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SU-01A-31D-A391-08 chr19:1784820 G>A maps to NM_138813.2 A1219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr15:50279663 G>T maps to NM_024837.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr15:50294400 G>C maps to NM_024837.2 S152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr15:50226247 G>C maps to NM_024837.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr15:50152543 G>T maps to NM_024837.2 I1142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:50399145 C>T maps to NM_024837.2 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr15:50226327 G>A maps to NM_024837.2 Q447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr15:50211047 C>A maps to NM_024837.2 G675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr15:50152595 G>C maps to NM_024837.2 S1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr15:50158633 G>A maps to NM_024837.2 I1025I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr15:50189506 G>A maps to NM_024837.2 F893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr15:50154450 C>G maps to NM_024837.2 L1096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr15:50152601 G>C maps to NM_024837.2 S1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr15:50168657 C>A maps to NM_024837.2 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr20:50346390 G>A maps to NM_006045.1 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr20:50346462 G>T maps to NM_006045.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr20:50224072 G>A maps to NM_006045.1 I932I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr20:50273587 G>C maps to NM_006045.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr20:50305669 G>A maps to NM_006045.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr20:50290702 G>A maps to NM_006045.1 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr18:77089265 C>T maps to NM_198531.3 F633F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:47110886 A>G maps to NM_022745.3 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:17924526 G>C maps to NM_145691.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:142226808 C>T maps to NM_001184.3 K1665K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr3:142231261 T>G maps to NM_001184.3 I1564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr3:142188288 G>A maps to NM_001184.3 R2148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr3:142268452 G>A maps to NM_001184.3 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:142254047 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:142257460 C>T maps to NM_001184.3 W1196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:48505458 G>C maps to NM_130384.1 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr20:3553401 C>T maps to NM_139321.2 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr20:3571897 C>T maps to NM_139321.2 C1089C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr20:3562948 G>A maps to NM_139321.2 L904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr20:3581668 C>G maps to NM_139321.2 S1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr10:117228808 C>T maps to NM_207303.2 V1208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr10:117061383 G>A maps to NM_207303.2 A883A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr23:76854911 T>G did not map to a codon.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr23:76776903 G>C did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:76764096 C>G did not map to a codon.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr23:76939531 G>C did not map to a codon.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr23:76939542 A>G did not map to a codon.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr23:76939951 A>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:76875968 A>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:76937178 C>T did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:76931748 C>T did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:76939605 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr23:76937565 G>C did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:76937122 C>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr23:76888757 G>C did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr23:76919035 G>C did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr23:76814230 G>A did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:76938190 C>A did not map to a codon.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr23:76829714 C>G did not map to a codon.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr23:76939790 C>G did not map to a codon.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr23:76937204 G>C did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:76938031 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr23:76778780 C>G did not map to a codon.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr23:76813096 A>G did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:76938461 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr23:76856023 T>C did not map to a codon.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr23:76814246 T>G did not map to a codon.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr23:76937181 A>G did not map to a codon.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr23:76938550 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr23:76937013 G>A did not map to a codon.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr6:16328457 C>T maps to NM_000332.3 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:16327169 G>A maps to NM_000332.3 Q458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:16306793 G>C maps to NM_000332.3 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr22:46136261 G>C maps to NM_013236.3 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr22:46239024 G>A maps to NM_013236.3 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr22:46125303 G>A did not map to a codon.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr22:46098717 C>G maps to NM_013236.3 S213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr22:46114358 G>A maps to NM_013236.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:111957799 G>C maps to NM_002973.3 S450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr12:111953956 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:111890641 G>A maps to NM_002973.3 Q1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr12:111893834 G>A maps to NM_002973.3 Q1248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr12:111894030 G>T maps to NM_002973.3 L1182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr16:28847396 C>G maps to NM_148414.1 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr16:28834729 G>T maps to NM_148414.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:28847773 C>T maps to NM_148414.1 L1089L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:28845697 C>A maps to NM_148414.1 S736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr16:28840777 G>A maps to NM_148414.1 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr16:28844817 C>T maps to NM_148414.1 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr14:92548671 G>C maps to ENST00000359819 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr14:92555134 C>G maps to ENST00000359819 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr14:92537343 G>T maps to ENST00000359819 S321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr23:13337635 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:13338040 A>C did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr23:13337354 A>C did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:13337762 A>T did not map to a codon.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr3:63985135 G>A maps to NM_001177387.1 T913T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:63938122 C>T maps to NM_001177387.1 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr7:105401856 C>T maps to NM_152749.3 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr1:110029716 G>C maps to NM_153340.4 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr1:110032749 G>A maps to NM_153340.4 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr1:110031539 G>A maps to NM_153340.4 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:42274333 G>A maps to NM_020218.1 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr2:74755966 G>A maps to ENST00000258081 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:74756538 C>T maps to ENST00000258081 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr2:74754084 T>C maps to ENST00000258081 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr2:74756362 G>A maps to ENST00000258081 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:1309675 T>A maps to NM_001127230.1 K68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:8108194 G>A maps to NM_004217.2 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:57743409 C>T maps to NM_001015878.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:57746783 G>C maps to NM_001015878.1 *310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr7:70255738 C>T maps to NM_015570.2 L1179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr7:70255157 C>A maps to NM_015570.2 R986R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr7:70255357 C>T maps to NM_015570.2 I1052I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr7:70255919 C>T maps to NM_015570.2 L1240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr7:70236587 C>T maps to NM_015570.2 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr7:70227935 G>T maps to NM_015570.2 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr7:70228013 C>T maps to NM_015570.2 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr15:34163171 G>C maps to NM_020371.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr15:34159806 G>A maps to NM_020371.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:58204309 G>A maps to NM_006576.3 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr12:58191714 G>A maps to NM_006576.3 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr12:58200271 G>A maps to NM_006576.3 L514L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-A1A6-01A-11D-A13W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr7:32598685 A>G maps to NM_015060.1 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:63543728 G>A maps to NM_000706.3 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:63544138 G>A maps to NM_000706.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:206225009 C>T maps to NM_000707.3 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr1:206225297 C>T maps to NM_000707.3 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:206224502 T>C maps to NM_000707.3 N21N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr23:153171889 G>C did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr23:153172075 G>A did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr23:153171750 C>T did not map to a codon.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr23:153171631 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr23:153172087 G>T did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr23:69459701 C>G did not map to a codon.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr23:69262997 A>T did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr16:347182 C>A maps to NM_003502.3 E610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr17:63532492 G>A maps to NM_004655.3 Q696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr17:63537675 C>G did not map to a codon.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr17:63533000 C>T maps to NM_004655.3 K631K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr17:63554210 G>A maps to NM_004655.3 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:41748803 T>G maps to NM_021913.3 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr19:41737166 G>C maps to NM_021913.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr7:99569552 G>C maps to NM_001185.3 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMJ-01A-11D-A42E-08 chr7:99565997 G>A maps to NM_001185.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr17:79168757 G>C maps to ENST00000269392 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr17:79170545 C>T maps to ENST00000269392 E621E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr17:79164796 C>G maps to ENST00000269392 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr17:79165120 C>T maps to ENST00000269392 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:79170816 C>A maps to ENST00000269392 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr17:79173589 G>A maps to ENST00000269392 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr17:79164774 C>A maps to ENST00000269392 E962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr17:79176111 G>C maps to ENST00000269392 S239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr3:28379433 G>A maps to NM_022461.3 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:28381982 G>A maps to NM_022461.3 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:28382065 C>A maps to NM_022461.3 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr3:28382028 G>C maps to NM_022461.3 S27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:28378242 C>T maps to NM_022461.3 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr8:103851003 C>T maps to NM_148174.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:829703 C>T maps to NM_001700.3 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:831822 C>A maps to NM_001700.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:831822 C>G maps to NM_001700.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:829603 G>A maps to NM_001700.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr15:45003773 C>G maps to NM_004048.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr3:160803732 G>A maps to NM_033168.2 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:235618980 C>G maps to ENST00000366599 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:168725896 C>T maps to NM_020981.3 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:193150662 G>A maps to NM_003783.3 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:33245679 G>T maps to NM_003782.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:33245447 G>C maps to NM_003782.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr6:33245983 C>A maps to NM_003782.3 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr6:33246331 G>A maps to NM_003782.3 *379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:33246104 C>T maps to NM_003782.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:134252639 G>A maps to NM_054025.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr11:134257514 G>A maps to NM_054025.2 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr6:71665844 C>T maps to NM_080742.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr6:71603971 G>T maps to NM_080742.2 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr11:62389401 C>T maps to NM_012200.2 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr11:66114947 C>G maps to NM_006876.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:66114590 C>T maps to NM_006876.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:62450305 G>C maps to NM_006577.5 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr2:62449633 G>C maps to NM_006577.5 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr2:62450251 C>G maps to NM_006577.5 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr19:17919111 G>T maps to NM_014256.3 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr19:17922738 G>T maps to NM_014256.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:17918756 G>A maps to NM_014256.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:76751038 G>A maps to ENST00000354301 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr11:76751659 A>G maps to ENST00000354301 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr11:76750706 C>A maps to ENST00000354301 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr2:232262645 G>A maps to NM_145236.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:232262624 G>A maps to NM_145236.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:81006649 G>C maps to NM_001009905.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:58021629 C>T maps to NM_001478.3 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr12:58024989 G>A maps to NM_001478.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr12:58022861 C>A maps to NM_001478.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr12:58020595 G>A maps to NM_001478.3 D511D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr17:47241448 G>C did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr12:667230 C>T maps to NM_173593.3 Q862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:644425 G>A maps to NM_173593.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:569631 C>A maps to NM_173593.3 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr12:665976 C>A maps to NM_173593.3 C775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr12:670541 C>T maps to NM_173593.3 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:667786 G>A maps to NM_173593.3 V907V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:376346 G>A maps to NM_178537.4 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr11:375483 G>C maps to NM_178537.4 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr1:44451006 G>C maps to ENST00000309519 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:44450628 C>T maps to ENST00000309519 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:161143459 C>G maps to NM_003779.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:161143734 G>T maps to NM_003779.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr1:161143712 G>A maps to NM_003779.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr3:118942987 C>T maps to NM_212543.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr3:118931410 G>A maps to NM_212543.1 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:118948787 C>T maps to NM_212543.1 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr20:48256252 G>A maps to NM_004776.3 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr5:177036641 C>G maps to NM_007255.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr5:177031245 C>T maps to NM_007255.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr5:177031539 C>T maps to NM_007255.2 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr9:104124823 C>T maps to NM_001701.3 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr11:117164661 G>C maps to NM_012104.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr11:117162451 G>C maps to NM_012104.3 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr21:42629233 C>T maps to NM_012105.3 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr21:30699116 T>G maps to NM_206866.1 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr6:90642372 G>A maps to NM_001170794.1 C760C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr6:90647889 C>T maps to NM_001170794.1 Q672Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr6:90660531 C>T maps to NM_001170794.1 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr6:90660231 G>A maps to NM_001170794.1 D531D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:33264453 C>T maps to NM_004323.5 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:121431903 C>T maps to NM_004281.3 N215N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr8:38065105 C>G maps to NM_004874.2 S152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:104026369 C>A maps to NM_001015049.2 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr14:104026652 G>C maps to NM_001015049.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr21:11058165 T>A maps to NM_182482.2 K92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:79419757 G>A maps to ENST00000436173 E1442E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:79426095 C>A maps to ENST00000436173 I1874I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr17:79423487 C>T maps to ENST00000436173 L1579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr15:40751713 C>T maps to NM_014952.3 Q351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr15:40751933 C>G maps to NM_014952.3 S424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr15:40751397 G>A maps to NM_014952.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr15:40751683 G>T maps to NM_014952.3 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr15:40756199 C>G maps to NM_014952.3 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr8:143570747 G>A maps to NM_001702.2 P860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr8:143599521 G>A maps to NM_001702.2 P947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr8:143603351 C>T maps to NM_001702.2 F1017F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr8:143556840 G>A maps to NM_001702.2 W264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr8:143570757 C>T maps to NM_001702.2 L864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr8:143614662 C>T maps to NM_001702.2 L1136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:32196970 T>C maps to NM_001703.2 T1270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:32205613 G>A maps to NM_001703.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:32205545 C>T maps to NM_001703.2 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr1:32204222 C>T maps to NM_001703.2 T870T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr1:32198144 C>A maps to NM_001703.2 S1231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr6:70098734 G>C maps to NM_001704.2 L1507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:69949066 C>T maps to NM_001704.2 I921I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr6:70037751 C>T maps to NM_001704.2 T1002T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr6:69728360 C>T maps to NM_001704.2 Q693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr17:79060253 G>A maps to NM_017451.2 K121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr17:79078327 C>T maps to NM_017451.2 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr7:97944885 C>T maps to NM_018842.4 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr7:97949588 G>T maps to NM_018842.4 S79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr7:97944888 G>T maps to NM_018842.4 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr16:1398201 C>T maps to NM_003933.4 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr6:33543645 G>A maps to ENST00000360661 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:28970346 C>T maps to NM_012342.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr4:102751142 G>A maps to NM_017935.4 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:102981530 G>C maps to NM_017935.4 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:102946406 G>A maps to NM_017935.4 Q445Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr16:88017670 C>T maps to NM_001173542.1 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr16:88052190 G>A maps to NM_001173543.1 E263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr16:88105748 C>G maps to NM_001173543.1 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr16:88098938 G>T did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr16:88110194 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr3:52437910 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr3:52439897 G>A maps to NM_004656.2 Q272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:52437804 G>C maps to NM_004656.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:52437314 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr3:52441220 C>T maps to NM_004656.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:52436886 C>A maps to NM_004656.2 E631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:135458597 A>G maps to NM_020064.3 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:91182552 G>C maps to NM_020063.1 S67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:91178153 C>A maps to NM_020063.1 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:96714548 G>C maps to NM_021570.3 S221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:129246022 C>G maps to NM_003658.4 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr11:129246022 C>G maps to NM_003658.4 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr5:17275492 G>A maps to NM_006317.3 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr5:17275798 C>T maps to NM_006317.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr6:31498939 G>A maps to ENST00000417556 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr6:31500658 C>T maps to ENST00000417556 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr6:31597422 G>A maps to NM_080686.2 V685V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr6:31601374 G>A maps to NM_080686.2 R1513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr6:31590589 T>C maps to NM_080686.2 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr6:31600589 G>A maps to NM_080686.2 L1380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:134308164 C>T maps to NM_013318.3 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:134349000 C>T maps to NM_013318.3 I738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr9:134312045 G>A maps to NM_013318.3 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr9:134351454 C>T maps to NM_013318.3 F1313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr9:134363329 G>A maps to NM_013318.3 A2024A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr9:134360137 C>G maps to NM_013318.3 L1842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr1:171484972 A>G maps to ENST00000392078 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr1:171556228 C>T maps to ENST00000392078 Q2613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:171506531 G>A maps to ENST00000392078 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr6:31608052 G>A maps to ENST00000404765 Q1057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:31609348 G>A maps to ENST00000404765 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr6:31616999 G>A maps to ENST00000404765 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr6:31607378 C>G maps to ENST00000404765 V1097V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr6:31631702 C>A maps to NM_033177.3 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:31656524 G>A maps to ENST00000375842 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr6:31655464 G>T maps to ENST00000375842 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr6:31656057 G>A maps to ENST00000375842 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr6:31657388 G>A maps to ENST00000375842 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr6:31657894 G>T maps to ENST00000375842 S349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr14:76012935 G>T maps to NM_006399.3 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:49458851 C>T maps to NM_138761.3 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:49464128 C>T maps to NM_138761.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:49464255 C>T maps to NM_004324.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr14:35331266 A>T maps to NM_013448.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr14:35227930 C>T maps to NM_013448.2 L1455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr14:35253089 C>T maps to NM_013448.2 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr14:35243627 G>A maps to NM_013448.2 Q968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr7:72865288 G>A maps to NM_032408.3 I1156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr7:72873955 A>G maps to NM_032408.3 A1114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr7:72883943 G>A maps to NM_032408.3 F923F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr7:72892758 C>T maps to NM_032408.3 K344K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr7:72891239 G>A maps to NM_032408.3 Q851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr12:56996517 C>A maps to NM_013449.3 E1137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr12:56995426 G>C maps to NM_013449.3 S1327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr12:57007799 G>A maps to NM_013449.3 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr12:57009071 G>C maps to NM_013449.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr12:56998907 G>A maps to NM_013449.3 V901V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr12:56996629 G>A maps to NM_013449.3 F1099F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr12:56994882 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr12:56994859 C>T maps to NM_013449.3 W1441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr2:160245981 C>T maps to NM_013450.2 L1030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:160257123 G>A maps to NM_013450.2 Q962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr2:160287551 C>T maps to NM_013450.2 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr2:160295022 G>A maps to NM_013450.2 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr2:160205273 G>A maps to NM_013450.2 L1736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr2:160310285 G>A maps to NM_013450.2 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr2:160289268 T>C maps to NM_013450.2 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:27077156 G>A maps to NM_003986.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr11:27077156 G>C maps to NM_003986.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr11:66278498 G>A maps to NM_024649.4 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr11:66297374 G>A maps to NM_024649.4 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr12:76740244 G>C maps to NM_024685.3 S507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr12:76740825 C>T maps to NM_024685.3 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr12:76742021 C>T maps to NM_024685.3 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr4:123663256 C>T maps to NM_152618.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr16:56518756 C>T maps to NM_031885.3 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr15:73007668 C>G maps to NM_033028.3 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr15:73007722 C>T maps to NM_033028.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr15:73029817 G>T did not map to a codon.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr2:170343603 A>G maps to ENST00000419050 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr2:170343585 C>T maps to ENST00000419050 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:122760800 T>C maps to NM_176824.1 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr4:122766712 G>A maps to NM_176824.1 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr4:122780305 G>A maps to NM_176824.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:33384190 A>T did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:33392469 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr7:33423320 C>T maps to NM_198428.2 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr7:33217180 T>C maps to NM_198428.2 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:33545227 C>T maps to NM_198428.2 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr3:107520008 A>G maps to NM_001142568.1 K873K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-A3WW-01A-22D-A23M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr3:107447785 C>T maps to NM_001142568.1 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr3:107474513 C>T maps to NM_001142568.1 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:156617354 G>A maps to NM_021948.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:156622476 C>T maps to NM_021948.3 R579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr1:156621323 C>T maps to NM_021948.3 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr7:107253834 G>A maps to NM_001008405.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr7:107258965 G>A maps to NM_001008405.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr7:107253855 G>C maps to NM_001008405.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr7:107221228 A>G maps to NM_001008405.2 Q4Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:152981030 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr16:75276877 G>A maps to NM_001170714.1 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr16:75276442 C>G maps to NM_001170714.1 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr16:75276373 C>T maps to NM_001170714.1 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:94033312 G>A maps to NM_003567.2 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:94048274 G>A maps to NM_003567.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:94048274 G>A maps to NM_003567.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr1:94048112 G>A maps to NM_003567.2 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr1:94140408 G>A maps to NM_003567.2 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:94033345 G>A maps to NM_003567.2 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:94140384 G>T maps to NM_003567.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:94048269 G>C maps to NM_003567.2 S425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr20:52645062 G>A maps to NM_003657.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr1:115118215 G>T maps to NM_005872.2 Y138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:59067591 G>A maps to ENST00000407086 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:59115248 G>C did not map to a codon.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr17:59469467 C>T maps to ENST00000407086 F960F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr17:59001862 T>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr12:25002809 G>C maps to NM_001178093.1 S207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr12:25047230 G>C maps to NM_001178093.1 S98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr19:49309788 G>C maps to NM_001190.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:127512233 T>C maps to NM_016567.3 D36D. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-ZF-A9R9-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr12:50232585 G>A maps to NM_181708.2 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr12:50236696 G>A maps to NM_181708.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr3:165548515 T>A maps to NM_000055.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr3:165547567 A>C maps to NM_000055.2 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr19:41916675 C>G maps to NM_000709.3 V81V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-E7-A7XN-01A-11D-A34U-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:41925046 G>A maps to NM_000709.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr19:41928201 C>T maps to NM_000709.3 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:41916633 C>T maps to NM_000709.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr19:41916675 C>G maps to NM_000709.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr16:31122480 C>T maps to NM_005881.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr16:31122037 T>C maps to NM_005881.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr16:31122699 C>T maps to NM_005881.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:60688924 G>C maps to NM_022893.3 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr2:60688291 G>A maps to NM_022893.3 C585C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:60688204 C>G maps to NM_022893.3 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:60688969 G>T maps to NM_022893.3 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr2:60688738 G>C maps to NM_022893.3 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr14:99641423 C>T maps to NM_138576.2 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr14:99640541 G>A maps to NM_138576.2 H877H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr14:99723961 C>T maps to NM_138576.2 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr14:99641435 C>T maps to NM_138576.2 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr18:60985641 G>A maps to NM_000633.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:30309931 C>T maps to NM_138578.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:52402097 G>A maps to NM_020396.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr15:52404620 C>T maps to NM_020396.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr2:111907665 G>A maps to NM_138621.3 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr22:18171755 C>T maps to NM_015367.2 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr22:18210131 G>A maps to NM_015367.2 E430E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr22:18210207 G>T maps to NM_015367.2 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr22:18210179 C>T maps to NM_015367.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr22:18209912 A>G maps to NM_015367.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:12247764 C>G maps to NM_138722.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:45262793 C>T maps to NM_005178.4 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:187446845 G>A maps to NM_001706.4 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:187444624 C>T maps to NM_001706.4 K534K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:6930282 G>C maps to NM_181844.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:147092561 G>A maps to NM_004326.2 T867T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:147091377 C>T maps to NM_004326.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr1:147092747 G>A maps to NM_004326.2 P929P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:147095709 C>T maps to NM_004326.2 L1077L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:147086362 C>T maps to NM_004326.2 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr11:118772230 C>A maps to NM_182557.2 E741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr11:118772177 C>T maps to NM_182557.2 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr6:136599222 G>A maps to NM_014739.2 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr6:136600972 G>C maps to NM_014739.2 S11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr6:136582525 G>A maps to NM_014739.2 F878F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr6:136600966 G>T maps to NM_014739.2 S13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr6:136597081 G>A maps to NM_014739.2 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SU-01A-31D-A391-08 chr6:136594242 C>T maps to NM_014739.2 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:136596745 A>T maps to NM_014739.2 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr6:136594322 G>A maps to NM_014739.2 Q619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr11:112084476 C>T maps to NM_031938.4 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr23:39934051 C>T did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:39931886 A>G did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:39933286 C>T did not map to a codon.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr23:39933137 T>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:39931908 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr23:39930939 C>T did not map to a codon.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr23:39923134 C>G did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr23:39914663 G>A did not map to a codon.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr23:39911435 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr23:39930339 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:39933150 G>A did not map to a codon.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr23:39933315 T>C did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:39933786 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:39923193 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:39932602 T>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr23:39922006 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr23:39913223 C>T did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:129185833 G>A did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr23:129150053 G>T did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:129149013 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr23:129149757 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:129148661 G>A did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:129149534 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr23:129149372 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr23:129149589 C>T did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:129147287 A>G did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr23:129148371 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:129147376 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:129148342 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:129148343 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:129148471 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:129148877 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:129149268 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:129149513 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:129150098 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr23:129147489 C>G did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:129147470 T>C did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:129150107 G>T did not map to a codon.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr22:23603180 C>G maps to NM_004327.3 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr22:23596139 C>G maps to NM_004327.3 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr22:23626222 G>C maps to NM_004327.3 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr22:23603705 G>C maps to NM_004327.3 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr22:23523719 C>G maps to NM_004327.3 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr2:219528004 C>T maps to NM_004328.4 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:197238891 G>A maps to NM_203315.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr3:197241174 C>T maps to NM_203315.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr14:96730301 G>T maps to NM_000710.2 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr14:96707621 C>T maps to NM_000623.3 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr14:96707348 G>C maps to NM_000623.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr14:96707009 C>T maps to NM_000623.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr14:96707558 C>T maps to NM_000623.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr14:96707243 G>A maps to NM_000623.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr11:27679632 G>T maps to NM_001143810.1 S242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr11:27680120 C>T maps to NM_001143810.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr5:70786809 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:70793222 G>A maps to NM_018429.2 K642K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr5:70754467 C>G maps to NM_018429.2 S92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr5:70761988 A>G maps to NM_018429.2 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr5:70805909 T>C maps to NM_018429.2 N997N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr5:70838037 C>T maps to NM_018429.2 Q2120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:101012851 C>G maps to NM_020836.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:101005142 G>A maps to NM_020836.3 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:101005460 G>A maps to NM_020836.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr14:101004311 G>T maps to NM_020836.3 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr23:18198652 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:18234660 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:18234765 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:18209133 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr23:18209143 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:18221671 T>C did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr23:18230686 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr23:18234765 G>C did not map to a codon.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr6:56880030 G>A maps to NM_152731.2 W133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr6:56857328 C>T maps to NM_152731.2 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr10:13481366 G>A maps to ENST00000396900 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr11:61729848 C>G maps to NM_001139443.1 S348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:12866257 C>T maps to NM_017682.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr12:70070773 G>A maps to NM_032735.2 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr12:70070716 G>A maps to NM_032735.2 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:70049496 C>T maps to NM_032735.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr1:45251814 G>A maps to NM_153274.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:102317962 C>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:102317903 T>G did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr23:102471434 C>T did not map to a codon.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr16:14742409 A>T maps to NM_016561.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr16:14749054 C>T maps to NM_016561.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:14738278 C>T maps to NM_016561.2 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr20:17475185 C>A maps to NM_001195.3 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:17479525 G>A maps to NM_001195.3 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:17492695 C>T maps to NM_001195.3 Q184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr3:133118989 G>A maps to NM_003571.2 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:156212940 C>A maps to NM_199173.4 Y97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr23:152770151 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr23:152770153 G>A did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:152772349 G>C did not map to a codon.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr23:102004501 G>A did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:102004205 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:102004756 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:102004091 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:102004705 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr23:102004334 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:65494216 G>A maps to NM_152414.3 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr20:61637571 G>A maps to NM_080606.3 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr20:61637592 C>T maps to NM_080606.3 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr3:5024806 C>A maps to NM_003670.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:5025202 C>T maps to NM_003670.2 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:26277037 C>T maps to NM_030762.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr12:26276074 G>A maps to NM_030762.2 Q125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr5:78411645 C>G maps to NM_001713.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr10:60549212 G>A maps to NM_001080512.1 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr10:60553242 G>A did not map to a codon.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr10:60549575 C>T maps to NM_001080512.1 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr10:60549192 C>T maps to NM_001080512.1 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr12:32480489 G>A maps to NM_001714.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr12:32480822 G>A maps to NM_001714.2 E478E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:95482794 G>C maps to NM_001003800.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr9:95477534 G>A maps to NM_001003800.1 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:95480167 G>A maps to NM_001003800.1 T723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:95482794 G>A maps to NM_001003800.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr9:95480951 G>A maps to NM_001003800.1 Q659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr9:95484997 C>T maps to NM_001003800.1 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr9:95482947 G>T maps to NM_001003800.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr9:95477525 G>A maps to NM_001003800.1 H826H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:95477684 G>A maps to NM_001003800.1 D773D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr22:18220833 C>T maps to NM_197966.1 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr22:18220989 C>T maps to NM_197966.1 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:43520162 C>T maps to NM_001197.3 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr22:43524573 C>T maps to NM_001197.3 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:127834282 C>T did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:127821518 G>A maps to NM_139343.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:127825813 C>T maps to NM_139343.1 E179E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr12:51707618 G>A maps to NM_016293.2 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:51707672 C>T maps to NM_016293.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:51690923 G>A maps to NM_016293.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr12:51685657 G>C maps to NM_016293.2 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr8:22481851 G>C maps to NM_018688.4 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr8:22487502 C>T maps to NM_018688.4 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr11:102221265 C>A maps to NM_001166.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr11:102221617 G>A maps to NM_001166.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr2:32664624 G>A maps to NM_016252.3 V1227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr2:32666515 A>G maps to NM_016252.3 S1310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr2:32694655 A>G maps to NM_016252.3 E2107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:32832644 C>T maps to NM_016252.3 R4732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:32743449 C>T maps to NM_016252.3 Q3827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:32640518 G>A maps to NM_016252.3 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr2:32626344 T>C maps to NM_016252.3 D383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr2:32733131 C>T maps to NM_016252.3 L3262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr2:32692638 G>A maps to NM_016252.3 L1801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr2:32842872 G>T maps to NM_016252.3 E4826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr2:32832676 A>G maps to NM_016252.3 E4742E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:32678918 C>T maps to NM_016252.3 F1554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr2:32640935 C>G maps to NM_016252.3 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr2:32768540 G>A maps to NM_016252.3 L4175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr2:32640935 C>G maps to NM_016252.3 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr20:61870740 G>A maps to NM_139317.1 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr20:61870758 C>A maps to NM_139317.1 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr13:103492109 C>T maps to NM_017693.3 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr13:103459697 G>A maps to NM_017693.3 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr8:11415489 G>A maps to ENST00000427279 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr8:11405587 C>A maps to ENST00000427279 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr15:91341439 G>C maps to NM_000057.2 V1077V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr15:91341439 G>A maps to NM_000057.2 V1077V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr15:91312738 G>T maps to NM_000057.2 V826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:28601167 G>A maps to NM_000386.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr17:28599905 C>G maps to NM_000386.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr17:28576035 C>T maps to NM_000386.2 *456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:97964289 C>T maps to NM_013314.3 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr10:102045869 C>T maps to NM_173809.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr10:102045914 G>A maps to NM_173809.2 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr7:43830846 G>C did not map to a codon.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr19:40953898 G>C maps to NM_000713.2 S173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr19:40971568 G>A maps to NM_000713.2 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:169351513 G>T maps to NM_003666.2 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:169351298 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:40396421 G>A maps to NM_001003940.1 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr10:22616525 C>G maps to NM_005180.6 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr8:22033755 G>A maps to NM_006129.4 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr8:22035398 G>A maps to NM_006129.4 Q255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr8:22052310 C>T maps to NM_006129.4 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr8:22034629 C>T maps to NM_006129.4 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr8:22053100 G>T did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr8:22052269 C>T maps to NM_006129.4 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr2:69093614 G>A maps to NM_014482.1 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr23:50659571 G>A did not map to a codon.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr23:50659528 C>T did not map to a codon.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr23:50658917 T>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:50659450 G>C did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr20:6750883 G>A maps to NM_001200.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr20:6759459 C>T maps to NM_001200.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:79763624 G>T maps to NM_198892.1 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr4:79832994 C>T maps to NM_198892.1 V1098V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr4:79791989 C>T maps to NM_198892.1 Q429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr4:79747197 C>T maps to NM_198892.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:54418769 G>A maps to NM_130850.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr14:54417547 G>A maps to NM_130850.2 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr14:54417241 C>T maps to NM_130850.2 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:55739618 G>C maps to NM_021073.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr6:55739618 G>C maps to NM_021073.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr6:55739453 A>T maps to NM_021073.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr6:55659207 A>T maps to NM_021073.2 L234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr6:55625252 A>G did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr6:7862675 G>A maps to NM_001718.4 Q383Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:7727602 C>T maps to NM_001718.4 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:7727749 C>T maps to NM_001718.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:7727454 C>T maps to NM_001718.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr6:7861682 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr20:55840814 G>A maps to NM_001719.2 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr20:55840818 G>A maps to NM_001719.2 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:39957911 C>G maps to NM_181809.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:40229431 G>C maps to NM_001720.3 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr1:40228855 G>A maps to NM_001720.3 Q323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr7:34182955 T>A maps to NM_133468.3 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr7:34125677 G>C maps to NM_133468.3 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr7:34192803 C>T maps to NM_133468.3 C659C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:88677031 C>T maps to NM_004329.2 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr4:96036888 C>T maps to ENST00000440890 N130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr4:96051171 C>T maps to ENST00000440890 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr4:96046236 C>T maps to ENST00000440890 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:203420556 C>T maps to NM_001204.6 F723F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:203420418 C>G maps to NM_001204.6 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr2:203397423 G>A maps to NM_001204.6 E415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr2:203397312 C>G maps to NM_001204.6 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr2:203420608 C>T maps to NM_001204.6 Q741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr2:203383645 C>A maps to NM_001204.6 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr10:43292233 A>G maps to NM_014753.3 E514E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr10:43292636 G>T maps to NM_014753.3 E649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr10:43292395 G>A maps to NM_014753.3 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr10:43287215 A>C maps to NM_014753.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr10:43326462 G>A maps to NM_014753.3 K1256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr10:43292281 C>T maps to NM_014753.3 C530C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr23:15548140 C>G did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr23:15534290 G>T did not map to a codon.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr23:15574249 C>T did not map to a codon.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr23:15552334 T>A did not map to a codon.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr23:15540610 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:15540528 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr23:15526532 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:15526599 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr23:15560203 G>A did not map to a codon.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr15:83932685 C>T maps to NM_001717.3 K439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr15:83926766 G>T maps to NM_001717.3 A804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr15:83933234 C>T maps to NM_001717.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:83926592 C>T maps to NM_001717.3 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr15:83926592 C>A maps to NM_001717.3 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr9:16437455 G>A maps to NM_017637.5 Q246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:16435865 C>A maps to NM_017637.5 E776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:16436823 G>C maps to NM_017637.5 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:16436190 G>T maps to NM_017637.5 V667V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:16437198 G>T maps to NM_017637.5 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr9:16436151 C>T maps to NM_017637.5 E680E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr9:16552650 C>A maps to NM_017637.5 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr9:16437084 G>A maps to NM_017637.5 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr9:16419028 G>A maps to NM_017637.5 N1086N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr9:16419529 C>T maps to NM_017637.5 K919K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:16552749 G>A maps to NM_017637.5 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr9:16419502 C>T maps to NM_017637.5 G928G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr5:172585776 C>G maps to NM_013979.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr5:172585836 C>G maps to NM_013979.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr10:133784415 G>C maps to NM_004052.2 S114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:151015531 G>A maps to NM_138278.3 W178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr3:112998755 G>A maps to ENST00000273395 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:112969528 G>C maps to ENST00000273395 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr3:112992090 C>G maps to ENST00000273395 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMJ-01A-11D-A42E-08 chr3:113002378 C>T maps to ENST00000273395 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:173040144 C>T maps to NM_138369.2 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr4:13606162 G>C maps to NM_148894.2 T787T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr4:13602052 G>C maps to NM_148894.2 S2157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr4:13602067 G>A maps to NM_148894.2 F2152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr4:13601104 A>G maps to NM_148894.2 D2473D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr4:13603303 C>T maps to NM_148894.2 V1740V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr4:13601145 C>A maps to NM_148894.2 E2460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr4:13601434 C>T maps to NM_148894.2 L2363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr4:13605171 C>A maps to NM_148894.2 E1118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:13615285 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr4:13571643 C>T maps to NM_148894.2 A3049A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr4:13602475 G>A maps to NM_148894.2 V2016V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr2:242509573 G>A maps to NM_032515.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr2:242511722 C>T maps to NM_032515.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr2:242511734 C>A maps to NM_032515.3 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:149871750 G>T maps to NM_016074.3 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:149871698 C>T maps to NM_016074.3 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:149871617 G>A maps to NM_016074.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:3123965 C>T maps to NM_004332.2 H61H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr6:3137617 G>A maps to NM_004332.2 W185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr20:36959491 G>A maps to NM_001725.2 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr20:36937358 C>T maps to NM_001725.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr20:36937448 A>G maps to NM_001725.2 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr20:31600611 C>A maps to NM_025227.1 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr20:31625462 G>A maps to NM_174897.2 Q255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr20:31629774 G>A did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr20:31624293 G>C maps to NM_174897.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr20:31619479 C>T maps to NM_174897.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:31631104 C>T maps to NM_174897.2 Q421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr20:31619550 G>T did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr17:65942423 G>T maps to ENST00000321892 E2660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:65870931 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:65907509 C>T maps to ENST00000321892 V1296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr17:65908874 C>T maps to ENST00000321892 V1751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr17:65888044 C>T maps to ENST00000321892 I776I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr17:65907710 C>T maps to ENST00000321892 L1363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr17:65941561 G>A maps to ENST00000321892 Q2372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr17:65850818 A>G maps to ENST00000321892 E459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr17:65944343 C>T maps to ENST00000321892 F2742F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr17:65914841 G>A maps to ENST00000321892 Q1898Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr7:140449095 G>A maps to NM_004333.4 N661N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr7:140507792 C>G maps to NM_004333.4 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr7:140534444 G>A maps to NM_004333.4 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr7:140482859 T>C maps to NM_004333.4 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr7:140439746 C>A did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr7:140449172 G>A maps to NM_004333.4 Q636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr12:112082200 G>A maps to NM_006768.3 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr12:112082173 G>A maps to NM_006768.3 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr12:112082136 G>A maps to NM_006768.3 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr12:112082358 G>A maps to NM_006768.3 Q475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:41246521 C>G maps to ENST00000471181 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr17:41243706 G>A maps to ENST00000471181 Q1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:41242997 G>C maps to ENST00000471181 S1383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr17:41244537 C>A maps to ENST00000471181 E1004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr17:41215351 C>A maps to ENST00000471181 E1753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr17:41223130 C>T maps to ENST00000471181 L1622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr17:41245548 G>A maps to ENST00000471181 Q667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr13:32910967 G>T maps to NM_000059.3 E826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr13:32936816 C>T maps to NM_000059.3 Q2655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr13:32937529 C>T maps to NM_000059.3 Q2731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr13:32914960 C>T maps to NM_000059.3 Q2157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr13:32929378 T>C maps to NM_000059.3 N2463N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr13:32915106 G>T maps to NM_000059.3 V2205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:32914876 G>T maps to NM_000059.3 E2129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr13:32893372 C>G maps to NM_000059.3 S76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr13:32954178 A>C maps to NM_000059.3 P3051P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr13:32914136 C>G maps to NM_000059.3 S1882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr13:32912513 C>G maps to NM_000059.3 S1341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr13:32929099 A>G maps to NM_000059.3 K2370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr13:32945212 C>T maps to NM_000059.3 Q2870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr13:32900415 G>A maps to NM_000059.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr13:32972789 C>G maps to NM_000059.3 L3380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr13:32907258 G>A maps to NM_000059.3 Q548Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr23:154327653 G>A did not map to a codon.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr22:50187865 G>A maps to ENST00000342989 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr22:50192220 G>A maps to ENST00000342989 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr22:50216990 C>T maps to ENST00000342989 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr22:50216759 C>A maps to ENST00000342989 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr22:50217029 G>A maps to ENST00000342989 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr6:32944129 C>T maps to ENST00000395289 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr6:32947662 G>T maps to ENST00000395289 E669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr6:32944515 C>T maps to ENST00000395289 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:32945995 C>A maps to ENST00000395289 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr6:32944709 C>G maps to ENST00000395289 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr6:32942328 T>C maps to ENST00000395289 Y40Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr9:136918413 G>C maps to NM_007371.3 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr9:136918566 C>T maps to NM_007371.3 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr9:136917463 G>A maps to NM_007371.3 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr9:136915675 G>A maps to NM_007371.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr9:136918506 C>T maps to NM_007371.3 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:15355562 C>T maps to NM_058243.2 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr19:15366962 C>A maps to NM_058243.2 E555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr19:15349898 C>T maps to NM_058243.2 E1251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr19:15376404 C>T maps to NM_058243.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr19:15366360 C>T maps to NM_058243.2 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr16:50402639 C>A maps to NM_001173984.2 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:50383963 G>A maps to NM_001173984.2 N187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr16:50354234 C>T maps to NM_001173984.2 Q561Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr16:50354576 C>A maps to NM_001173984.2 E538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:137485476 G>A maps to NM_139199.1 Q1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr5:137499814 C>T maps to NM_139199.1 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr5:137499822 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr5:887496 T>A maps to NM_001009877.2 A179A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-XF-A9T6-01A-11D-A42E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr5:887505 G>A maps to NM_001009877.2 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:92433809 C>A maps to ENST00000347608 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:92442824 G>T maps to ENST00000347608 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:92470767 C>G maps to ENST00000347608 S908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr1:92479789 C>T maps to ENST00000347608 Q947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr2:28467645 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:28152707 A>G maps to NM_004899.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr2:28248114 C>G maps to NM_004899.3 S108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:28248193 G>A maps to NM_004899.3 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:28268590 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr2:28561341 C>T maps to NM_199191.1 Q372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr14:105685545 G>C maps to NM_001519.2 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr14:105739115 C>T maps to NM_001519.2 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr8:37706158 G>A maps to NM_018310.3 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr12:125478518 C>T maps to NM_080626.5 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr17:59853900 G>C maps to NM_032043.2 S653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr17:59761239 G>C maps to NM_032043.2 S1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr17:59763272 G>A maps to NM_032043.2 V943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr17:59821937 T>C maps to NM_032043.2 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr17:59876558 C>T maps to NM_032043.2 Q414Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:34924953 C>T maps to NM_018321.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:66108685 G>A maps to NM_001024957.1 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr11:66108728 C>T maps to NM_001024957.1 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:9776367 C>A maps to NM_001003694.1 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr3:9785586 T>C did not map to a codon.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr3:9783110 C>G maps to NM_001003694.1 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr3:9781195 T>A maps to NM_001003694.1 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr6:36168657 C>T maps to NM_015695.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr6:36168332 G>A maps to NM_015695.2 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:36178225 C>T maps to NM_015695.2 I700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr6:36168215 G>A maps to NM_015695.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr6:36169310 C>T maps to NM_015695.2 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr23:135570695 C>A did not map to a codon.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr23:135574234 T>G did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr23:135570660 T>C did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:135572430 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:135570546 G>A did not map to a codon.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr19:55816211 C>A maps to NM_032430.1 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr19:55816953 G>C maps to NM_032430.1 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:55814063 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr19:55798409 C>T maps to NM_032430.1 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr11:1463776 C>T maps to NM_003957.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr21:40568277 C>T maps to NM_033656.2 T2239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr21:40604197 G>A maps to NM_018963.3 R969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr21:40574386 C>T maps to NM_018963.3 R1483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr21:40665769 G>C maps to NM_018963.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr21:40667667 C>G did not map to a codon.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr23:79984386 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:79932200 C>G did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr23:79932316 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr23:79973159 C>A did not map to a codon.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr23:79951410 C>T did not map to a codon.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr23:79962977 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr23:79936979 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr23:79932820 C>G did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:79938034 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr23:79971670 A>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr3:49690243 G>A maps to NM_003458.3 R1085R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:49691050 C>G maps to NM_003458.3 L1354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr3:49698131 G>T maps to NM_003458.3 E2952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr3:49692494 G>T maps to NM_003458.3 E1836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr3:49695502 G>A maps to NM_003458.3 T2838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr3:49691206 C>T maps to NM_003458.3 S1406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:116131968 G>A maps to NM_017688.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:15720598 C>T maps to ENST00000382346 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:122848502 C>A maps to NM_001098169.1 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr10:93749113 C>T maps to NM_003972.2 I877I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr10:93751912 C>A maps to NM_003972.2 V964V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr10:93726463 C>T maps to NM_003972.2 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr10:93778678 C>G maps to NM_003972.2 S1617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr15:83710669 G>C maps to NM_025238.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:13435140 C>T maps to NM_032320.5 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr12:108008936 C>T maps to NM_001018072.1 Q667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr12:107937751 C>G maps to NM_001018072.1 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr12:108011967 G>A maps to NM_001018072.1 E755E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr12:108006636 G>C maps to NM_001018072.1 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:108051473 T>C maps to NM_001018072.1 S1098S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr12:107914402 C>T maps to NM_001018072.1 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr16:3640179 G>C maps to NM_032444.2 L1153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:3640392 C>T maps to NM_032444.2 Q1082Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:3632360 C>T maps to NM_032444.2 K1829K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr16:3632495 C>T maps to NM_032444.2 E1784E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:3658760 C>A maps to NM_032444.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:3658956 C>G maps to NM_032444.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:3632492 C>A maps to NM_032444.2 L1785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr16:3639471 C>T maps to NM_032444.2 A1389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:3632617 G>A maps to NM_032444.2 Q1744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr10:124036415 G>C maps to ENST00000368994 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr10:124036304 G>A maps to ENST00000368994 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr10:124096175 C>T maps to ENST00000368994 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:124036415 G>A maps to ENST00000368994 L44L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BT-A2LB-01A-11D-A18F-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BT-A3PJ-01A-21D-A21Z-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:72353374 C>T maps to ENST00000440684 Q621*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-GU-A42P-01A-11D-A23U-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-K4-A54R-01A-11D-A26M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:72353676 C>A maps to NM_001080466.1 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr19:2015431 C>A maps to NM_017797.3 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr19:1986489 G>C maps to NM_017797.3 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr20:11904178 C>G maps to NM_014962.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr14:105716180 C>T maps to NM_033271.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr14:93709010 C>A maps to NM_001002860.2 E1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr1:92613274 G>T maps to NM_183242.3 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr1:92613276 G>A maps to NM_183242.3 E352E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr1:92568028 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:38548140 A>C maps to NM_052893.1 L296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr6:38142835 C>T maps to NM_052893.1 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr3:15683503 G>A maps to NM_000060.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr3:15683561 G>T maps to NM_000060.2 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:72798794 C>T maps to NM_001037637.1 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr12:92539263 G>A maps to NM_001731.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:92537909 G>A maps to NM_001731.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:203276388 G>C maps to NM_006763.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr21:18977217 C>A maps to NM_001130914.1 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr23:100617586 T>G did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr23:100608276 C>T did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:100617171 C>T did not map to a codon.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr23:100611773 C>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:100608330 T>A did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:100611192 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:112185018 G>C maps to NM_181780.3 S269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:26501555 C>T maps to NM_001732.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:26508196 C>T maps to NM_001732.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr6:26507019 C>T maps to NM_001732.2 N273N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:26502043 C>T maps to NM_001732.2 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:26502085 C>T maps to NM_001732.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:26507020 G>T maps to NM_001732.2 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:26459742 C>T maps to NM_007049.3 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:26468644 G>A maps to NM_007049.3 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr6:26384102 C>G maps to NM_001197237.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr6:26390935 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr6:26384102 C>G maps to NM_001197237.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr6:26407947 G>T maps to NM_007048.5 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:26411781 G>A did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr6:26413832 C>T maps to NM_007048.5 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr6:26409782 G>A maps to NM_007048.5 Q246Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr6:26405877 T>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:26368409 G>C did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr6:26370778 C>T maps to NM_001197246.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr6:26370722 G>T maps to NM_001197246.1 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr6:26452305 C>T maps to NM_006994.4 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr6:26451933 C>T maps to NM_006994.4 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr6:26452380 C>T maps to NM_006994.4 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr6:26452218 C>T maps to NM_006994.4 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:26443855 C>A maps to NM_006994.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr6:26448521 G>C maps to NM_006994.4 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:26443837 C>T maps to NM_006994.4 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr6:32362584 G>A maps to ENST00000468270 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:32363974 C>A maps to ENST00000468270 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr6:32374846 G>A maps to ENST00000468270 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr5:180430854 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr5:180432733 C>T maps to NM_197975.2 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr5:180326336 G>C maps to NM_001040462.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr5:180486729 C>T maps to NM_152547.4 D492D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr10:103281472 G>A maps to NM_033637.2 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr10:103294606 C>T maps to NM_033637.2 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:111399042 T>C did not map to a codon.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr2:111427075 G>C maps to NM_004336.3 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:111425145 C>A maps to NM_004336.3 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:111427112 G>A maps to NM_004336.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr2:111408234 A>G maps to NM_004336.3 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr2:111425131 C>T maps to NM_004336.3 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:111395636 C>T maps to NM_004336.3 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr15:40502315 G>T maps to ENST00000412359 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:40512773 T>C maps to ENST00000412359 D1003D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr15:40505658 C>T maps to ENST00000412359 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr15:40512950 C>A maps to ENST00000412359 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr10:124915209 C>T maps to NM_004725.3 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:116640939 T>C did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr11:116633685 G>A maps to NM_032725.3 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr11:116633512 G>A maps to NM_032725.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:105577270 A>G maps to NM_007073.4 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr6:105548987 T>C maps to NM_007073.4 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr17:56395742 G>A maps to NM_004758.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr17:56389781 G>C maps to NM_004758.2 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr17:56397903 C>T maps to NM_004758.2 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr17:56405206 A>G maps to NM_004758.2 H25H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:56405155 G>A maps to NM_004758.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr17:56400101 G>T maps to NM_004758.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr17:56385245 C>T maps to NM_004758.2 Q1596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr17:56400388 C>G maps to NM_004758.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr17:56386651 C>T maps to NM_004758.2 K1327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr17:56390075 G>C maps to NM_004758.2 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr17:56400351 C>A maps to NM_004758.2 E385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr17:56388553 G>C maps to NM_004758.2 P1034P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr2:201677974 C>A maps to ENST00000452790 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr7:16745683 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr10:45472911 G>A maps to NM_007021.3 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr10:77818511 G>T maps to NM_032024.3 G135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr10:77818422 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:21414798 C>A maps to NM_001010896.2 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:115922907 A>G maps to NM_018017.2 N40N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr10:115895666 T>G maps to NM_018017.2 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7N-01A-11D-A391-08 chr10:98742416 G>T maps to NM_015652.2 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:98743698 C>A maps to NM_015652.2 S851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:98744269 C>T maps to NM_015652.2 I1041I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr10:124457656 C>T maps to NM_001010912.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:50374938 C>G maps to ENST00000374148 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr10:96971706 G>C maps to NM_207321.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr10:96971670 G>A maps to NM_207321.2 W264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:127429113 G>A maps to ENST00000356792 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:127434456 G>A maps to ENST00000356792 L924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr10:21804749 C>A maps to NM_207371.3 E668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr10:21804177 A>T maps to NM_207371.3 I858I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:21804707 G>A maps to NM_207371.3 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr10:21804374 G>A maps to NM_207371.3 Q793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr10:21806532 G>A maps to NM_207371.3 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr10:5789318 C>G maps to NM_017782.4 S1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr10:5791659 C>G maps to NM_017782.4 L2092L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr10:5788830 C>T maps to NM_017782.4 V1149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr10:5798581 C>T maps to NM_017782.4 L2205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:5789196 C>T maps to NM_017782.4 V1271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr10:5789626 C>T maps to NM_017782.4 R1415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr10:5789824 C>T maps to NM_017782.4 L1481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr10:5784257 T>C maps to NM_017782.4 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr10:5788317 C>A maps to NM_017782.4 T978T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr10:5798658 C>T maps to NM_017782.4 I2230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr10:5772736 C>T maps to NM_017782.4 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr10:102750228 C>G maps to NM_021830.4 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr10:102748437 C>T maps to NM_021830.4 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr10:45496298 C>A maps to NM_001039380.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:72539347 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7N-01A-11D-A391-08 chr10:99969181 C>T maps to ENST00000314594 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:99968561 G>T maps to ENST00000314594 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr10:99968656 A>T maps to ENST00000314594 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr10:71392811 G>A maps to ENST00000395055 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr10:120514103 C>T maps to NM_153810.4 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr10:75671769 G>A maps to NM_001001791.2 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:99349860 C>T maps to NM_001009997.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr10:23622055 G>A maps to NM_153714.2 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:33165319 G>C maps to NM_024688.2 *629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr10:33134528 C>A maps to ENST00000375025 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr10:33140843 G>A maps to ENST00000375025 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr10:33134531 G>A maps to ENST00000375025 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr10:50532110 G>A maps to NM_001135196.1 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr10:50530703 G>A maps to NM_001135196.1 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr10:50315960 G>A maps to NM_001031746.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr10:50227763 G>A maps to NM_001031746.3 H298H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:103607319 C>A maps to NM_024541.2 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr10:103783473 G>A maps to NM_024541.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr10:103649228 A>G maps to NM_024541.2 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr10:105885384 C>T maps to ENST00000336358 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:105903396 C>T maps to ENST00000389588 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr10:105942271 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:105947215 C>T maps to ENST00000389588 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr10:115534018 G>T maps to NM_182601.1 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr10:115531769 C>T maps to NM_182601.1 H192H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr10:118425185 G>C maps to ENST00000388884 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr10:120095855 C>T maps to NM_022063.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr10:120095810 C>T maps to NM_022063.2 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr10:124697642 C>T maps to NM_024942.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr10:124708191 C>T maps to NM_024942.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr10:128192996 G>A maps to NM_001004298.2 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr10:128193174 G>A maps to NM_001004298.2 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr10:128153309 G>A maps to NM_001004298.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr10:128193312 G>A maps to NM_001004298.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr10:128193147 C>T maps to NM_001004298.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr10:128193465 C>A maps to NM_001004298.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr10:134743184 C>G maps to NM_173572.3 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr10:118138845 G>A maps to NM_198515.2 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:111753252 G>T maps to NM_022761.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr11:111753252 G>C maps to NM_022761.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:8947367 G>C maps to NM_020643.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr11:8947286 C>T maps to NM_020643.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr11:8947079 C>T maps to NM_020643.2 Q378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr11:64878920 C>G maps to NM_013265.2 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr11:64875071 G>A maps to NM_013265.2 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:64876789 C>T maps to NM_013265.2 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr11:76175123 G>A maps to ENST00000393457 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr11:76169286 G>A maps to ENST00000393457 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:76255316 C>T maps to ENST00000393457 H909H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr11:76257334 C>T maps to ENST00000393457 I1257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr11:33589664 G>A maps to ENST00000389726 Q1083Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr11:33569352 G>A maps to ENST00000389726 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr11:33631369 G>T maps to ENST00000389726 G1422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr11:33628220 A>G maps to ENST00000389726 L1347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:33689529 G>T maps to ENST00000389726 E1800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr11:33612853 G>C maps to ENST00000389726 V1255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr11:33612853 G>A maps to ENST00000389726 V1255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr11:33604914 G>A maps to ENST00000389726 W1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr11:6231319 C>A maps to NM_173525.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr11:128774377 C>T maps to NM_145013.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:62437355 G>A maps to ENST00000431002 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:62437137 G>A maps to ENST00000431002 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr11:62435192 T>G maps to ENST00000431002 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:47073975 C>T maps to NM_001003677.1 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr11:47183187 G>A maps to NM_001003677.1 *338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr11:47073983 C>T maps to NM_001003677.1 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr11:47178646 G>A maps to NM_001003677.1 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr11:111156490 C>T maps to NM_198498.1 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:111946330 G>T maps to NM_018195.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr11:111953543 G>T maps to NM_018195.3 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr11:111946327 C>G maps to NM_018195.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:122805333 C>T maps to NM_024806.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr11:122795697 C>T maps to NM_024806.2 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr11:122817457 A>G maps to NM_024806.2 Q629Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:108277654 A>G maps to NM_152587.3 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr11:61254052 C>T maps to NM_145017.2 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr11:65685244 G>A maps to NM_001135635.1 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:114270824 C>A maps to NM_019021.2 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr11:36680735 A>T maps to NM_138787.2 *222C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr11:82644613 C>A maps to NM_145018.3 S745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:62439584 G>A maps to NM_001085372.2 *94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:63585730 C>T maps to NM_138471.1 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:64708118 C>G did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr11:64707137 G>A maps to NM_001037225.1 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr11:109294574 C>T maps to NM_207645.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr11:111405135 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:111405175 G>T maps to NM_207430.2 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:61545870 G>A maps to NM_001127392.1 V641V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:61545876 G>A maps to NM_001127392.1 E643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:61548503 C>T maps to NM_001127392.1 P853P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr11:61539166 C>T maps to NM_001127392.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr11:61539082 C>A maps to NM_001127392.1 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr11:61543556 C>T maps to NM_001127392.1 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr11:61547372 C>T maps to NM_001127392.1 I769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr12:27075564 T>C maps to NM_018164.2 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:27066550 C>T maps to NM_018164.2 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr12:27077407 C>A maps to NM_018164.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:27067368 G>T maps to NM_018164.2 S464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr12:91347835 G>A maps to NM_152638.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr12:91347849 C>A maps to NM_152638.2 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:91347631 A>G maps to NM_152638.2 D296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:82783596 G>T maps to NM_032230.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr12:110206720 C>T maps to NM_032829.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr12:32137162 A>T maps to NM_018169.3 K1092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr12:32136194 C>A maps to NM_018169.3 S769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:32136972 C>T maps to NM_018169.3 S1028S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:32137857 G>A maps to NM_018169.3 Q1323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr12:32137593 A>G maps to NM_018169.3 V1235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:13526176 C>T maps to ENST00000318426 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:21680067 G>C did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:21680079 G>A maps to NM_030572.2 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr12:4634669 G>A maps to NM_020374.2 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:4643349 C>T maps to NM_020374.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:4626292 C>A maps to NM_020374.2 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr12:4598987 C>T maps to NM_020374.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:4599750 G>A maps to NM_020374.2 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr12:40076784 A>G maps to NM_001031748.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr12:40076603 C>G maps to NM_001031748.2 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:49054187 C>T maps to NM_017822.3 E396E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:49075217 C>T maps to NM_017822.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr12:52470628 G>A maps to NM_021934.4 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:105388289 C>G maps to NM_152318.2 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr12:102572446 C>T maps to NM_017915.3 D361D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:102559616 C>T maps to NM_017915.3 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:102569338 A>G maps to NM_017915.3 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:102547645 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr12:102558257 C>T maps to NM_017915.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr12:117175648 G>A maps to NM_024738.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr12:4446327 T>C did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:88420328 G>T maps to NM_152589.1 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:112610475 C>G maps to NM_001109662.2 L3756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:112609067 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:112605676 G>A maps to NM_001109662.2 Q3913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr12:112666448 A>G did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:112608963 G>A maps to NM_001109662.2 P3791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:112673536 G>T maps to NM_001109662.2 L1660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr12:112696954 C>G maps to NM_001109662.2 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr12:112623238 G>A maps to NM_001109662.2 L3005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:112608209 C>T maps to NM_001109662.2 L3821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr12:112610616 C>T maps to NM_001109662.2 W3709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:112622707 G>A maps to NM_001109662.2 F3182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:112677686 G>A maps to NM_001109662.2 T1529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr12:112699227 T>C maps to NM_001109662.2 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr12:113624823 C>G maps to NM_032848.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:6806909 C>T maps to NM_153685.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr12:6806657 G>A maps to NM_153685.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr12:48880469 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr12:64664431 C>G maps to NM_001170633.1 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr12:64784272 G>A maps to NM_001170633.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr12:7053316 G>A maps to NM_138425.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:7053316 G>A maps to NM_138425.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:7054937 C>T maps to NM_138425.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:14976351 C>G maps to NM_175874.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:14975925 C>T maps to NM_175874.3 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr12:97051868 C>T maps to ENST00000342887 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:97137337 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:97158890 G>T maps to ENST00000342887 G1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:97112229 C>G maps to ENST00000342887 S670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:97114299 C>T maps to ENST00000342887 Q733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr12:80660234 G>A maps to NM_173591.3 V734V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:80658967 C>T maps to NM_173591.3 F725F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:80752116 C>T maps to NM_173591.3 Q2028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr12:64588241 G>A maps to ENST00000311915 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr12:64588248 C>T maps to ENST00000311915 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:64588245 T>C maps to ENST00000311915 K238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr12:48578219 C>G maps to NM_001013635.3 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:14959137 G>A maps to NM_001013698.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr12:27235287 A>G maps to ENST00000398815 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr12:93100661 G>A maps to NM_001037671.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr12:93100778 C>T maps to NM_001037671.3 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr12:110495087 C>A maps to NM_207435.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr12:25149237 G>A maps to NM_001101339.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr13:111973257 G>A maps to NM_152324.1 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr13:46946347 G>C maps to NM_025113.2 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:46942257 G>A maps to NM_025113.2 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:46924292 G>A maps to NM_025113.2 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:46942915 C>T maps to NM_025113.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr13:46919707 C>G maps to NM_025113.2 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr13:46946325 G>A maps to NM_025113.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr13:39603431 A>T maps to NM_025138.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr13:39588288 G>C maps to NM_025138.3 S367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr13:39587804 C>T maps to NM_025138.3 Q528Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr13:39588501 G>C maps to NM_025138.3 S296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr13:31543164 C>T maps to NM_152325.1 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr13:31543046 G>A maps to NM_152325.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr13:103419690 C>A maps to NM_138779.3 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr13:103418899 G>A maps to NM_138779.3 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr13:113086761 G>A maps to NM_145248.4 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr13:113052393 G>A maps to NM_145248.4 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr13:44455642 G>C maps to NM_153218.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr13:73309139 A>G maps to ENST00000377815 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr13:73329353 G>C maps to ENST00000377815 *620Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr13:113337633 T>C maps to NM_207440.1 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr13:113333782 C>G maps to NM_207440.1 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr13:37269506 C>T maps to NM_203451.2 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:37269424 C>A maps to NM_203451.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr13:37269310 C>T maps to NM_203451.2 D32D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:103338670 C>A maps to NM_001010977.1 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr14:76118231 C>G maps to NM_007176.3 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr14:57103285 G>A maps to NM_017799.3 V613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr14:57085376 A>G maps to NM_017799.3 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr14:57085349 C>A maps to NM_017799.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr14:57072402 T>C did not map to a codon.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr14:90744712 C>T maps to NM_017970.2 P1154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:90782923 C>T maps to NM_017970.2 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr14:90770437 C>T maps to NM_017970.2 W282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr14:50101216 C>T maps to NM_018139.2 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr14:50092274 T>A maps to NM_018139.2 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr14:57938267 C>T maps to NM_018168.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:45693437 C>T maps to NM_018353.4 R784R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr14:45693449 C>T maps to NM_018353.4 K780K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr14:45679580 A>C did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:74824669 C>G maps to NM_018228.2 S395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr14:74825045 G>C maps to NM_018228.2 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr14:74825507 C>T maps to NM_018228.2 F674F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr14:76668106 G>A maps to NM_017926.2 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:31922498 C>A maps to NM_080664.2 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr14:60581492 G>A maps to ENST00000404681 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr14:60588017 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr14:60581889 C>T maps to ENST00000404681 C356C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr14:50583165 G>A maps to NM_024558.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr14:50583006 G>T maps to NM_024558.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr14:93673292 G>A maps to NM_032490.4 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr14:93673205 C>A maps to NM_032490.4 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr14:93670127 C>G did not map to a codon.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr14:90398918 T>C maps to NM_145231.2 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr14:81259265 C>T maps to NM_152446.3 Q466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr14:81259105 G>A maps to NM_152446.3 Q520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr14:77872262 G>A maps to NM_001113475.1 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr14:77861082 G>C maps to NM_001113475.1 S324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr14:77880433 G>C maps to NM_001113475.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr14:77872353 C>T maps to NM_001113475.1 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr14:77873001 A>C maps to NM_138791.1 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:104037963 C>G maps to ENST00000445352 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr14:91681827 G>A maps to NM_001102368.1 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr14:91647671 C>T maps to NM_001102368.1 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr14:91655350 C>T maps to NM_001102368.1 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr14:77319639 C>T maps to NM_194287.2 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:77319686 C>T maps to NM_194287.2 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr14:77294697 C>T maps to NM_194287.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr14:77297719 T>A did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr14:99183485 G>T maps to NM_182560.2 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr14:76548636 G>T did not map to a codon.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr14:76548710 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr14:76548995 G>A maps to NM_052873.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:69262699 G>A maps to NM_207442.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr14:50472343 G>C maps to NM_001012706.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr14:50472403 C>T maps to NM_001012706.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr14:50559340 C>T maps to NM_001014830.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr14:104381497 C>T maps to NM_001127393.1 W27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:24772311 C>T maps to NM_174913.1 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr14:24769357 C>T maps to NM_174913.1 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr14:24773756 G>A maps to NM_174913.1 W569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:58605793 C>A maps to ENST00000438670 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr14:58604813 G>A maps to ENST00000438670 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr14:58604789 A>G maps to ENST00000438670 D447D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr14:58471825 G>A maps to ENST00000438670 L750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr14:60945039 G>A maps to NM_174978.2 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:60925415 C>A maps to NM_174978.2 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr14:60903563 C>G maps to NM_174978.2 *588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr14:77492995 G>A maps to NM_024496.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:77492254 G>C maps to NM_024496.2 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr14:77493064 C>G maps to NM_024496.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:77493964 C>T maps to NM_024496.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr14:77493964 C>T maps to NM_024496.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr14:77492328 G>A maps to NM_024496.2 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr14:74194192 C>T maps to NM_001043318.1 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr14:74206533 G>A maps to NM_001043318.1 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr14:74206570 G>A maps to NM_001043318.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr14:74196607 G>A maps to NM_001043318.1 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr14:74523873 C>T maps to NM_025057.2 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr14:74514681 C>T maps to NM_025057.2 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr14:95923533 G>A maps to NM_152592.3 Q257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr14:95942023 C>T maps to NM_152592.3 W45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr14:95884263 G>A maps to NM_152592.3 L943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr14:95905974 C>T maps to NM_152592.3 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr14:95903306 T>C maps to NM_152592.3 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr14:65031548 C>G maps to NM_172365.1 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr14:100792528 C>A maps to NM_207117.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr14:100795894 C>G maps to NM_207117.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:100795963 C>T maps to NM_207117.2 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr14:100793637 C>T maps to NM_207117.2 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr14:100795325 C>T maps to NM_207117.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr14:100795894 C>T maps to NM_207117.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr14:105461074 C>G maps to NM_174891.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr14:105452860 G>C maps to NM_174891.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:75198698 G>A maps to NM_020447.3 H74H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr15:24922846 G>A maps to NM_018958.2 Q611Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr15:24921967 C>G maps to NM_018958.2 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr15:24921415 G>A maps to NM_018958.2 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr15:40675212 G>A maps to NM_033286.3 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr15:40678671 C>T maps to NM_033286.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr15:34393974 C>T maps to NM_020154.2 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr15:76496184 C>G maps to NM_152335.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr15:76496190 C>T maps to NM_152335.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr15:93015518 G>A maps to NM_153040.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr15:49659796 A>G maps to NM_152647.2 Y373Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr15:49663591 G>A maps to NM_152647.2 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr15:49800543 A>C maps to NM_152647.2 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr15:90446522 G>A maps to ENST00000398333 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAME-01A-12D-A42E-08 chr15:90451510 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:75499995 C>G maps to NM_015492.4 S536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr15:75498409 G>A maps to NM_015492.4 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr15:90169197 G>C maps to NM_152259.3 R1836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr15:90167052 C>G maps to NM_152259.3 S1171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr15:90152169 G>A maps to NM_152259.3 K953K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:65871970 A>C maps to ENST00000420799 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:65890801 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr15:65883983 C>A maps to ENST00000420799 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr15:45723014 G>C maps to NM_197955.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr15:40627565 G>A maps to NM_207380.2 H466H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr15:40633062 G>A maps to NM_207380.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr15:40627508 T>C maps to NM_207380.2 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:39544422 A>G maps to NM_207445.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr15:39544395 G>A maps to NM_207445.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr15:34649514 G>A maps to ENST00000438749 K1092K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr15:34646668 C>G maps to ENST00000438749 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:34649343 C>T maps to ENST00000438749 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr15:34648799 G>A maps to ENST00000438749 W854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr15:34647750 C>T maps to ENST00000438749 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:34647760 C>T maps to ENST00000438749 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr15:34648552 G>T maps to ENST00000438749 E772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr15:34640692 A>G maps to ENST00000438749 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:40544647 C>T maps to NM_001039905.1 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:90784742 C>T maps to NM_001013657.2 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr15:74032575 G>A maps to NM_001039614.1 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr16:615069 G>A maps to ENST00000293874 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr16:685683 C>T maps to NM_032366.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr16:1400928 C>T maps to NM_001001410.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr16:67698963 G>A maps to NM_032140.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr16:29831038 C>A maps to NM_024516.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr16:89735692 G>C did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr16:89724677 C>T maps to NM_153025.1 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:31503345 G>A maps to NM_022744.2 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr16:2510686 C>T maps to NM_025108.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr16:2510979 C>T maps to NM_025108.2 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr16:19628105 G>A maps to NM_020314.5 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr16:19710912 C>G maps to NM_020314.5 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:19656272 T>C did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr16:19592887 C>T maps to NM_020314.5 Y273Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr16:19680551 G>A maps to NM_020314.5 K853K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr16:19653727 G>T maps to NM_020314.5 E688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr16:15961341 A>G maps to NM_144600.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr16:8728936 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:8732963 C>G maps to NM_024109.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:8729107 G>T maps to NM_024109.2 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:89777027 C>T maps to NM_004913.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr16:89774355 C>G maps to NM_004913.2 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr16:89779124 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr16:89785446 C>A maps to NM_004913.2 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr16:89776195 C>A maps to NM_004913.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr16:67181012 G>A maps to NM_025187.3 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr16:67166811 G>T maps to NM_025187.3 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr16:4790488 G>A maps to NM_139170.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr16:4790566 G>T maps to NM_139170.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr16:4797520 G>A maps to NM_139170.2 Q486Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:4797370 C>G maps to NM_139170.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr16:4790536 C>T maps to NM_139170.2 C220C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr16:9196893 C>T maps to NM_014117.2 Q121*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-E7-A97P-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr16:11444538 C>T maps to NM_152308.1 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:11444613 G>A maps to NM_152308.1 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr16:46836866 G>C maps to NM_001001436.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr16:46836884 G>A maps to NM_001001436.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr16:46836947 G>A maps to NM_001001436.2 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr16:5115732 C>T maps to ENST00000350219 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr16:5105265 T>C maps to ENST00000350219 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr16:5112507 C>G maps to ENST00000350219 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr16:1470432 T>A maps to NM_001010878.1 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr16:1470093 C>T maps to NM_001010878.1 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr16:30768823 C>T maps to NM_001014979.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr16:30770755 G>C maps to NM_001014979.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr16:30771629 G>C maps to NM_001014979.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr17:32906017 G>C maps to NM_207454.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr17:21147511 G>A maps to NM_152914.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:42745072 G>C maps to NM_001145080.2 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr17:72954436 G>A maps to NM_030630.2 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:72949732 C>T maps to NM_030630.2 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr17:72959942 G>A maps to NM_030630.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr17:72956327 G>A maps to NM_030630.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr17:37886522 C>T maps to NM_032339.3 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr17:37886528 G>A maps to NM_032339.3 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:29231287 G>A maps to NM_024683.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr17:29226578 G>A maps to NM_024683.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr17:43332859 G>C maps to NM_152343.2 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr17:43333101 G>A maps to NM_152343.2 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:43333140 G>A maps to NM_152343.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:56620914 C>T maps to NM_001038704.1 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr17:56619288 G>A maps to NM_001038704.1 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:56620719 A>C maps to NM_001038704.1 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr17:10608308 C>T maps to NM_020233.4 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr17:34091549 G>A maps to NM_145272.3 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr17:34091528 C>G maps to NM_145272.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:42232691 C>A maps to NM_024032.3 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr17:42225569 C>T maps to NM_024032.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr17:42230003 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr17:42230090 G>A maps to NM_024032.3 E465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr17:79207837 C>G maps to NM_144679.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr17:65989035 C>T maps to NM_181656.3 *76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr17:80403797 C>T maps to NM_001193657.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:54893198 G>A maps to NM_001085430.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr17:8141515 G>A maps to NM_025099.5 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr17:8141557 G>C maps to NM_025099.5 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr17:8137936 G>A maps to NM_025099.5 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:8141718 C>G maps to NM_025099.5 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:8146436 G>C maps to NM_025099.5 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr17:8132717 G>A maps to NM_025099.5 Q1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr17:8140761 C>T maps to NM_025099.5 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:79517598 C>T maps to NM_025161.5 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:79517475 G>A maps to NM_025161.5 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:79514658 C>A maps to NM_025161.5 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr17:79517865 G>A maps to NM_025161.5 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:57289101 C>T maps to NM_018149.6 Q564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:57290754 G>A maps to NM_018149.6 R857R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:7329871 G>T maps to NM_175734.4 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr17:7329762 C>T maps to NM_175734.4 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr17:7330188 C>T maps to NM_175734.4 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr17:72588298 C>G maps to NM_152460.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:71232396 C>G maps to NM_017941.4 S259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr17:71231890 G>C maps to NM_017941.4 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:71231890 G>T maps to NM_017941.4 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:7160257 C>T maps to NM_203414.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr17:7162031 G>A maps to NM_203413.1 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr17:59490090 G>A maps to NM_203425.1 *252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:74729740 C>G maps to ENST00000317409 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr18:13621233 G>A maps to NM_181481.3 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr18:13612735 G>A maps to NM_001003674.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr18:34387819 C>T maps to NM_015476.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr18:34376983 G>C maps to NM_015476.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr18:77794533 G>T maps to NM_024805.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr18:43796349 C>T maps to NM_145055.3 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr18:43796551 G>T maps to NM_145055.3 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr18:43795963 C>T maps to NM_145055.3 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr18:43820139 G>C maps to NM_145055.3 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr18:30926329 G>T maps to NM_001105528.1 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr18:30846941 C>T maps to NM_001105528.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr18:30804900 C>G did not map to a codon.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr18:30672755 G>C maps to NM_001105528.1 S786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr18:30969578 G>A maps to NM_001105528.1 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr18:30969543 G>A maps to NM_001105528.1 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr18:20936610 G>A maps to NM_032933.4 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr18:51898904 C>T maps to ENST00000382911 Q466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr18:51898936 G>A maps to ENST00000382911 K476K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr18:71816165 G>A maps to NM_014177.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr18:21084404 C>G maps to NM_013326.3 S58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr18:21106667 C>G maps to NM_013326.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr18:21083603 C>T maps to NM_013326.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr19:4668609 A>G maps to NM_019107.3 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:30199164 G>A maps to NM_001031726.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr19:30199320 C>A maps to NM_001031726.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:30199296 G>A maps to NM_001031726.2 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr19:58472792 C>T maps to NM_152474.4 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:757911 G>A maps to NM_173481.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr19:902051 G>A maps to NM_138774.3 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr19:1475147 G>T maps to ENST00000427685 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr19:1231041 C>A maps to NM_152769.2 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr19:1233482 G>A maps to ENST00000382477 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr19:3548010 C>A maps to NM_021731.2 V224V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BT-A20N-01A-11D-A14W-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BT-A42E-01A-11D-A23U-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr19:3623700 G>A maps to NM_021231.1 T209T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FD-A6TC-01A-21D-A339-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:3623859 C>T maps to NM_021231.1 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:3620191 C>A maps to NM_021231.1 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr19:2276227 G>A maps to NM_198532.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr19:2098099 C>T maps to NM_001039846.1 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:2097471 C>T maps to NM_001039846.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:11486493 C>T maps to NM_175871.3 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr19:11486190 G>A maps to NM_175871.3 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:11485451 C>G maps to NM_175871.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr19:33467383 G>A maps to NM_152266.3 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:33467473 C>T maps to NM_152266.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr19:33467500 G>C maps to NM_152266.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:33467500 G>C maps to NM_152266.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:50657921 C>T maps to NM_152358.2 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:50666220 C>A maps to NM_152358.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:16770801 C>T maps to ENST00000358726 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr19:16613996 C>G maps to NM_032207.2 S294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr19:16612136 A>G maps to NM_032207.2 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:7571013 C>G maps to NM_198534.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:7565878 G>T maps to NM_198534.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:7569022 C>T maps to NM_198534.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:7566163 C>T maps to NM_198534.2 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr19:36494328 G>A maps to ENST00000455847 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:36494239 C>T maps to ENST00000455847 *583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr19:40827845 C>T maps to ENST00000357884 Q404Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr19:40828046 C>A maps to ENST00000357884 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr19:18679353 C>T maps to NM_024069.3 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:55672074 C>T maps to ENST00000301249 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:55676783 C>T maps to ENST00000301249 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr19:55670710 C>A maps to ENST00000301249 E516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr19:55672735 G>A maps to ENST00000301249 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:11040317 G>A maps to NM_138358.2 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr19:13885490 G>T maps to NM_014047.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr19:41248514 C>T maps to NM_198476.3 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr19:41248526 G>A maps to NM_198476.3 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr19:12779428 C>T maps to NM_016145.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr19:14000222 C>G maps to ENST00000454313 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:7743013 C>G maps to NM_174918.2 S70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:18700372 C>T maps to NM_001100418.1 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:44235748 C>G maps to NM_019108.2 *521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr19:44251839 A>G maps to NM_019108.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr19:50982319 C>G maps to ENST00000376920 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr19:49622030 G>A maps to NM_018111.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr7:7278180 G>A maps to NM_020156.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr7:7278162 G>A maps to NM_020156.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr23:119760834 G>T did not map to a codon.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr23:119760537 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr23:119760154 C>G did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:22987542 C>T maps to NM_000491.3 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:22987516 C>T maps to NM_000491.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr17:5338203 C>A maps to NM_001212.3 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:43044834 G>C maps to NM_006688.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr2:119915320 C>T maps to NM_182528.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr12:49729942 G>A maps to NM_001008223.1 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr17:77043905 C>T maps to ENST00000392445 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr17:77044106 C>T maps to ENST00000392445 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr17:77043908 C>T maps to ENST00000392445 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr17:77043908 C>T maps to ENST00000392445 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr5:34043212 G>T maps to NM_181435.4 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:34033410 G>A maps to NM_181435.4 Q190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr5:34043074 G>A maps to NM_181435.4 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:47611501 G>A maps to NM_031909.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr11:47612131 G>A maps to NM_031909.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr4:15444236 T>C maps to NM_001135170.1 H235H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr4:15444374 C>A maps to NM_001135170.1 Y281*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-AA75-01A-11D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr13:24895488 G>A maps to NM_178540.3 E195E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-XF-AAN5-01A-11D-A42E-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-4Z-AA82-01A-11D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr13:24466042 G>A maps to NM_001135816.1 T108T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-A6AW-01A-11D-A30E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:7241522 G>A maps to ENST00000290575 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:7188311 G>A maps to ENST00000290575 Q562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr12:7241972 C>A maps to ENST00000290575 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:7254566 G>A maps to NM_016546.2 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:7175802 G>A maps to NM_001734.3 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr12:7177162 T>A maps to NM_001734.3 C425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr12:7173212 C>T maps to NM_001734.3 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:244541774 C>A maps to NM_001012970.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr1:244724184 C>T maps to NM_001130957.1 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:111492646 C>T maps to NM_018372.3 K565K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:111490847 G>A maps to NM_018372.3 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:200880790 C>T maps to NM_018265.2 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr1:200877930 T>G maps to NM_018265.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr1:38155471 C>T maps to NM_017850.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr1:38149078 A>G maps to NM_017850.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:38155465 C>T maps to NM_017850.1 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:162824959 G>A maps to NM_178550.4 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr1:162829298 C>T maps to NM_178550.4 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:162343918 G>A maps to NM_182581.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:169811666 T>A maps to NM_018186.2 L612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:169771853 G>A maps to NM_018186.2 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:169366569 C>T maps to ENST00000367806 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:207195451 C>A maps to NM_023938.5 E553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr1:53683875 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:231487324 C>T maps to NM_001010984.1 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr1:179414166 C>G maps to NM_144696.4 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr1:179414150 C>G maps to NM_144696.4 S537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr1:179462007 A>G maps to NM_144696.4 V770V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:11017750 C>T maps to NM_001170754.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:11008901 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:11008453 C>A maps to NM_001170754.1 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:11007720 C>T maps to NM_001170754.1 *824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:24112803 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr1:170961421 G>A maps to NM_001163629.1 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:170961385 G>A maps to NM_001163629.1 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:170959045 T>C maps to NM_001163629.1 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:170965665 G>C maps to NM_001163629.1 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr1:170914720 A>G maps to NM_001163629.1 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:170952561 G>C did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:24921939 C>T maps to NM_001010980.4 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:26163916 G>A maps to NM_024037.1 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:182921953 G>C maps to ENST00000287709 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SU-01A-31D-A391-08 chr1:16719752 C>A maps to NM_001114600.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr1:247737500 C>T maps to NM_145278.3 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:169761963 G>A maps to NM_033418.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr1:12819367 G>A maps to NM_152290.2 W117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:12820736 C>G maps to NM_152290.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:116670902 G>A maps to NM_152367.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:112019435 C>G maps to NM_174896.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:53163959 G>C maps to NM_023077.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:27277224 C>T maps to NM_152365.2 Q354Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:75055629 G>A maps to NM_001002912.4 Q621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:75038857 C>A maps to NM_001002912.4 E846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr1:75036914 C>T maps to NM_001002912.4 A1493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr1:75038413 A>G maps to NM_001002912.4 L994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:75037068 G>C maps to NM_001002912.4 S1442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:75065508 A>G maps to NM_001002912.4 D532D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:75038408 G>A maps to NM_001002912.4 S995S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:75038327 G>C maps to NM_001002912.4 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:75037874 C>T maps to NM_001002912.4 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr1:75038009 G>A maps to NM_001002912.4 N1128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:3807549 C>T maps to NM_207356.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr1:3807549 C>T maps to NM_207356.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:55136237 G>C maps to ENST00000454855 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:55161105 G>A maps to ENST00000454855 P998P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr1:55174708 G>A maps to ENST00000454855 E1259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr1:55172133 C>T maps to ENST00000454855 F1226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:55277825 G>C maps to NM_001110533.1 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr1:55282767 C>G maps to NM_001110533.1 S386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:156316676 G>A maps to NM_144627.3 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:156316656 G>T maps to NM_144627.3 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr1:112281852 C>T maps to NM_019099.4 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:206241587 C>T maps to NM_001007544.1 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:11766605 G>C maps to NM_198545.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr1:161334763 G>C maps to NM_001013625.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr1:24706211 G>T maps to ENST00000374409 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr1:24696234 C>A maps to ENST00000374409 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:184446657 C>T maps to NM_030806.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:23696056 G>A maps to ENST00000507744 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:36181307 G>A maps to NM_152374.1 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:36181316 G>A maps to NM_152374.1 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr1:213009359 C>T maps to NM_001024601.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:186368153 G>A maps to NM_017847.5 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr1:228289065 G>A maps to NM_024319.2 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr1:28206335 C>T maps to NM_001105556.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:28206494 C>T maps to NM_001105556.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:28208598 G>A maps to NM_001105556.1 W255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:28208581 G>A maps to NM_001105556.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:178483196 G>A maps to NM_032126.4 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:178491475 G>A maps to NM_032126.4 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:150259020 C>T maps to NM_144697.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:226180267 T>A maps to NM_152608.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:226180268 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:226180134 C>A maps to NM_152608.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:151021022 C>T maps to NM_017860.3 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:151020667 C>T maps to NM_017860.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:151020343 G>A maps to NM_017860.3 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr1:151020850 C>T maps to NM_017860.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr1:109191263 G>C maps to ENST00000370031 S400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:109192904 G>A maps to ENST00000370031 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:25569142 T>C maps to NM_020317.3 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:223568535 G>A maps to NM_152610.2 Q573Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr1:156703212 G>A maps to NM_015997.3 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:156698907 C>T maps to NM_015997.3 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr1:228362967 C>T maps to NM_001010867.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:153610860 C>T maps to NM_015607.2 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:54554417 G>A maps to ENST00000371331 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:43869300 C>T maps to ENST00000310739 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:156263940 C>T maps to NM_144580.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:2125481 C>T maps to ENST00000359030 L51L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FD-A3B6-01A-21D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:2125220 C>T maps to ENST00000359030 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr1:60520968 C>A maps to NM_152377.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:60505819 A>G maps to NM_152377.2 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:60463290 C>G maps to NM_152377.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:60491134 C>G maps to NM_152377.2 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr1:60476111 C>A maps to NM_152377.2 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:16559111 G>C maps to NM_030907.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:172526518 T>A maps to ENST00000367723 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:172560174 G>T maps to ENST00000367723 V1111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr1:32687560 C>T maps to NM_019118.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:156899115 G>A maps to NM_144702.2 K347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:156901817 C>T maps to NM_144702.2 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr1:2520045 C>T maps to NM_001195736.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr1:2520385 C>T maps to NM_001195736.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr6:31905100 G>T maps to ENST00000437789 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr20:9496202 G>C maps to NM_012261.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr20:61572868 A>G maps to NM_017896.2 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr20:61574869 C>T maps to NM_017896.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr20:42825949 C>T maps to NM_016470.6 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FM-01A-11D-A38G-08 chr20:35444500 C>T maps to NM_080627.2 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr20:35467774 G>A maps to NM_080627.2 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr20:35467622 G>C maps to NM_080627.2 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:18365117 G>T maps to NM_001099407.1 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:18377124 G>T maps to NM_001099407.1 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr20:18379184 T>C maps to NM_001099407.1 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr20:18429629 G>C maps to NM_001099407.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr20:35766313 G>A maps to ENST00000343811 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr20:35743656 C>T maps to ENST00000343811 Q844Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr20:35749405 G>C maps to ENST00000343811 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr20:32255545 G>A maps to NM_001024675.1 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr20:62493564 C>T maps to NM_080622.3 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr20:2796219 C>A maps to NM_080739.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr20:32251483 G>T maps to NM_080825.3 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr20:60987918 G>A maps to NM_080833.2 D571D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:60991272 C>T maps to NM_080833.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr20:60990647 G>A maps to NM_080833.2 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:34583039 G>A maps to ENST00000373973 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr20:34618458 G>A maps to ENST00000373973 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr20:34583057 G>A maps to ENST00000373973 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:34596336 C>T maps to ENST00000373973 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr20:34618443 C>T maps to ENST00000373973 C535C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr20:44515155 C>G maps to NM_080608.3 *228Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr20:61167811 G>C maps to NM_178463.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr20:58519018 G>A maps to NM_022106.2 W7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr20:58519915 G>A maps to NM_022106.2 W306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr20:58520020 C>T maps to NM_022106.2 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr20:31647767 C>G maps to NM_182658.1 S153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:31661409 G>A maps to NM_182658.1 *477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr20:31643270 C>G maps to NM_182658.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr20:31699225 T>C maps to NM_182519.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr20:31682937 A>T maps to NM_182519.2 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr20:31688260 A>G maps to NM_182519.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr20:31685466 C>A maps to NM_182519.2 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr20:31685589 C>T maps to NM_182519.2 D522D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr20:31671335 C>T maps to NM_182519.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr20:3305599 C>A maps to NM_001009984.1 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:3298956 G>A maps to NM_001009984.1 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr20:3278775 G>C maps to NM_001009984.1 S610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr20:3362092 T>C maps to NM_001009984.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr20:3233277 C>T maps to NM_001009984.1 E1158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr20:62187951 C>T maps to NM_024059.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr20:62187183 G>C maps to NM_024059.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr20:62187645 C>T maps to NM_024059.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr20:5753597 C>T maps to NM_152504.2 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr20:61428555 G>C maps to NM_018270.4 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr20:61428023 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr20:20056135 C>G maps to ENST00000389655 S148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr20:20177347 G>T maps to ENST00000389655 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:20269275 G>A maps to ENST00000389655 K943K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr20:20056135 C>G maps to ENST00000389655 S148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr20:20144788 C>A maps to ENST00000389655 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr20:20055896 C>T maps to ENST00000389655 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:20177311 C>G maps to ENST00000389655 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:20071508 C>G maps to ENST00000389655 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr20:3736236 G>A maps to NM_001039140.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr20:3804754 G>A maps to NM_018347.1 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr20:24944655 G>C maps to NM_020531.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr20:5081550 C>T maps to NM_001009923.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr20:34832692 C>T maps to NM_015511.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr20:34828020 C>T maps to NM_015511.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr20:34827930 C>T maps to NM_015511.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr20:34843606 G>A maps to NM_015511.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr20:55088465 G>A maps to ENST00000357348 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr20:1161989 G>C maps to NM_018354.1 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr20:746034 C>T maps to NM_033409.3 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr20:13765903 G>T maps to NM_024120.4 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr20:13765903 G>T maps to NM_024120.4 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr20:13775548 C>T maps to NM_024120.4 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr20:31760843 C>T maps to NM_080574.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr20:31805356 C>T maps to NM_178466.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr20:31812909 C>T maps to NM_178466.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr20:31812999 G>A maps to NM_178466.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr20:31811632 C>A maps to NM_178466.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr20:31814241 C>G maps to NM_178466.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:17950540 C>G maps to NM_052865.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr20:17950747 G>C maps to NM_052865.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr20:56728656 G>A maps to NM_178456.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:56735718 C>A maps to NM_178456.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:10541381 C>A maps to NM_001009608.1 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr20:10536901 G>A maps to NM_001009608.1 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr20:10602053 G>C maps to NM_001009608.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr20:10579380 C>T maps to NM_001009608.1 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr20:256640 G>C maps to NM_153269.1 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr20:259902 G>A maps to NM_153269.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr21:45948428 C>T maps to ENST00000443468 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr21:45950979 C>T maps to ENST00000443468 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr21:45948466 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr21:45945580 C>A maps to ENST00000443468 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr21:45947228 C>T maps to ENST00000443468 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr21:45563203 C>T maps to NM_004649.6 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr21:47588240 C>T maps to NM_001142854.1 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr21:33976578 G>A maps to NM_021254.2 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr21:33974617 C>G maps to NM_021254.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr21:30521508 G>C did not map to a codon.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr21:30464816 C>T maps to NM_020152.2 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr21:46363636 C>A maps to NM_058190.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr21:46363699 C>T maps to NM_058190.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr21:46387036 C>T maps to NM_058190.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:19169379 G>A maps to NM_001100420.1 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:24943896 G>A maps to ENST00000266155 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr22:32330183 G>A maps to NM_015372.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr22:19839451 C>T maps to NM_024627.5 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:19839387 G>A maps to NM_024627.5 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr22:19839433 G>A maps to NM_024627.5 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr22:32097733 C>T maps to NM_173566.2 K2005K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr22:32099657 C>A maps to NM_173566.2 E1960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:32108124 G>A maps to NM_173566.2 I1900I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr22:29454842 G>A maps to NM_015370.1 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr22:29454978 G>T maps to NM_015370.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr22:42475828 C>T maps to NM_033318.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr22:37398084 C>T maps to NM_001163857.1 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr22:45595790 G>A maps to NM_001009880.1 N326N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr22:45601540 C>T maps to NM_001009880.1 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr21:43334725 G>A maps to NM_015500.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr21:43309334 C>T maps to NM_015500.1 R663R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr21:43309388 G>C maps to NM_015500.1 G645G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr11:118978726 C>G maps to NM_014807.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr11:118983037 G>A maps to NM_014807.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:73849869 G>A maps to ENST00000334126 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr11:73849845 G>A maps to ENST00000334126 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:73789717 G>A maps to ENST00000334126 L1349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:99767183 G>T maps to NM_144706.2 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr2:220041502 G>A maps to NM_015680.4 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr2:220040383 G>A maps to NM_015680.4 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr2:220037643 C>T maps to NM_015680.4 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr2:27439744 C>T maps to NM_080592.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:27438517 C>G maps to NM_080592.3 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:101869620 G>A maps to NM_017546.4 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr2:75933712 C>T maps to NM_003203.4 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr2:75915022 C>T maps to NM_003203.4 K540K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:75923440 C>A maps to NM_003203.4 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr2:75907338 C>A maps to NM_003203.4 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr2:75899074 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr2:26676408 G>A maps to NM_145038.2 K637K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:26624902 G>T maps to NM_145038.2 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:26676222 G>A maps to NM_145038.2 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr2:26624884 C>T maps to NM_145038.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr2:26667761 C>T maps to NM_145038.2 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:70408761 G>C maps to NM_017880.1 S119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr2:20901368 C>T maps to ENST00000381090 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:24261332 C>G maps to NM_025203.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr2:200824490 G>A maps to NM_024520.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:200820838 G>A maps to NM_024520.2 Q106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:11280653 C>T maps to NM_182500.2 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:88828628 C>T maps to NM_152670.2 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr2:27360964 G>C maps to NM_178553.3 S78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:27360540 C>T maps to NM_178553.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:27360612 G>A maps to NM_178553.3 C195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr2:27361073 G>A maps to NM_178553.3 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr2:241831157 C>T maps to NM_001085437.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr2:99454631 G>C maps to NM_207362.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:99413947 C>T maps to NM_207362.2 A823A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr2:99439385 C>T maps to NM_207362.2 E450E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:47378468 C>T maps to NM_001163561.1 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:55407748 G>T maps to NM_152385.2 Y427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:55403042 C>T maps to NM_152385.2 Q548Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr2:99220587 C>A maps to NM_001008215.1 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr2:99224805 C>T maps to NM_001008215.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:74834256 G>A maps to NM_138804.3 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:74787418 C>G did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr2:74842182 G>A maps to NM_138804.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr2:197672316 C>T maps to NM_213608.1 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr2:197674105 G>T maps to NM_213608.1 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr2:210962865 T>G maps to NM_152519.2 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:85836115 G>C maps to NM_001013649.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr2:26802257 T>C maps to NM_001105519.1 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr2:26800451 G>A maps to NM_001105519.1 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:29295004 G>C maps to NM_001029883.1 S708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr2:29293656 C>T maps to NM_001029883.1 G1157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr2:29294895 C>G maps to NM_001029883.1 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:29294358 G>A maps to NM_001029883.1 D923D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr2:54570909 C>T maps to NM_001100396.1 Y96Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr2:120097411 G>A maps to NM_001017927.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:170506886 T>C maps to NM_001085447.1 E368E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:170502385 G>A maps to NM_001085447.1 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr2:170502422 G>C maps to NM_001085447.1 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr2:170518891 A>G maps to NM_001085447.1 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:74043854 C>T maps to NM_001080474.1 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr2:74043845 G>T maps to NM_001080474.1 V832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:74040880 C>T maps to NM_001080474.1 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:74040781 C>G maps to NM_001080474.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr2:228497735 C>T maps to NM_020161.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:242815143 C>T maps to NM_173821.2 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr2:242814594 C>T maps to NM_173821.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:63631243 G>A maps to NM_015910.4 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:63631225 G>C maps to NM_015910.4 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:85097588 G>A maps to ENST00000409520 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:85097648 G>A maps to ENST00000409520 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:85108115 G>C maps to ENST00000409520 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:85051229 G>C maps to ENST00000409520 S394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr2:85097727 G>C maps to ENST00000409520 S97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:6692952 C>T maps to NM_000064.2 V1124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr19:6707889 C>T maps to NM_000064.2 G632G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:6712593 G>T maps to NM_000064.2 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:6696438 G>C maps to NM_000064.2 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:6693442 C>G maps to NM_000064.2 V1070V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr19:6719356 C>A maps to NM_000064.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr19:6697704 G>A maps to NM_000064.2 I847I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr19:6719302 G>A maps to NM_000064.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr12:8212247 G>A maps to NM_004054.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr12:8211911 G>C maps to NM_004054.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr3:119222467 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr3:119451309 C>G maps to NM_033364.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr3:119456226 G>A maps to NM_033364.3 K453K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr3:119445048 G>A maps to NM_033364.3 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:119459478 G>A maps to NM_033364.3 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr3:119434528 A>G maps to NM_033364.3 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T4-01A-11D-A391-08 chr3:119449126 G>A maps to NM_033364.3 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr3:119434461 C>G maps to NM_033364.3 S185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr3:112732195 C>T maps to NM_015412.3 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr3:112732135 G>A maps to NM_015412.3 C152C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr3:50602917 C>G maps to NM_001171741.2 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr3:14709680 A>G maps to NM_016474.4 E315E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:14798892 G>A maps to NM_032137.4 E652E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:14724253 C>T maps to NM_032137.4 Q12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr3:14756870 G>A maps to NM_032137.4 W463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:14746119 C>T maps to NM_032137.4 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:194790761 G>A maps to NM_152531.4 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr3:194991364 G>A maps to NM_152531.4 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr3:126272146 G>A maps to NM_152533.1 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:44434459 C>G maps to NM_173826.3 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr3:10145992 G>A maps to NM_001164839.1 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr3:99885223 C>G maps to NM_032359.3 S134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr3:118865710 G>A maps to NM_152539.2 Q225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:118865407 T>C maps to NM_152539.2 N124N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr3:11851123 C>T maps to ENST00000444133 Q247Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr3:11880709 G>A maps to ENST00000444133 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr3:8675374 G>A maps to NM_015931.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr3:8675498 G>C maps to NM_015931.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr3:8667329 C>T maps to NM_015931.1 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr3:37476521 C>T maps to NM_178339.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr3:133647344 C>T maps to NM_025041.2 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr3:133647233 G>C maps to NM_025041.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:129023625 G>A maps to NM_001006109.1 E341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:129023616 G>A maps to NM_001006109.1 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:129007758 C>T maps to NM_001006109.1 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr3:129023436 C>G maps to NM_001006109.1 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr3:43122016 C>A maps to NM_032806.4 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr3:43122368 C>A maps to NM_032806.4 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:43122497 G>A maps to NM_032806.4 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:43122263 C>T maps to NM_032806.4 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:111831981 C>G maps to NM_024616.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr3:157289760 C>T maps to NM_001130002.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr3:143691455 G>C maps to NM_173552.3 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr3:143691548 C>A maps to NM_173552.3 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr3:143691542 G>A maps to NM_173552.3 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr3:192516741 G>A maps to NM_178496.3 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr3:192516516 G>A maps to NM_178496.3 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr3:192516719 G>A maps to NM_178496.3 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr3:192516175 C>T maps to NM_178496.3 *492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:49308833 C>A maps to NM_198562.2 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr3:49314170 C>T maps to NM_198562.2 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr3:49311572 C>T maps to NM_198562.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr3:56667188 G>A maps to ENST00000447900 S1210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:69027582 G>A maps to ENST00000383701 Y446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr3:69050834 G>C maps to ENST00000383701 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:69053538 G>A maps to ENST00000383701 L204L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-4Z-AA84-01A-11D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:184800808 C>A maps to NM_001025266.1 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr3:184801133 A>T maps to NM_001025266.1 C138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:47539847 G>A maps to NM_001031703.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:31997502 A>C maps to ENST00000425700 A1279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:207300064 C>T maps to NM_000715.3 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:207314559 C>T maps to NM_000715.3 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:207314611 C>T maps to NM_000715.3 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:207307812 T>G maps to NM_000715.3 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr1:207314568 G>A maps to NM_000715.3 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr1:207297547 C>T maps to NM_000715.3 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:207273240 G>T maps to NM_001017367.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr4:57842716 G>T maps to NM_032313.2 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr4:57842851 C>T maps to NM_032313.2 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr4:57829645 C>T maps to NM_032313.2 V689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr4:100458839 C>G maps to NM_032149.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr4:100451105 G>A maps to NM_032149.2 Q179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr4:113540251 G>A maps to NM_018392.4 Q316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr4:113474996 C>T maps to NM_018392.4 L1780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:113541343 C>T maps to NM_018392.4 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr4:113461039 G>A maps to NM_018392.4 R2051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr4:81256998 C>A maps to ENST00000508675 S26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr4:8456476 C>A maps to NM_152544.2 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr4:128938604 G>A maps to ENST00000454347 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr4:121957805 A>T maps to NM_024574.3 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:121957871 G>A maps to NM_024574.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr4:121958320 G>A maps to NM_024574.3 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr4:121957571 G>A maps to NM_024574.3 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr4:121957424 G>A maps to NM_024574.3 F567F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr4:71200966 A>T maps to NM_033122.3 K71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:87808999 C>T maps to NM_144645.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:184605509 G>A maps to NM_021942.4 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr4:159894424 G>A maps to NM_152543.2 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr4:159590921 T>A did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr4:5966858 G>A maps to ENST00000324058 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr4:5961299 G>A maps to ENST00000324058 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr4:71098716 C>T maps to NM_152997.2 Q22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr4:71099894 C>T maps to NM_152997.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr9:123734243 G>A maps to NM_001735.2 V1348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr19:47823366 C>T maps to ENST00000355085 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr19:47823534 G>A maps to ENST00000355085 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr19:47823942 C>T maps to ENST00000355085 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr19:47823261 C>T maps to ENST00000355085 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr19:47823549 C>T maps to ENST00000355085 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr19:47823684 G>A maps to ENST00000355085 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr5:133295469 C>T maps to NM_020199.2 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr5:134782762 C>T maps to NM_130848.2 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:175772331 G>T maps to ENST00000443967 E835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr5:175722260 C>T maps to ENST00000443967 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr5:36241622 G>T maps to NM_001085411.1 S93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr5:154200896 G>T maps to NM_032385.3 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr5:154199986 A>G maps to NM_032385.3 H297H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:156770214 C>T maps to NM_001001343.3 Q110Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr5:172517871 A>G maps to NM_153607.2 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr5:172535677 C>A maps to NM_153607.2 S425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:37174002 G>A maps to NM_023073.3 L2009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:37179533 C>A maps to NM_023073.3 E1917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr5:37176047 G>A maps to NM_023073.3 Q1981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr5:37173928 G>A maps to NM_023073.3 F2033F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr5:37187900 G>C maps to NM_023073.3 V1285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr5:37186439 T>C maps to NM_023073.3 L1379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr5:64920895 G>C maps to NM_001093755.1 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr5:179274979 G>T maps to NM_016175.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr5:179275017 A>G maps to NM_016175.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr5:147286040 C>G maps to NM_206966.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:125968327 C>T maps to NM_207408.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr5:125967494 C>G maps to NM_207408.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr5:7835578 A>G maps to NM_001089584.1 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr5:159821354 G>A maps to NM_022090.3 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr5:159822088 G>A maps to NM_022090.3 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr5:442598 G>A maps to NM_138464.2 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr5:442649 G>C maps to NM_138464.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr5:169661979 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:169662009 G>A maps to NM_001102609.1 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr5:41203296 C>G maps to NM_001115131.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr5:41159293 C>T maps to NM_001115131.1 K582K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr5:41158835 A>T maps to NM_001115131.1 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr5:41153993 A>G maps to NM_001115131.1 F736F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr6:34214470 G>C maps to NM_178508.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr6:32261222 C>T maps to ENST00000447241 Q409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:34664290 C>T maps to NM_024294.2 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr6:34574586 C>G maps to NM_024294.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:34664338 C>T maps to NM_024294.2 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:43194089 G>A maps to ENST00000509253 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr6:165715279 G>T maps to NM_144980.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr6:37467606 G>A maps to NM_138493.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr6:37451063 C>T maps to NM_138493.2 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr6:30595903 C>G maps to ENST00000376485 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr6:30595654 C>T maps to ENST00000376485 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:30619213 C>T maps to NM_001161376.1 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr6:30618793 C>A maps to NM_001161376.1 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:30620652 A>C maps to NM_001161376.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:47976583 G>A maps to NM_001013732.3 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr6:47846814 G>A maps to NM_001013732.3 R589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:47847058 A>C maps to NM_001013732.3 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr6:47846542 C>T maps to NM_001013732.3 V679V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr6:54025593 C>G maps to ENST00000502396 V832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr6:54095690 C>T maps to ENST00000502396 L966L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr6:53989524 T>C maps to ENST00000502396 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:53989645 C>T maps to ENST00000502396 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr6:53989563 C>T maps to ENST00000502396 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr6:53989533 C>A maps to ENST00000502396 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:4069640 C>T maps to NM_173563.1 W272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:4068965 A>C maps to NM_173563.1 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr6:31079482 C>T maps to NM_014070.2 W218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr6:31079946 G>A maps to NM_014070.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:31080063 G>C maps to NM_014070.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:74150016 C>T maps to NM_138441.2 W343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:74150011 G>T maps to NM_138441.2 S345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr6:43477253 G>C maps to NM_001012974.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr6:88126384 A>C did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:97613183 C>T maps to NM_198468.2 L1053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:97677244 C>A maps to NM_198468.2 E522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr6:97676801 C>T maps to NM_198468.2 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr6:121481249 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr6:121577265 A>G maps to ENST00000275159 Y633Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr6:121577356 G>C maps to ENST00000275159 S603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr6:121562695 G>A maps to ENST00000275159 V720V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:121401952 C>T maps to ENST00000275159 L1287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr6:127796587 G>A maps to NM_001012279.2 D861D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr6:127837621 C>T maps to NM_001012279.2 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr6:109471319 G>C did not map to a codon.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr6:109484116 C>T maps to NM_173830.4 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr6:110567225 G>A maps to NM_001123364.1 Q342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:110620122 A>T did not map to a codon.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr6:133111327 T>C maps to NM_052831.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:133100543 C>G did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr6:133100528 C>A maps to NM_052831.2 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr6:2623699 C>T maps to NM_152554.2 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr6:4087896 C>T maps to NM_001085401.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:107365502 G>A maps to NM_001142470.1 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr6:107365496 C>G maps to NM_001142470.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr6:118790254 G>T maps to NM_001042475.2 S745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr6:118790426 G>A maps to NM_001042475.2 Q688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr6:74073405 G>A maps to NM_001017361.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr6:74072858 C>T maps to NM_001017361.2 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr6:74073363 G>A maps to NM_001017361.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:36291124 G>T maps to NM_001010903.4 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr6:36287384 G>A maps to NM_001010903.4 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:36291964 C>A maps to NM_001010903.4 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr6:36287387 C>G did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:43968405 C>A maps to NM_153246.4 S17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:112420506 C>A maps to NM_001033564.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr6:31692754 C>T maps to NM_138272.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr6:31730896 G>A maps to NM_001039651.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr6:31733740 C>G maps to NM_025258.2 V806V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:31743146 G>A maps to NM_025258.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr6:31627421 T>C maps to NM_021184.3 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr6:31627691 A>C maps to NM_021184.3 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr6:127898408 G>T maps to NM_001010905.1 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:24714635 G>A maps to NM_030939.4 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr6:24716426 T>C maps to NM_030939.4 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr6:170162546 T>C maps to NM_018341.1 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr6:149900972 C>T maps to NM_138785.3 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:149901793 G>T maps to NM_138785.3 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:35706279 C>T maps to NM_145028.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr6:35715174 G>A maps to NM_145028.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:36887409 C>T maps to NM_152734.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:36882093 G>A maps to NM_152734.3 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr6:151857487 G>T maps to ENST00000367290 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr6:151907136 G>A maps to ENST00000367290 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr5:40972586 G>C maps to NM_000587.2 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:40174618 G>C maps to NM_001193311.1 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:40900029 C>T maps to NM_001193311.1 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr7:31735119 C>G maps to NM_006658.4 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr7:42950478 G>A maps to NM_001099858.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr7:6634088 G>A maps to NM_024067.2 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:6629997 C>T maps to NM_024067.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:6639963 C>G maps to NM_024067.2 S362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr7:6630078 G>A maps to NM_024067.2 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr7:6634163 C>T maps to NM_024067.2 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr7:6639679 C>T maps to NM_024067.2 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr7:2586959 G>A maps to NM_152743.3 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr7:2579516 C>G maps to NM_152743.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr7:2578830 C>T maps to NM_152743.3 E584E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr7:6862991 C>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:150028005 G>A maps to NM_138434.2 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:150027531 G>C maps to NM_138434.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr7:148288195 T>A maps to NM_145304.2 L60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:142636690 C>T maps to NM_178829.4 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr7:39612070 G>A maps to NM_020192.3 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr7:30197061 G>A maps to NM_152793.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr7:30185804 G>T maps to NM_152793.2 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:66418352 G>A maps to NM_017994.4 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:66409967 G>A maps to NM_017994.4 W55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr7:99754135 C>T maps to NM_018275.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr7:99753311 C>G maps to NM_018275.3 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr7:43684864 G>A maps to NM_018224.2 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:134853653 C>T maps to NM_024033.2 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:100087044 C>G maps to ENST00000423930 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:100087017 C>G maps to ENST00000423930 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr7:100091378 C>T maps to ENST00000423930 I794I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:100817923 G>A maps to NM_198571.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr7:100816749 C>A maps to NM_198571.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr7:48081093 C>T maps to ENST00000430738 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:48080988 G>A maps to ENST00000430738 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:48081009 C>T maps to ENST00000430738 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr7:120740099 G>T maps to NM_024913.4 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr7:120765939 G>T maps to NM_024913.4 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:120768503 C>T maps to NM_024913.4 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr7:120906784 C>T maps to NM_024913.4 G852G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr7:120935616 C>T maps to NM_024913.4 R998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:112461938 G>A maps to NM_152556.2 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:112462302 G>A maps to NM_152556.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr7:112462116 C>T maps to NM_152556.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:89894676 C>A maps to NM_001039706.2 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:89936244 G>T maps to NM_001039706.2 E766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr7:89939503 G>A maps to NM_001039706.2 V926V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:89887467 G>A maps to NM_001039706.2 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:92158208 C>T maps to NM_032120.2 R28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:92158135 G>A maps to NM_032120.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:57320597 C>T maps to NM_000562.2 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr1:57351742 C>T maps to NM_000562.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr1:57373627 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:57395166 C>T maps to NM_000066.2 K562K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:146279412 C>G maps to ENST00000444534 S200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:69688648 G>T maps to NM_052958.2 G474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr8:69358638 C>G maps to NM_052958.2 S184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr8:69351786 C>T maps to NM_052958.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr8:96281398 C>A maps to NM_177965.3 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr8:40011206 C>T maps to NM_020130.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr8:33369966 G>T maps to NM_001102401.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr8:33367319 G>A maps to NM_001102401.1 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr8:442628 C>A maps to NM_175075.3 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr8:86129719 C>T maps to NM_001099670.1 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr8:86127170 A>C maps to NM_001099670.1 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr8:144654812 C>T maps to NM_001100878.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:10555322 G>A maps to NM_001040032.1 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr8:10555319 C>T maps to NM_001040032.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr8:10555223 C>T maps to NM_001040032.1 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr8:10557758 C>T maps to NM_001040032.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr8:124250181 C>G did not map to a codon.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr8:124253502 G>T maps to NM_032847.1 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr8:124232390 G>A maps to NM_032847.1 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr8:124253562 G>A maps to NM_032847.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr8:124232436 G>C maps to NM_032847.1 S350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr8:12879450 C>T maps to NM_020844.2 C421C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:73993281 C>T maps to NM_153225.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr8:117950662 C>T maps to NM_001025357.2 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:38370102 G>C maps to NM_207412.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr8:38373958 C>T maps to NM_207412.1 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr8:38374030 C>G did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr8:38373934 G>A maps to NM_207412.1 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr5:39306847 T>G maps to NM_001737.3 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr5:39306787 C>T maps to NM_001737.3 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr5:39364494 C>T maps to NM_001737.3 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:98691086 C>G maps to NM_001010895.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr9:98691011 G>A maps to NM_001010895.2 V550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr9:98690413 C>G maps to NM_001010895.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr9:98660208 C>T maps to NM_001010895.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr9:27286301 G>T maps to NM_020641.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr9:130471919 C>A maps to NM_001012502.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr9:131038982 T>C maps to NM_001040011.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:7799695 G>A maps to NM_033428.1 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr9:104239023 G>A maps to NM_032342.1 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr9:35044992 C>G maps to NM_203299.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr9:35045390 C>G maps to NM_203299.2 S922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr9:35043225 C>A maps to NM_203299.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr9:35043078 G>T maps to NM_203299.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr9:139887393 G>C maps to NM_183241.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr9:12775740 C>T maps to NM_203403.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr9:112969748 G>C maps to NM_001012993.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr9:100667173 C>A maps to NM_016481.3 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr9:135447887 C>T maps to NM_207417.1 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr9:135374122 C>G maps to NM_207417.1 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr9:135285702 G>A maps to NM_207417.1 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:135374762 C>T maps to NM_207417.1 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr9:135285813 C>A maps to NM_207417.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr9:139741082 C>T maps to NM_001080482.2 I739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr9:34611038 G>A maps to NM_148179.1 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr9:34402805 C>G did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr9:97844945 G>A maps to NM_001193329.1 K803K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr9:97522289 G>A maps to NM_001193329.1 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr9:97522478 G>C maps to NM_001193329.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr9:77567327 G>T maps to NM_017998.2 S67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:77631214 C>A maps to NM_152420.1 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr9:116187296 A>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:116183391 T>C maps to ENST00000451722 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr9:116176037 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr9:111855809 G>A maps to NM_032012.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr9:111812855 G>C maps to NM_032012.3 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr9:111795590 G>A maps to NM_032012.3 Q864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr9:111853208 C>T maps to NM_032012.3 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr9:86571109 C>A maps to NM_032307.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:86570436 G>A maps to NM_032307.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr9:214919 C>T maps to NM_152569.2 L159L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ZF-A9R7-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:4661988 G>A maps to ENST00000454239 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:71155604 C>T maps to NM_153237.1 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr9:71155529 A>G maps to NM_153237.1 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr9:27566842 C>T maps to NM_018325.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:27561629 G>C maps to NM_018325.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr9:132590499 G>A maps to NM_016520.2 N270N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr9:132597448 C>A maps to NM_016520.2 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr9:90501166 C>T maps to NM_178828.4 Q589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:90497817 C>T maps to NM_178828.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr9:90503511 A>G maps to NM_178828.4 R1370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr9:90497994 C>G maps to NM_178828.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr9:114520465 G>A maps to NM_173521.3 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr9:114454537 G>C maps to NM_173521.3 S1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr9:114454625 G>A maps to NM_173521.3 Q1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr9:74526691 G>A maps to NM_182505.3 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr9:139726190 C>T maps to NM_001173988.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:139726761 G>A maps to NM_001173988.1 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr9:139734252 G>A maps to NM_001173988.1 K623K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr9:135763736 C>T maps to ENST00000372136 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:135763712 C>T maps to ENST00000372136 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:136253247 C>T maps to NM_153710.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr9:136263157 C>T maps to NM_153710.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr9:136256516 G>C maps to NM_153710.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr9:136260779 G>A maps to NM_153710.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr9:135601227 G>C maps to NM_152572.2 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr9:135702365 G>C maps to NM_152572.2 S211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:135703439 G>A maps to NM_152572.2 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr8:86245786 A>T maps to NM_001738.3 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:49713290 C>T maps to NM_001082534.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr19:49143533 G>T maps to NM_001217.3 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr19:49148880 A>C maps to NM_001217.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:49143471 G>A maps to NM_001217.3 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:150235592 G>T maps to NM_012113.1 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:58236631 G>A maps to NM_000717.3 Q262Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr17:58227416 C>T maps to NM_000717.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr17:58227430 G>A maps to NM_000717.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr16:87969913 C>T did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr16:87921737 G>A maps to NM_001739.1 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr23:15790686 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr23:15800716 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:15768237 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr1:9018967 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr16:66881068 C>T maps to NM_005182.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr16:66881027 C>T maps to NM_005182.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr8:61192271 G>A maps to NM_004056.4 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:231683404 C>T maps to NM_001130850.1 Q338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr13:49933857 G>A maps to NM_001079670.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:227171507 C>T maps to NM_020247.4 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr1:227173037 C>G maps to NM_020247.4 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:227152912 C>T maps to NM_020247.4 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:227149127 C>T maps to NM_020247.4 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:227170377 G>C did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr22:24562742 C>G maps to NM_012295.3 S1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr22:24468353 C>T maps to NM_012295.3 V842V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr22:24472151 C>A maps to NM_012295.3 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr22:24456600 C>A maps to NM_012295.3 I538I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr18:20833800 C>G maps to NM_001100619.2 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr18:20837243 C>T maps to NM_001100619.2 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr20:60967522 G>C maps to NM_031215.2 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:121098023 C>T maps to NM_001033677.1 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:67223205 G>T maps to NM_145200.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:67223785 C>T maps to NM_145200.3 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr11:67223675 C>T maps to NM_145200.3 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr19:48537490 G>A maps to NM_019855.3 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr19:48537544 C>T maps to NM_019855.3 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr22:30125135 C>T maps to NM_182527.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr18:21723369 G>A maps to NM_138644.1 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:65145287 G>A maps to ENST00000371073 V1085V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr1:65120375 C>T maps to ENST00000371073 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:65131826 C>T maps to ENST00000371073 I788I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:65098404 C>T maps to ENST00000371073 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:65129432 C>G maps to ENST00000371073 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:13616822 G>C maps to NM_023035.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr19:13409699 C>T maps to NM_023035.2 W920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:13470506 C>T maps to NM_023035.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:13411422 C>T maps to NM_023035.2 Q744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr19:13476200 A>G maps to NM_023035.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr19:13419049 G>C maps to NM_023035.2 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr19:13616858 T>C maps to NM_023035.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:13325351 G>T maps to NM_023035.2 S1938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr19:13563772 G>A maps to NM_023035.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr9:140991036 C>G maps to ENST00000277549 V1733V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr9:140811876 C>G maps to ENST00000277549 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr9:140777293 G>C maps to ENST00000277549 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr9:140938262 G>A maps to ENST00000277549 K1109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr9:140917591 C>T maps to ENST00000277549 F800F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr9:140865957 G>A maps to ENST00000277549 W487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr9:141016297 C>A maps to ENST00000277549 G2290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr9:140870461 C>T maps to ENST00000277549 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr9:140948326 G>A maps to ENST00000277549 L1280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr9:140907666 C>T maps to ENST00000277549 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr12:2595324 C>A maps to NM_199460.2 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:2795356 A>G maps to NM_199460.2 E1985E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:2224702 C>G maps to NM_199460.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:2775902 G>A maps to NM_199460.2 P1574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:2742832 C>T maps to NM_199460.2 L1309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr12:2614032 G>A maps to NM_199460.2 W380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:2690860 C>A maps to NM_199460.2 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr12:2788755 G>A maps to NM_199460.2 E1794E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr12:2760831 C>T maps to NM_199460.2 S1372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr12:2566822 G>A maps to NM_199460.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr12:2595328 C>T maps to NM_199460.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr12:2742832 C>T maps to NM_199460.2 L1309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:2706607 A>C maps to NM_199460.2 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:53844149 C>G maps to NM_001128840.1 S2006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr3:53796062 C>T maps to NM_001128840.1 L1275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr3:53809939 G>A maps to NM_001128840.1 E1410E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:53783405 C>T maps to NM_001128840.1 F1142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr3:53820933 A>T maps to NM_001128840.1 G1626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr3:53835317 C>G maps to NM_001128840.1 L1758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr3:53769490 C>T maps to NM_001128840.1 A904A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:53837569 C>T maps to NM_001128840.1 Y1852Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr3:53815626 T>C maps to NM_001128840.1 A1575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:53839033 A>G maps to NM_001128840.1 R1870R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr1:181548262 T>A maps to ENST00000357570 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:181702025 C>A maps to ENST00000357570 S935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr1:181689975 C>T maps to ENST00000357570 I647I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:181767564 G>A maps to ENST00000357570 A2179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr1:181705555 C>T maps to ENST00000357570 F1136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr1:181479642 C>T maps to ENST00000357570 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr1:181754943 C>T maps to ENST00000357570 P1925P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr1:181707500 A>G did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:181745298 C>T maps to ENST00000357570 S1734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr1:181732600 C>T maps to ENST00000357570 L1583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMJ-01A-11D-A42E-08 chr1:181726214 G>T maps to ENST00000357570 E1428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:181741345 C>T maps to ENST00000357570 F1706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:181767825 C>T maps to ENST00000357570 I2266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr23:49071898 G>A did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr23:49079026 C>T did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr23:49070627 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:49079297 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr23:49062080 C>T did not map to a codon.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr23:49068424 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr23:49071569 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr23:49065841 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:49066424 C>G did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:49074241 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:49070722 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr17:48681581 C>A maps to NM_018896.3 I1412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr17:48681611 C>T maps to NM_018896.3 F1422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr17:48676976 G>A maps to NM_018896.3 E1149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr17:48695428 C>T maps to NM_018896.3 L1749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr17:48669429 C>T maps to NM_018896.3 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:48696035 C>T maps to NM_018896.3 D1816D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:48669296 G>T did not map to a codon.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr17:48703808 C>T maps to NM_018896.3 S2277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr17:48696224 C>T maps to NM_018896.3 S1879S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:1267917 G>A did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr16:1254340 C>T maps to NM_021098.2 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr16:1261805 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr16:1270948 C>G maps to NM_021098.2 P2339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:1260647 G>A maps to NM_021098.2 V1345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr22:40066080 C>T maps to NM_021096.3 F1411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:40058010 C>T maps to NM_021096.3 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr22:40059830 C>T maps to NM_021096.3 I1194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr22:40059827 G>A maps to NM_021096.3 Q1193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr22:40059827 G>A maps to NM_021096.3 Q1193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr22:39966822 C>T maps to NM_021096.3 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr22:39996538 C>T maps to NM_021096.3 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr1:201016692 G>T maps to NM_000069.2 T1501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:201060840 G>C maps to NM_000069.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:201030502 G>A maps to NM_000069.2 I1049I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:201056979 G>A maps to NM_000069.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:201030511 G>A maps to NM_000069.2 I1046I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:201035413 C>T maps to NM_000069.2 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:201027538 G>A maps to NM_000069.2 I1202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr1:201038635 C>T maps to NM_000069.2 A818A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr1:201054594 G>A maps to NM_000069.2 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:201052308 G>A maps to NM_000069.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:201061109 C>T maps to NM_000069.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr1:201079381 G>A maps to NM_000069.2 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr1:201046203 G>A maps to NM_000069.2 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr1:201035007 G>A maps to NM_000069.2 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr1:201029818 G>A maps to NM_000069.2 L1127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr7:81598263 C>T maps to NM_000722.2 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr7:81593585 A>C maps to NM_000722.2 Y888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr7:81635095 C>A maps to NM_000722.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:50471823 C>A maps to ENST00000435965 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr3:50421756 C>T maps to ENST00000435965 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:50402599 C>T maps to ENST00000435965 Q1045Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr3:54871247 G>A maps to NM_018398.2 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr3:54925414 C>T maps to NM_018398.2 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr3:54604056 C>T maps to NM_018398.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:2017149 G>A maps to NM_172364.4 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr12:2017163 C>A maps to NM_172364.4 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:37347814 G>C maps to NM_000723.3 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr17:37343122 G>A maps to NM_000723.3 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:37340338 G>C maps to NM_000723.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr17:37343110 G>A maps to NM_000723.3 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:49219013 G>A maps to NM_000725.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr12:49220792 G>T maps to NM_000725.2 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr2:152737379 G>A maps to NM_000726.3 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr2:152739811 G>A maps to NM_000726.3 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:65052308 C>T maps to NM_000727.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:36960928 C>T maps to NM_006078.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr22:36960871 C>T maps to NM_006078.3 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr22:36960928 C>G maps to NM_006078.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr22:36962430 G>A maps to NM_006078.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr16:24372923 C>T maps to NM_006539.3 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr16:24268125 C>T maps to NM_006539.3 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr16:24373075 C>G maps to NM_006539.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr16:24372973 C>T maps to NM_006539.3 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:65026585 C>A maps to NM_014405.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr17:64961104 C>T maps to NM_014405.3 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:64961104 C>T maps to NM_014405.3 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr17:64961110 C>T maps to NM_014405.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:64880759 C>T maps to NM_014404.1 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:64876672 G>C did not map to a codon.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr19:54515343 C>T maps to NM_145814.1 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr19:54444721 A>G did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr19:54418652 C>T maps to NM_031896.4 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr19:54483175 C>G maps to NM_031895.5 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr19:54483148 C>T maps to NM_031895.5 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr2:27465811 C>T maps to NM_004341.3 R2151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr2:27449409 G>C maps to NM_004341.3 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr2:27454928 G>T maps to NM_004341.3 E828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:27447626 G>A maps to NM_004341.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr2:27462281 G>A maps to NM_004341.3 V1779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr2:27447626 G>T maps to NM_004341.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:27456907 T>G maps to NM_004341.3 G1144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:27464070 C>T maps to NM_004341.3 S1928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr3:86028350 C>T maps to NM_153184.3 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr3:86010774 G>A maps to NM_153184.3 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr3:86115926 C>T maps to NM_153184.3 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:159169586 C>T maps to NM_021189.3 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr1:159166752 C>T maps to NM_021189.3 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:159161792 G>A maps to NM_021189.3 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:159161861 G>A maps to NM_021189.3 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:159166684 C>T maps to NM_021189.3 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:159166680 C>G maps to NM_021189.3 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:159162422 C>T maps to NM_021189.3 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr19:44129329 G>A maps to NM_145296.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr19:44131814 G>C maps to NM_145296.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr3:62631491 G>A maps to ENST00000383709 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr3:62484935 T>C maps to ENST00000383709 V869V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr3:62860632 G>A maps to ENST00000383709 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr3:62477078 C>T maps to ENST00000383709 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:62739199 C>T maps to ENST00000383709 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr3:62467438 A>T maps to ENST00000383709 T1044T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr3:62464048 G>A maps to ENST00000383709 D1072D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr3:62860617 G>A maps to ENST00000383709 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr3:62636737 C>T maps to ENST00000383709 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr7:122261660 C>T maps to NM_001167940.1 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:122526106 G>A maps to NM_001167940.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr7:122111490 G>A maps to NM_001167940.1 V708V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr7:121960344 C>T maps to NM_001167940.1 L1259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr6:7373862 G>A maps to NM_001170692.1 Q397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr8:91072499 A>G maps to NM_004929.2 N229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr8:91094303 G>A maps to NM_004929.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr16:71417913 C>G maps to NM_001740.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr16:71411634 C>T maps to NM_001740.4 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr11:14989312 C>T maps to NM_001033953.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:54115351 C>T maps to NM_020898.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:46933491 C>T maps to ENST00000448105 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr17:46919185 A>G maps to ENST00000448105 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr7:93055751 C>T maps to NM_001164737.1 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr7:93108737 G>T maps to NM_001164737.1 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr7:93055889 G>A maps to NM_001164737.1 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:188211113 G>A maps to NM_005795.4 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr2:188243734 C>T maps to NM_005795.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr7:134620516 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr7:134618713 C>A maps to NM_033138.3 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr7:134645281 A>C did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr7:134617873 G>A maps to NM_033138.3 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr10:105215486 G>A maps to NM_001001412.3 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr10:105218184 G>A maps to NM_001001412.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr10:105215036 G>C maps to NM_001001412.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:105207265 G>C maps to NM_015916.4 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr10:105207265 G>C maps to NM_015916.4 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr10:5567431 C>T maps to NM_005185.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr10:5541088 G>T maps to NM_017422.4 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr7:71252774 C>G maps to NM_031468.3 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr7:71571256 A>G maps to NM_031468.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr7:71252774 C>G maps to NM_031468.3 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:13054367 C>T maps to NM_004343.3 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:13050909 C>T maps to NM_004343.3 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr19:13051184 G>A maps to NM_004343.3 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:13050906 C>T maps to NM_004343.3 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr19:16594791 C>T maps to NM_145046.3 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:16601208 C>T maps to NM_145046.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr19:16601208 C>T maps to NM_145046.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr19:16606663 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:9803375 G>A maps to NM_003656.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr3:9801411 C>T maps to NM_003656.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr3:9803354 G>T maps to NM_003656.3 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr3:9802406 G>C maps to NM_003656.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:12856253 C>G maps to NM_153498.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr1:209783232 G>C maps to NM_020439.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:149669140 G>A maps to NM_015981.3 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr5:149607849 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr5:149618311 C>A did not map to a codon.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr5:149602568 C>T maps to NM_015981.3 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr7:44259780 G>A maps to NM_001220.4 D627D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr7:44281933 C>A maps to NM_001220.4 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:44364972 G>C maps to NM_001220.4 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr7:44286781 G>A maps to NM_001220.4 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr7:44266118 G>A maps to NM_001220.4 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr7:44266211 C>T maps to NM_001220.4 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr7:44302619 C>T maps to NM_001220.4 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:75574820 G>C maps to ENST00000423381 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:75609036 G>A maps to ENST00000423381 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr10:75576811 C>G maps to ENST00000423381 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr10:75577298 C>T maps to ENST00000423381 E459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr10:75609036 G>A maps to ENST00000423381 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:75609036 G>A maps to ENST00000423381 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr10:75609036 G>A maps to ENST00000423381 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:110818484 C>T maps to NM_001744.4 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr5:110784839 C>G maps to NM_001744.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr5:110560255 C>G maps to NM_001744.4 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr5:110712637 T>C maps to NM_001744.4 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr5:110782427 G>A maps to NM_001744.4 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:3779564 G>A maps to ENST00000381771 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr12:121693607 C>T did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr12:121706439 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr12:121678659 G>A maps to NM_006549.3 R537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr5:134074396 G>A maps to NM_001745.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:134074447 G>A maps to NM_001745.2 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr5:134086447 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:138713632 G>A maps to ENST00000409386 L969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr9:138703238 G>A maps to ENST00000409386 V1586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr9:138706963 G>C maps to ENST00000409386 P1506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr1:200818422 G>A maps to ENST00000236925 E853E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr1:200729986 C>T maps to ENST00000236925 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:200818297 C>T maps to ENST00000236925 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:200801404 G>C maps to ENST00000236925 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:200817711 T>C maps to ENST00000236925 N616N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:7724194 A>T maps to NM_015215.2 K530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:7723701 G>A maps to NM_015215.2 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FH-01A-11D-A38G-08 chr1:7811339 C>T maps to NM_015215.2 Q1591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr1:7309564 C>A maps to NM_015215.2 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr1:7724544 G>A maps to NM_015215.2 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr1:7798175 C>T maps to NM_015215.2 I1272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr1:7796515 C>G maps to NM_015215.2 S1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr1:7798259 C>G maps to NM_015215.2 L1300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr1:7725069 C>T maps to NM_015215.2 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:7792598 G>C maps to NM_015215.2 A1002A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr17:4884615 C>A maps to NM_015099.3 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:4889553 G>A maps to NM_001171168.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr17:4876990 C>T maps to NM_015099.3 W697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr17:4881808 G>A maps to NM_015099.3 C585C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr12:67703714 G>A maps to NM_018448.3 L1020L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr12:67703817 G>T maps to NM_018448.3 E1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:67700276 A>C maps to NM_018448.3 A943A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr12:67663511 G>C maps to NM_018448.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMJ-01A-11D-A42E-08 chr12:67700354 G>A maps to NM_018448.3 R969R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr3:12861666 G>A maps to NM_001162499.1 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr3:12861591 A>G maps to NM_001162499.1 P984P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:12845085 C>A maps to NM_001162499.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr3:12869075 C>T maps to NM_001162499.1 D1116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr17:76993383 G>A maps to NM_138793.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr5:179143167 C>T maps to ENST00000415618 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr5:179135269 C>G maps to ENST00000415618 S147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr5:179151699 C>T maps to ENST00000415618 Q556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr5:179143172 C>G maps to ENST00000415618 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:40529929 C>G maps to NM_001105530.1 S109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr6:17539633 T>C maps to NM_006366.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr6:17507398 G>A did not map to a codon.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr6:17507500 G>A maps to NM_006366.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr6:17514184 A>C maps to NM_006366.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr6:17541216 C>G maps to NM_006366.2 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:85622016 C>T maps to NM_001747.2 *349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:85625865 C>A maps to NM_001747.2 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr2:85622042 G>A maps to NM_001747.2 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr2:85626396 G>C maps to NM_001747.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:64972253 C>G maps to NM_005186.3 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr11:64950984 C>G maps to NM_005186.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:64950978 C>T maps to NM_005186.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr11:64978303 C>T maps to NM_005186.3 D693D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr11:64950402 C>A maps to NM_005186.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr11:64978729 G>T did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:64977855 G>A maps to NM_005186.3 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr11:64954753 G>C maps to NM_005186.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr11:64977816 C>A maps to NM_005186.3 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr11:64956165 G>T maps to NM_005186.3 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr11:64950957 C>G maps to NM_005186.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr2:241531490 G>A maps to NM_023083.3 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:44140777 C>T maps to NM_007058.3 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr19:39226177 G>T maps to NM_144691.3 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr19:39225498 G>C maps to NM_144691.3 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:30976030 G>A maps to ENST00000295055 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr2:30957381 G>A maps to ENST00000295055 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:30954217 C>A maps to ENST00000295055 E659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr2:30965215 G>A maps to ENST00000295055 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:223959544 C>T maps to NM_001748.4 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr15:42691774 C>T maps to NM_000070.2 Q427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr15:42703969 G>C maps to NM_000070.2 *822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr15:42702645 C>A maps to NM_000070.2 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr11:76804825 G>A maps to ENST00000360841 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr11:76796097 G>T did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:76825377 G>C maps to ENST00000360841 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr11:76823765 C>G maps to ENST00000360841 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr11:76823777 C>T maps to ENST00000360841 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr11:76830152 G>T maps to ENST00000360841 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr11:76795979 G>A maps to ENST00000360841 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:110491100 T>G did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:110490613 G>A did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:110491216 T>C did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr23:110489910 T>C did not map to a codon.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr23:110494220 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr3:15265035 G>A maps to NM_014296.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr3:15283749 T>G maps to NM_014296.2 V618V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr3:15262299 G>A maps to NM_014296.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr3:15258961 C>A maps to NM_014296.2 S81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr1:230903407 C>T maps to NM_006615.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:230903448 C>T maps to NM_006615.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr16:55601051 G>A maps to NM_032330.1 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr11:34097865 T>C maps to NM_005898.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr11:34107637 C>T maps to NM_005898.4 Q332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr11:34097785 C>T maps to NM_005898.4 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr12:30863383 G>A maps to NM_001002259.1 Q946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:30881857 C>T maps to NM_001002259.1 Q502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr12:30906678 G>A maps to NM_001002259.1 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:30872127 G>T maps to NM_001002259.1 S727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:30879019 C>A maps to NM_001002259.1 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr19:5915331 G>A maps to ENST00000394521 *323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr19:5915248 C>T maps to ENST00000394521 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:75676042 G>A maps to NM_032606.3 Q553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr12:18891513 C>A maps to NM_033328.2 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr1:19670913 T>C maps to ENST00000375145 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:19683146 T>G maps to ENST00000375145 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr22:37915012 C>T maps to NM_014550.3 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:37902201 G>C maps to NM_014550.3 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr22:37904563 C>T maps to NM_014550.3 E345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr22:37915039 G>T maps to NM_014550.3 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr7:2953088 C>A maps to NM_032415.4 E951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr7:2978459 C>T maps to NM_032415.4 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:2979559 G>A maps to NM_032415.4 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr7:2984028 C>T maps to NM_032415.4 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:2957019 C>G did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:2978459 C>T maps to NM_032415.4 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr7:2956959 G>C maps to NM_032415.4 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr7:2953005 G>A maps to NM_032415.4 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr7:2976843 G>A maps to NM_032415.4 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr17:78162252 G>A maps to NM_024110.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr17:78162186 G>C maps to NM_024110.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr17:78166303 C>G maps to NM_024110.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr17:78179328 G>C did not map to a codon.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr17:78180860 C>T maps to NM_024110.2 N928N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr11:104912207 G>A maps to NM_001017534.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr11:105009558 G>C maps to NM_021571.3 S85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr11:105009568 G>A maps to NM_021571.3 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr5:40843578 A>G maps to NM_032587.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr5:40852631 C>T maps to NM_032587.3 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr5:40843461 G>A maps to NM_032587.3 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr9:139265141 G>C maps to NM_052813.4 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr9:139264234 C>T maps to NM_052813.4 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr9:139262241 G>A maps to NM_052813.4 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr13:111287894 C>A maps to NM_018210.2 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr19:11018763 G>T maps to NM_199141.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr19:11018764 G>T maps to NM_199141.1 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr19:11031349 C>T maps to NM_199141.1 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr19:11032084 G>A maps to NM_199141.1 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr11:67191687 T>C maps to NM_001166222.1 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr11:3026646 C>T maps to NM_001014437.2 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr11:3069172 C>T maps to NM_001014437.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:3026646 C>T maps to NM_001014437.2 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr11:3022396 C>A maps to NM_001014437.2 E815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr13:111319755 C>A maps to NM_024537.2 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr13:111296829 C>A maps to NM_024537.2 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr5:71015206 G>A maps to NM_004291.3 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr12:25261642 C>A maps to NM_018272.3 E670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr12:25311495 C>T maps to NM_018272.3 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr17:38318274 G>A maps to NM_007359.4 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:38297459 G>T maps to NM_007359.4 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr17:38323833 C>T maps to NM_007359.4 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr15:44630078 C>G maps to NM_138423.3 S232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr15:40916775 T>C maps to NM_170589.3 Y1464Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:40917630 C>T maps to NM_170589.3 I1749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:40913170 G>T maps to NM_170589.3 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr15:40915697 C>G maps to NM_170589.3 S1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr15:40914271 C>T maps to NM_170589.3 Q630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr15:40912935 T>C maps to NM_170589.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:94175011 C>T maps to NM_022900.4 N544N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr7:94163032 C>T maps to NM_022900.4 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr7:94174870 C>T maps to NM_022900.4 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr7:94166998 G>A maps to NM_022900.4 K353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr7:94173796 A>G maps to NM_022900.4 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:41782185 C>T did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:41414877 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:41437655 C>A did not map to a codon.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr23:41414859 C>T did not map to a codon.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr23:41448779 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr23:41437602 T>C did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:41379734 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr23:41413128 C>T did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:41416282 A>G did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:41524685 A>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:2237187 C>A maps to NM_020764.3 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr16:2239140 G>C maps to NM_020764.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:2237254 C>A maps to NM_020764.3 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:2239140 G>T maps to NM_020764.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr17:73498742 A>T maps to NM_020753.3 P804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr17:73500694 G>C maps to NM_020753.3 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:104899925 C>A maps to NM_033292.2 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr11:104897664 C>T maps to NM_033292.2 W340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:104900515 C>T maps to NM_033292.2 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:202073796 C>T maps to NM_032977.3 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr2:202070672 C>T maps to NM_032977.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:15164701 G>T maps to NM_012114.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr7:142989484 G>A maps to NM_032982.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr7:142985598 G>T maps to NM_032982.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr7:143000970 G>A maps to NM_032982.2 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr4:185550476 C>T maps to NM_032991.2 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr4:185550578 G>T maps to NM_032991.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:104821780 G>A maps to NM_001225.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:104877903 C>T maps to NM_001136112.1 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr10:115480793 G>A maps to NM_033338.4 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:202149750 C>T maps to NM_001080125.1 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr2:202149665 C>T maps to NM_001080125.1 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr2:202150029 C>T maps to NM_001080125.1 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr2:202151180 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:202150038 C>T maps to NM_001080125.1 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr6:90574019 G>A maps to NM_012115.3 V864V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr6:90573428 T>A maps to NM_012115.3 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:15821947 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMW-01A-11D-A42E-08 chr1:15844668 T>C maps to NM_001229.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:160165314 C>T maps to NM_001231.4 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:160167376 G>T maps to NM_001231.4 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:116245547 G>A maps to NM_001232.3 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:121994735 G>C maps to NM_001178065.1 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr20:55027047 C>G maps to NM_020356.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:55033554 C>T maps to NM_020356.3 Q705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr20:55012584 C>T maps to NM_020356.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr20:55026996 C>G maps to NM_020356.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr5:96082068 A>G maps to ENST00000508830 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:10720281 G>A maps to NM_001079843.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr1:10713995 C>T maps to NM_001079843.1 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr1:10715783 G>A maps to NM_001079843.1 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:10715771 G>A maps to NM_001079843.1 D533D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:10725290 G>A maps to NM_001079843.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:10699976 G>A maps to NM_001079843.1 F1434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr1:10699862 C>T maps to NM_001079843.1 T1472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr11:65784632 G>A maps to NM_053054.3 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr11:65786338 C>T maps to NM_053054.3 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:65787671 C>T did not map to a codon.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr15:43939558 C>T maps to NM_172095.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr15:43932620 C>T maps to NM_172095.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr15:43931839 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:134332198 C>T maps to NM_178019.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr5:134331985 C>T maps to NM_178019.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr5:134331967 G>A maps to NM_178019.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr5:134346109 G>A maps to NM_178019.2 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:26517171 C>G maps to NM_198137.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr14:92088186 C>T maps to NM_024764.2 K675K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr19:38860867 C>T maps to NM_021185.4 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:38860797 G>A did not map to a codon.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr19:38853418 G>T maps to NM_021185.4 E808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr7:116166724 C>G maps to NM_001753.4 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:8787525 C>T maps to NM_001234.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr3:8787492 C>G maps to NM_001234.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr10:74128015 G>T maps to NM_006077.3 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr10:74234917 C>T maps to NM_006077.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr20:32217652 G>A maps to NM_005093.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr20:32207402 A>G maps to NM_005093.3 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr20:32232408 C>G maps to NM_005093.3 S591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr20:32212723 C>T maps to NM_005093.3 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr20:32211018 C>G maps to NM_005093.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr16:88952448 G>A maps to NM_005187.5 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr16:88958894 T>G did not map to a codon.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr11:119170368 C>T maps to NM_005188.2 Q867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:119170253 G>A maps to NM_005188.2 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr11:119149278 C>T maps to NM_005188.2 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr11:119142468 C>T maps to NM_005188.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:105438983 G>A maps to NM_170662.3 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:105459360 C>G maps to NM_170662.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:105421028 G>C maps to NM_170662.3 S623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:45285643 C>G maps to NM_012116.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr19:45296768 G>A maps to NM_012116.3 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:45287646 G>A maps to NM_012116.3 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr7:107399523 G>A maps to NM_024814.2 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr7:107399328 G>A maps to NM_024814.2 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr16:49313317 G>C maps to NM_004352.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr18:70205476 C>T maps to NM_182511.3 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr20:54579152 G>A maps to NM_080617.4 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47S-01A-11D-A23U-08 chr21:37445141 G>T maps to NM_001757.2 G266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr21:37445053 G>A maps to NM_001757.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr4:169927998 G>A maps to NM_032783.4 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr4:169931102 G>A maps to NM_032783.4 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr21:44479364 C>T maps to ENST00000398168 K398K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr9:70871868 G>T maps to NM_201453.2 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:77758612 G>A maps to NM_005189.2 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr17:77758354 T>G maps to NM_005189.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr17:77758198 G>A maps to NM_005189.2 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:77808876 C>A maps to NM_003655.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:77808681 G>C maps to NM_003655.2 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr17:77811652 C>A maps to NM_003655.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr17:77808234 G>A maps to NM_003655.2 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr17:77808540 G>A maps to NM_003655.2 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr17:77808593 C>A maps to NM_003655.2 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:54651350 C>T maps to NM_012117.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr22:39263131 C>T maps to NM_014292.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMJ-01A-11D-A42E-08 chr22:39262384 C>A maps to NM_014292.3 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr22:39534664 C>T maps to NM_175709.3 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:77768459 G>A maps to NM_020649.2 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr22:39064088 G>A maps to NM_015373.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:14040948 G>C maps to NM_017721.4 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:14028881 G>A did not map to a codon.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr19:14040215 C>G maps to NM_017721.4 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr19:14040912 G>A maps to NM_017721.4 R911R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:52820519 G>A maps to NM_032449.2 F783F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr4:15516472 C>T maps to NM_001080522.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr4:15569098 C>T maps to NM_001080522.2 L1094L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr4:15542458 G>A did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr10:97775977 C>T maps to NM_001159747.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:97791680 T>C maps to NM_001159747.1 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr10:70516174 C>T maps to NM_018237.2 R591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr10:70549494 G>A maps to NM_018237.2 L1072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr18:57363927 C>A maps to NM_133459.3 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:66564536 G>T maps to NM_024781.2 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr18:66513651 G>A maps to NM_024781.2 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr18:66721301 G>A maps to NM_024781.2 Q490Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:42979947 G>A maps to NM_213607.1 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr17:42979926 G>A maps to NM_213607.1 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:15121756 G>A maps to NM_173482.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr2:219896380 C>T did not map to a codon.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr2:219884301 C>T maps to NM_194302.2 L1133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr2:219888838 G>A maps to NM_194302.2 P831P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr2:219894289 G>T maps to NM_194302.2 C495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr2:219892614 G>A maps to NM_194302.2 V656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr2:219886643 T>C maps to NM_194302.2 E996E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr2:219875691 T>G maps to NM_194302.2 S1328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:74619016 C>G maps to NM_138357.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:47769275 C>A maps to NM_145020.3 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr18:47777949 C>G maps to NM_145020.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr18:47765069 G>A maps to NM_145020.3 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:186379493 G>A maps to NM_152775.3 Y749Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr4:186392203 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr4:186380147 T>C maps to NM_152775.3 Q531Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr4:186379656 G>C maps to NM_152775.3 S695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr4:185599490 C>G maps to NM_152683.2 S317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr16:58296314 C>T maps to NM_014157.3 H218H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr16:58287957 G>C maps to NM_014157.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:48801463 G>T maps to NM_144577.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:48800463 C>G maps to NM_144577.3 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr19:48807270 G>A maps to NM_144577.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:48807270 G>A maps to NM_144577.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:131098586 A>C maps to NM_032357.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr22:21988322 A>T maps to NM_152612.2 K29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr22:21988429 G>A maps to NM_152612.2 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr22:29177152 G>T maps to NM_173510.2 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr22:29176963 G>T maps to NM_173510.2 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr23:48921476 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr23:48925162 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr23:48922602 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr23:48925324 G>C did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr23:48925200 C>T did not map to a codon.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr2:27850501 C>T maps to ENST00000435516 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:27850057 C>T maps to ENST00000435516 K367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:27850300 C>T maps to ENST00000435516 Q286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr19:33444637 G>A maps to NM_032816.3 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr19:33439189 G>A maps to NM_032816.3 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr19:33392308 C>T maps to NM_032816.3 Q525Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr19:33439222 G>A maps to NM_032816.3 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr5:68588042 C>T maps to NM_176816.3 W357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr5:68603837 G>A maps to NM_176816.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr5:68602651 T>C maps to NM_176816.3 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr7:31683122 C>T maps to NM_194300.2 S713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr7:31682388 C>T maps to NM_194300.2 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:31682706 G>T maps to NM_194300.2 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr7:31611745 C>T maps to NM_194300.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr7:31683173 C>T maps to NM_194300.2 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr7:31692217 T>C maps to NM_194300.2 T970T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr7:31682891 A>T maps to NM_194300.2 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr7:31682826 G>T maps to NM_194300.2 E615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:42777312 C>T maps to NM_144719.3 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr3:42777324 C>T maps to NM_144719.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr19:13873231 G>A maps to NM_030818.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:13870052 C>T maps to NM_030818.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:92935286 G>T maps to NM_017667.2 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr22:42209813 C>T maps to NM_024821.2 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr22:42209301 C>T maps to NM_024821.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr16:57761218 G>A maps to NM_032269.5 E698E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr16:57736039 G>T maps to NM_032269.5 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:57732920 C>T maps to NM_032269.5 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:128452892 G>A maps to NM_022742.3 L891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr7:128446740 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr7:128452802 G>A maps to NM_022742.3 Q861Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr7:128455856 G>T maps to NM_022742.3 E1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr2:109455739 C>T maps to NM_144978.1 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:109455756 G>A maps to NM_144978.1 Q441Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr2:109492687 G>A maps to NM_144978.1 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:123634089 G>A maps to NM_022757.4 Q759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr3:123649971 C>T maps to NM_022757.4 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr2:223168710 G>A maps to NM_153038.1 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:179733998 C>A maps to NM_173648.3 E747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr2:179730589 C>T maps to NM_173648.3 E876E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:74708005 G>A maps to ENST00000393965 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:74701741 G>A maps to ENST00000393965 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr17:16593761 G>A maps to NM_014695.1 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:16638077 G>A maps to NM_014695.1 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr17:16667285 G>T maps to NM_014695.1 E1299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:16667297 G>T maps to NM_014695.1 E1303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr17:18498090 G>A did not map to a codon.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr17:20799063 C>T maps to NM_001004306.1 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr7:76908130 G>A maps to NM_020879.2 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr10:106209908 C>G maps to NM_001008723.1 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr10:106139899 G>A maps to NM_001008723.1 Q429Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:106209890 G>A maps to NM_001008723.1 E813E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr10:106139803 C>T maps to NM_001008723.1 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:159035485 A>G maps to NM_138803.3 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr4:24839879 C>T maps to NM_001130726.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:24836594 C>G maps to NM_001130726.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:11533472 G>A maps to NM_145045.4 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr19:11534674 T>C maps to NM_145045.4 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr19:11537745 G>A maps to NM_145045.4 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:119061143 G>C maps to NM_001145018.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr11:119061131 C>G maps to NM_001145018.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:49897811 C>T maps to NM_144688.4 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:49901325 G>C maps to NM_144688.4 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr22:30772532 C>T maps to NM_001017437.2 C686C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr22:30772605 G>T maps to NM_001017437.2 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr4:77290739 C>A maps to NM_001042784.1 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr4:77252543 C>T maps to NM_001042784.1 S961S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr4:77253644 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr4:77305782 C>T maps to NM_001042784.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr4:77288668 C>T maps to NM_001042784.1 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:77303763 G>A maps to NM_001042784.1 Q305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr4:77292580 G>A maps to NM_001042784.1 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr4:77292651 G>C maps to NM_001042784.1 S356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr4:77292662 G>A maps to NM_001042784.1 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr4:77305449 C>A maps to NM_001042784.1 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr4:77288710 G>A maps to NM_001042784.1 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr4:77288731 G>A maps to NM_001042784.1 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr1:93680429 G>A maps to NM_206886.2 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:93649604 C>T maps to NM_206886.2 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:93646362 C>T maps to NM_206886.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:93677789 A>G maps to NM_206886.2 E607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:93646272 C>T maps to NM_206886.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:159858267 G>A maps to NM_012337.2 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr1:159842876 G>A maps to NM_012337.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:159842831 C>G maps to NM_012337.2 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr1:26584702 C>G maps to NM_022778.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:26595967 G>A maps to NM_022778.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:26584194 G>A maps to NM_022778.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:26584195 A>T maps to NM_022778.2 K338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:49106024 A>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr1:43273168 G>T maps to NM_199342.3 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:44461718 C>T maps to NM_152499.1 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr1:44457957 C>T maps to NM_152499.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr1:3672129 C>T maps to NM_152492.2 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr1:3669320 C>G maps to NM_152492.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr1:3677873 G>A maps to NM_152492.2 Q247Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr1:3677906 C>G maps to NM_152492.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:3673381 C>T maps to NM_152492.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:3673348 G>A maps to NM_152492.2 K202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr6:139101060 G>A maps to NM_015439.2 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:139094927 G>A maps to NM_015439.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr6:139097340 C>A maps to NM_015439.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr6:139094891 C>G maps to NM_015439.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:32669914 G>T maps to ENST00000421922 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr10:13040394 C>A maps to NM_031455.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr1:43102992 A>T maps to NM_001080850.2 K528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr1:43004856 C>G maps to NM_001080850.2 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr1:43032077 C>T maps to NM_001080850.2 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr3:49249248 C>T maps to NM_178173.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr3:49249259 C>A maps to NM_178173.3 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr3:49274118 G>A maps to NM_178173.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:49293673 G>A maps to NM_178173.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr3:49293727 G>A maps to NM_178173.3 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:49294355 C>T maps to NM_178173.3 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr3:49249237 A>T maps to NM_178173.3 K9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:126142416 C>T maps to ENST00000505024 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:126132967 T>C maps to ENST00000505024 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr12:96292197 C>G maps to NM_182496.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr3:180397135 C>T maps to NM_181426.1 W11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr3:180349346 C>T maps to NM_181426.1 E636E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr3:180377514 G>A maps to NM_181426.1 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:78073332 C>G maps to NM_017950.2 S1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:78061847 G>A maps to NM_017950.2 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:78059851 G>A maps to NM_017950.2 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:78039372 C>T maps to NM_017950.2 D510D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr17:78059902 C>T maps to NM_017950.2 R779R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:78059851 G>A maps to NM_017950.2 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr17:78055841 G>A maps to NM_017950.2 K658K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr17:78073540 C>T maps to NM_017950.2 I1132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr17:78055727 C>T maps to NM_017950.2 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr17:78014038 G>A maps to NM_017950.2 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr17:78073342 G>T maps to NM_017950.2 V1066V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:94763805 C>A maps to NM_001042399.1 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:42759436 G>C maps to NM_144609.2 S121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:62523290 T>C maps to NM_138363.1 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:62533746 G>A maps to NM_138363.1 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr17:62532806 G>T maps to NM_138363.1 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr17:62504758 G>T maps to NM_138363.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr17:64049895 C>T maps to NM_145036.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:64026141 C>A did not map to a codon.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr17:64024479 A>C maps to NM_145036.3 L516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr17:64128820 T>C maps to NM_145036.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr17:61829410 C>T maps to NM_020198.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:61843453 C>A maps to NM_020198.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr17:61843339 C>A maps to NM_020198.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr17:61838272 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:128753033 C>T maps to NM_024768.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr3:128755961 T>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:191100572 G>A maps to NM_178335.2 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr3:191074895 C>T maps to NM_178335.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr3:48475191 C>T maps to NM_024661.3 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr3:113172513 G>A maps to NM_144718.3 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr3:113212123 G>A maps to NM_144718.3 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:113188078 G>C maps to NM_144718.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr12:102455052 G>A maps to NM_016053.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr17:28511682 C>G maps to NM_032141.2 S223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:28506136 A>G maps to NM_032141.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:40950642 G>A maps to NM_001040431.1 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr17:80085724 G>A maps to ENST00000445854 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr12:82750925 G>A maps to NM_014167.4 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr12:119942995 G>T maps to NM_178499.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr12:119966550 G>A maps to NM_178499.3 W454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr19:46518679 G>A maps to NM_001080402.1 K337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr12:123285715 C>T maps to NM_201435.3 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr12:123286339 C>T maps to NM_201435.3 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr12:123311014 G>A maps to NM_032573.5 *683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr12:123270331 C>T maps to NM_201435.3 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr12:123290751 G>A maps to NM_201435.3 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr12:111296515 T>G maps to NM_152591.1 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr12:111311689 C>T maps to NM_152591.1 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr12:120527844 G>T maps to NM_207311.2 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr12:120510356 C>T maps to NM_207311.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr16:3080749 G>A maps to NM_001103175.1 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr16:3085467 C>T maps to NM_001103175.1 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr12:49308296 C>T maps to NM_033124.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr12:49312056 G>C did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:56647735 G>A maps to NM_001141947.1 Q508Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:56627023 C>T maps to NM_001141947.1 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:93103297 G>C maps to NM_181645.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:93118580 C>G maps to NM_181645.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:93127692 C>A maps to NM_181645.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr11:93170883 G>A maps to NM_181645.3 *605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:48482012 G>T maps to NM_015933.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:48482024 G>A maps to NM_015933.3 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr3:48482012 G>C maps to NM_015933.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr11:32635178 A>G maps to NM_001008391.2 T895T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:32781667 A>T maps to NM_001008391.2 L41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:37319355 C>G maps to ENST00000379187 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:100614273 C>T maps to NM_019083.2 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:100608751 A>G maps to NM_019083.2 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr19:46914451 C>T maps to NM_032040.3 *539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr19:46914519 C>T maps to NM_032040.3 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr19:46915125 C>T maps to NM_032040.3 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:46914756 C>T maps to NM_032040.3 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr19:46915551 G>A maps to NM_032040.3 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr19:46915869 C>T maps to NM_032040.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:112324509 G>A maps to ENST00000447230 V880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:112356978 C>A maps to ENST00000447230 E603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr3:112326100 G>A maps to ENST00000447230 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr3:112358446 C>T maps to ENST00000447230 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr3:112357177 C>T maps to ENST00000447230 Q536Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr3:112326053 A>G maps to ENST00000447230 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:112324400 G>A maps to ENST00000447230 Q917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr11:86097119 C>G maps to NM_001156474.1 S36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr11:86098631 C>T maps to NM_001156474.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr11:86111822 G>A maps to NM_001156474.1 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:85630483 C>G maps to NM_173556.3 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:85593597 C>T maps to NM_173556.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:118881533 C>T maps to NM_198489.1 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr2:56419629 C>T maps to NM_001080433.1 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr2:56603021 A>G maps to NM_001080433.1 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:60610304 G>A maps to NM_024098.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr11:66359148 T>A maps to NM_018219.2 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:66357942 G>A maps to NM_018219.2 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:66360093 G>T maps to NM_018219.2 Y131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:66360333 C>T maps to NM_018219.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:66360120 C>T maps to NM_018219.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:66358412 C>A maps to NM_018219.2 E692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr11:66358062 C>T maps to NM_018219.2 K808K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:55615937 C>T maps to ENST00000436346 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr2:55563863 G>A maps to ENST00000436346 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr2:55576697 C>A maps to ENST00000436346 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:55559820 C>A maps to ENST00000436346 V912V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr2:55544749 C>T maps to ENST00000436346 L1184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:55523008 G>A maps to ENST00000436346 R1759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr2:55543246 C>G maps to ENST00000436346 L1250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:55559805 C>T maps to ENST00000436346 K917K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:64118967 G>A maps to NM_032251.5 E993E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr11:64108939 C>T maps to NM_032251.5 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:64119603 C>G maps to NM_032251.5 A1034A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr14:91772198 G>T maps to NM_001080414.2 T1089T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr14:91806269 G>A maps to NM_001080414.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr14:91805716 G>A maps to NM_001080414.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr14:91744439 G>A maps to NM_001080414.2 L1628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr14:91770133 C>T maps to NM_001080414.2 S1182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr14:91779999 G>A maps to NM_001080414.2 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:85396453 G>A maps to NM_152723.1 H240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr19:47761886 G>A maps to NM_015603.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr19:47773834 G>A maps to NM_015603.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr19:47769968 C>T maps to NM_015603.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr6:13799100 T>C maps to NM_001031713.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:28702104 A>G maps to NM_018318.3 *442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:124421790 G>A maps to NM_025140.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr2:118731528 G>C maps to NM_019044.4 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr19:4254470 G>A maps to NM_018074.4 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:4258351 G>A maps to NM_018074.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr19:4247148 G>T maps to NM_018074.4 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:7044014 C>T maps to NM_153376.2 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr4:7043723 C>T maps to NM_153376.2 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr4:7043386 C>A maps to NM_153376.2 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr4:7043425 C>A maps to NM_153376.2 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr5:169028326 C>T maps to NM_017785.4 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:169021604 C>T maps to NM_017785.4 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr6:31110755 G>C maps to NM_001105564.1 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr6:31110818 C>T maps to NM_001105564.1 V804V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr6:31122286 G>A maps to NM_001105564.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:31116207 C>T maps to NM_001105564.1 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr6:31125279 G>C maps to NM_001105564.1 S33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr6:31112513 G>T maps to NM_001105564.1 S706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr6:31118536 C>A maps to NM_001105564.1 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr6:31118821 C>A maps to NM_001105564.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr6:31118900 T>G did not map to a codon.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr9:36170641 C>T maps to NM_005893.2 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr9:36170284 G>A maps to NM_005893.2 Q262Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:26483792 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr4:26484817 C>T maps to NM_000730.2 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr11:6290929 C>T maps to NM_176875.2 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr17:32612838 C>A maps to NM_002986.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr17:32612856 G>T maps to NM_002986.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:34313608 G>C maps to NM_032962.4 S26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr17:32583294 C>G maps to NM_002982.3 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr9:34709656 G>A maps to NM_002989.2 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr16:57394418 C>A maps to NM_002990.4 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:8122787 G>A maps to NM_005624.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr9:34662357 G>C maps to NM_006664.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr17:32647327 C>T maps to ENST00000394620 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr7:45115442 G>A maps to NM_001029835.2 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr7:45112323 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr7:45077883 C>T maps to NM_001029835.2 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr13:37011848 C>T maps to NM_003914.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr13:37015266 C>T maps to NM_003914.3 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr13:37012778 A>G did not map to a codon.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr4:122740026 G>C maps to NM_001237.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr4:122740631 C>T maps to NM_001237.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr5:68467266 G>A maps to NM_031966.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:20781942 G>C maps to NM_182849.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr15:59406800 C>T maps to NM_004701.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:50054196 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr23:50094644 G>T did not map to a codon.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr23:50089665 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:50052840 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr23:50031855 A>G did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr23:50054339 A>T did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:50053380 G>A did not map to a codon.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr23:50051991 G>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:50053610 T>A did not map to a codon.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr23:50052074 A>G did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:50089792 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:50055610 C>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:69458748 C>T maps to NM_053056.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:69462885 C>T maps to NM_053056.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr11:69457923 C>T maps to NM_053056.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr6:41909348 G>T maps to NM_001760.3 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:41903778 G>A maps to NM_001760.3 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr6:41905012 G>C maps to NM_001760.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr15:43483713 C>G maps to NM_012142.3 S234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr8:95902766 G>C maps to NM_057749.1 S110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr8:95895083 C>A maps to NM_057749.1 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr8:95897785 C>A maps to NM_057749.1 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr16:2495527 G>T maps to NM_001761.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr16:2487193 C>T maps to NM_001761.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:2495467 G>A maps to NM_001761.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:2498933 G>A maps to NM_001761.2 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr16:2488111 G>C maps to NM_001761.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr16:2503508 C>T maps to NM_001761.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr4:78087037 C>T maps to NM_004354.2 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr4:78085518 G>A maps to NM_004354.2 K266K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr5:86690882 G>C maps to NM_001239.3 S304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr5:86690914 C>T maps to NM_001239.3 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:159682611 C>T maps to NM_024565.5 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr5:159686478 G>A maps to NM_024565.5 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr5:159680591 C>T maps to NM_024565.5 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr5:159680684 G>A maps to NM_024565.5 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:1325720 C>A maps to NM_030937.4 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:1334488 C>T maps to NM_030937.4 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:1333714 G>T maps to NM_030937.4 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:54528314 G>A maps to NM_021147.3 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr5:54528308 G>C maps to NM_021147.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:49110358 C>A maps to NM_001240.2 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr12:49087642 G>A maps to NM_001240.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr12:49093572 G>A maps to NM_001240.2 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:135712067 C>T maps to NM_058241.2 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr2:135711821 G>C maps to NM_058241.2 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr2:135711839 G>A maps to NM_058241.2 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:46245237 G>A maps to NM_001295.2 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:40831708 G>A maps to NM_016602.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:40831732 G>C maps to NM_016602.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:40831759 G>A maps to NM_016602.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:40831891 G>A maps to NM_016602.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:40831732 G>A maps to NM_016602.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr17:40831909 C>A maps to NM_016602.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:40831839 G>A maps to NM_016602.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr17:40831702 C>T maps to NM_016602.2 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:46399401 C>T maps to NM_001123041.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:46306894 C>G maps to NM_178328.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr3:46306897 C>T maps to NM_178328.1 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr3:32995474 C>T maps to NM_005508.4 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr3:46414641 C>T maps to NM_001100168.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr3:46415256 G>A maps to NM_001100168.1 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:46414962 G>A maps to NM_001100168.1 W190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr3:46414704 G>A maps to NM_001100168.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr3:46414767 T>C maps to NM_001100168.1 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr6:167550263 T>G maps to NM_004367.5 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr6:167549791 C>G maps to NM_004367.5 S25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:38711548 G>C maps to NM_001838.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr17:38711377 G>A maps to NM_001838.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr3:39373965 C>T maps to NM_005201.3 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr3:39374253 G>A maps to NM_005201.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:39374655 G>A maps to NM_005201.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr3:45943266 G>A maps to NM_031200.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr3:132319325 C>T maps to NM_178445.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr4:139966384 G>A maps to NM_012118.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr4:139964270 C>G maps to NM_012118.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr11:66361123 G>C maps to NM_005125.1 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr1:156281972 C>G maps to NM_005998.4 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:156280782 C>T maps to NM_005998.4 Q453Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:156281921 A>G maps to NM_005998.4 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:156280932 C>T maps to NM_005998.4 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr2:62103249 G>A maps to NM_006430.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr2:62104159 C>T maps to NM_006430.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr5:10254300 A>C maps to NM_012073.3 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr5:10262688 G>T maps to NM_012073.3 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:33259397 G>C maps to NM_006584.3 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr17:33288310 C>T maps to NM_006584.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr2:73466823 C>T maps to NM_006429.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:73466850 C>T maps to NM_006429.3 C29C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:73474900 G>A maps to NM_006429.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr2:73476291 G>A maps to NM_006429.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr21:30435689 A>G maps to NM_006585.2 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr21:30437348 G>A maps to NM_006585.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr21:30439220 G>A maps to NM_006585.2 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr22:17072819 C>T maps to NM_014406.4 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr22:17072000 C>T maps to NM_014406.4 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr22:17073278 G>A maps to NM_014406.4 H54H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr22:17071844 G>A maps to NM_014406.4 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr22:17072543 G>A maps to NM_014406.4 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr1:117552556 C>A maps to NM_004258.3 C43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:117554560 C>T maps to NM_004258.3 Q272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr1:117568226 C>A maps to NM_004258.3 S842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:117576548 C>T maps to NM_004258.3 F964F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:74407260 C>G maps to NM_133493.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr6:74473392 C>G maps to NM_133493.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr6:74524748 C>T maps to NM_133493.3 R1272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr6:74472501 G>A maps to NM_133493.3 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr6:74468730 A>G maps to NM_133493.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr6:74497084 C>T maps to NM_133493.3 I822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr6:74472148 A>T maps to NM_133493.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:74477933 C>T maps to NM_133493.3 Q552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr5:140011717 G>T maps to NM_001174105.1 S284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:837263 C>T maps to NM_139030.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr12:7656274 G>A maps to NM_004244.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr12:7635262 G>A maps to NM_004244.4 R1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:7639409 C>G did not map to a codon.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr12:7647884 C>G maps to NM_004244.4 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr12:7651506 C>T maps to NM_004244.4 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr12:7640063 C>T maps to NM_004244.4 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr12:7551148 C>T maps to ENST00000416109 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr12:7556185 A>G maps to ENST00000416109 D461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:7527245 C>G maps to ENST00000416109 L1077L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr12:7528191 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr12:7526236 C>T did not map to a codon.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr12:7528478 C>A maps to ENST00000416109 E845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr12:7559341 C>T maps to ENST00000416109 W301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:7526063 G>A maps to ENST00000416109 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T4-01A-11D-A391-08 chr12:7531610 C>T maps to ENST00000416109 A788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr12:7550875 C>G maps to ENST00000416109 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr12:7548850 G>A maps to ENST00000416109 I640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr19:43865690 C>T maps to NM_020406.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr19:43859825 G>A maps to NM_020406.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr5:66479989 C>T maps to NM_005582.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr16:28946783 G>A maps to NM_001178098.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:28948443 C>T maps to NM_001178098.1 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr16:28947483 G>C maps to NM_001178098.1 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr1:158224901 C>A maps to NM_001763.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr1:158224515 C>T maps to NM_001763.2 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr1:158227280 G>A maps to NM_001763.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:158301204 C>T maps to NM_001764.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:158300751 C>T maps to NM_001764.2 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr1:158299223 C>T maps to NM_001764.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:158261185 G>A maps to NM_001765.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:158262506 G>A maps to NM_001765.2 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr1:158152731 C>A maps to NM_001766.3 C224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr1:158152902 G>A maps to NM_001766.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr1:158151867 G>A maps to NM_001766.3 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr1:158325144 C>T maps to NM_030893.3 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:158326597 C>G maps to NM_030893.3 S360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:158326605 C>T maps to NM_030893.3 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:158325249 C>G maps to NM_030893.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:117297378 C>G maps to NM_001767.3 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:112059795 G>A maps to NM_001004196.2 W45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr3:112546430 C>G maps to NM_001008784.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:112546397 C>T maps to NM_001008784.2 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr3:112546280 C>A maps to NM_001008784.2 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:71060999 C>T maps to NM_015717.3 E114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr2:71060099 C>T maps to NM_015717.3 W216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr2:71058237 T>C maps to NM_015717.3 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr19:7810764 C>A maps to NM_021155.3 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr19:7807987 G>A maps to NM_021155.3 C384C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr19:7809002 G>A maps to NM_021155.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr19:7808071 G>A maps to NM_021155.3 C356C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr19:35823771 G>C maps to NM_001771.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:35823513 C>T maps to NM_001771.3 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr19:35831920 G>T maps to NM_001771.3 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:167408586 G>C maps to NM_198053.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:167409969 G>T maps to NM_198053.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:66082599 G>A maps to NM_020404.2 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:66082773 G>A maps to NM_020404.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr11:66083454 G>A maps to NM_020404.2 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr11:66083094 C>T maps to NM_020404.2 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr12:6554302 C>A maps to NM_001242.4 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr15:73992051 C>T maps to NM_001024736.1 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr2:204591440 C>T maps to NM_006139.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr6:47544788 G>T maps to NM_012120.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:47512408 G>A maps to NM_012120.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr6:47512340 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:47591932 G>A maps to NM_012120.2 E630E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr16:30364573 C>G maps to NM_006110.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr16:30365990 C>T maps to NM_006110.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr16:30365993 C>T maps to NM_006110.2 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr16:30365947 C>A maps to NM_006110.2 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr16:30365607 C>T maps to NM_006110.2 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BS-01A-21D-A26M-08 chr16:30365640 C>T maps to NM_006110.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:72462871 C>G maps to NM_007261.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr17:72613535 G>A maps to ENST00000426295 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr17:72691300 G>A maps to ENST00000412086 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr17:72699196 C>T maps to ENST00000412086 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr17:41926217 G>C maps to NM_145273.3 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr19:51742941 G>A maps to NM_001772.3 *365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr19:51729083 C>T maps to NM_001772.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:208062849 C>T maps to NM_001025109.1 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr1:208072506 A>G maps to NM_001025109.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:208072531 G>C maps to NM_001025109.1 S101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr1:208072571 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:49840235 C>T maps to NM_001774.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:49842009 G>A maps to NM_001774.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr19:49838984 G>C maps to NM_001774.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr4:15780141 C>T maps to NM_001775.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:118213298 A>G maps to NM_000732.4 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr19:45912503 G>A maps to ENST00000423698 K428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:45912500 G>A maps to ENST00000423698 K427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:118221327 C>T maps to NM_000073.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr11:118220499 C>A maps to NM_000073.2 S41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr11:118221393 G>A maps to NM_000073.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:6926359 G>T maps to NM_000616.4 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr12:6923320 G>A maps to NM_000616.4 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr20:44751804 C>G maps to NM_001250.4 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr20:44756799 C>T maps to NM_001250.4 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr20:44756828 C>A maps to NM_001250.4 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr23:135732523 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:135741328 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:35226110 G>A maps to NM_000610.3 Q402Q. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-A3WW-01A-22D-A23M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:207966934 G>T maps to ENST00000441839 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:207963645 C>G maps to NM_002389.4 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr1:207934592 G>C did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr3:107798973 G>A maps to NM_001777.3 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:107779598 G>A maps to NM_001777.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:160681498 G>A maps to NM_001778.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:160681498 G>A maps to NM_001778.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr11:60885819 T>C maps to NM_014207.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr11:60886391 C>T maps to NM_014207.3 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr11:60893301 G>A maps to NM_014207.3 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:60889101 G>A maps to NM_014207.3 Q275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:111436953 C>T maps to NM_000560.3 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:111437633 C>G maps to NM_000560.3 S127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:207510110 C>G maps to NM_001114752.1 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:117078794 G>C maps to NM_001779.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr1:117078650 A>T maps to NM_001779.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr1:157803165 C>T maps to NM_005894.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr11:60780955 C>T maps to NM_006725.3 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr11:60777200 G>A maps to NM_006725.3 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:60781006 C>T maps to NM_006725.3 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr11:60785402 C>T maps to NM_006725.3 P585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr11:60781469 C>T maps to NM_006725.3 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr12:9913401 A>G maps to NM_001781.2 N5N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr9:35612926 G>C maps to NM_001782.2 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr5:149782801 G>A maps to NM_001025159.1 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr19:42381453 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr19:42383360 T>G did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:62007162 G>A maps to NM_001039933.1 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr11:2417886 C>T maps to NM_004356.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:160520799 G>T maps to NM_001184879.1 Y279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr3:121822488 G>C maps to NM_175862.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:121825276 G>A maps to NM_175862.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr2:87016548 C>T maps to ENST00000456996 T215T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-E7-A85H-01A-11D-A34U-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr12:6344474 G>A maps to NM_001769.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr12:6334629 C>G maps to NM_001769.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr12:6344684 C>G maps to NM_001769.2 S164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr20:23065233 G>C maps to NM_012072.3 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr20:23066061 G>T maps to NM_012072.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr20:23066304 A>G maps to NM_012072.3 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr3:111264031 G>A maps to NM_198196.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:14516630 C>T maps to NM_078481.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:14508890 C>T maps to NM_078481.2 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr19:14517986 C>G maps to NM_078481.2 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr19:14513430 C>G maps to NM_078481.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr23:2658836 G>C did not map to a codon.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr23:2658836 G>C did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:149963916 G>T did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr23:149944695 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:20944967 C>T maps to NM_001785.2 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:20945010 G>T maps to NM_001785.2 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr15:43022925 G>A maps to NM_138477.2 R682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr15:43020878 G>A maps to NM_138477.2 H925H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr15:43025296 G>A maps to NM_138477.2 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:43018339 C>A maps to NM_138477.2 E1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr15:43023131 G>A maps to NM_138477.2 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr10:12259406 C>T maps to NM_006023.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr10:12252320 G>A maps to NM_006023.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:100920980 C>T maps to NM_033312.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr1:100949902 C>T maps to NM_033312.2 R345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr9:99381612 G>C maps to NM_033331.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr13:115008756 C>T maps to NM_003903.3 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr1:43826469 G>A maps to NM_001255.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr1:43825270 G>T maps to NM_001255.2 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr5:54410096 C>T maps to NM_001170402.1 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:54436169 G>C maps to NM_001170402.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr5:54420850 G>C maps to NM_001170402.1 S332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr5:54442573 T>C maps to NM_001170402.1 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr5:137525546 G>A maps to NM_004661.3 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr3:48226162 C>T maps to NM_001789.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr20:3781634 G>A maps to NM_021873.2 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr20:3785541 C>G maps to NM_021873.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:3783804 G>A maps to NM_021873.2 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:137622208 G>A maps to NM_001790.3 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:137622920 C>T maps to NM_001790.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr5:137654925 C>T maps to NM_001790.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr5:137654925 C>T maps to NM_001790.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:137622193 G>A maps to NM_001790.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr17:45234400 A>G maps to NM_001114091.1 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr17:45216197 C>T maps to NM_001114091.1 E543E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:45229302 C>G did not map to a codon.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr17:45219269 C>T maps to NM_001114091.1 W506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr17:45247376 C>A maps to NM_001114091.1 G95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:541368 G>A maps to NM_004359.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:10503961 G>A maps to NM_007065.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr6:110522828 C>T maps to NM_015891.2 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:22416521 C>T maps to NM_044472.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:227227862 C>G maps to ENST00000366766 V1056V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr1:227333351 A>G maps to ENST00000366766 H327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:227316870 G>A maps to ENST00000366766 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:227288847 G>T maps to ENST00000366766 I698I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr1:227307534 C>T maps to ENST00000366766 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:227259909 C>T maps to ENST00000366766 K942K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:227441766 C>A maps to ENST00000366766 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:227219119 C>G maps to ENST00000366766 L1218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr14:103442106 G>C maps to NM_006035.3 S474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr14:103442093 G>A maps to NM_006035.3 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:103406201 G>A maps to NM_006035.3 F1558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr14:103442093 G>C maps to NM_006035.3 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr14:103465927 G>A maps to NM_006035.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr14:103410591 C>A maps to NM_006035.3 V1348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr14:103438300 G>A maps to NM_006035.3 D613D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr14:103436490 G>C maps to NM_006035.3 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr14:103412823 G>A maps to NM_006035.3 I1243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr14:103412916 G>C maps to NM_006035.3 L1212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr14:103410591 C>A maps to NM_006035.3 V1348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:64599968 G>A maps to NM_017525.2 F1006F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr11:64595071 G>A maps to NM_017525.2 L1359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:64597048 G>T maps to NM_017525.2 L1287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr11:64597297 G>A maps to NM_017525.2 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:65088416 C>T maps to NM_006779.2 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr2:37873427 C>T maps to NM_006449.3 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr2:37873445 G>A maps to NM_006449.3 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr2:37873475 G>A maps to NM_006449.3 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr17:71281970 G>A maps to NM_012121.4 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr17:71281695 G>C maps to NM_012121.4 S315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:71282071 G>A maps to NM_012121.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:71282141 C>A maps to NM_012121.4 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:19506421 C>A maps to NM_001178010.1 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr22:19504099 G>A maps to NM_001178010.1 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr22:19492956 G>A maps to NM_001178010.1 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr22:19481851 G>A maps to NM_001178010.1 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr6:44387199 C>T maps to NM_001253.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:38445696 C>T maps to NM_001254.3 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr17:38447571 G>C maps to NM_001254.3 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr17:38457717 A>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:91978755 G>A maps to NM_001134420.1 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:193117043 A>G maps to NM_024529.4 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr8:25343312 C>G maps to ENST00000434814 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr8:25341527 G>A maps to ENST00000434814 K390K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr12:6958993 C>T maps to NM_031299.4 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr14:105478086 G>C maps to NM_145701.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr11:64847001 G>A maps to ENST00000404147 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr2:174223510 G>A maps to NM_031942.4 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:174231088 C>T maps to NM_031942.4 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:174229683 G>A maps to NM_031942.4 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr2:174228054 A>G maps to NM_031942.4 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr7:21945944 C>A maps to NM_018719.4 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:38161615 G>A maps to NM_018101.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:38172732 C>G maps to NM_018101.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:38174036 G>C maps to NM_018101.2 *281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr3:45153728 G>T maps to NM_022842.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr1:54605291 G>A maps to NM_201546.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:54607035 C>T maps to NM_201546.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr1:54610247 G>A maps to NM_201546.2 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:54606978 C>T maps to NM_201546.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr16:68846153 C>T maps to NM_004360.3 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:68857306 G>T maps to NM_004360.3 E648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr16:68844152 G>A maps to NM_004360.3 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr16:68846079 C>T maps to NM_004360.3 Q351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:68856093 G>A maps to NM_004360.3 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr16:68842437 G>T maps to NM_004360.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr16:68842715 G>T maps to NM_004360.3 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr16:68856019 C>T maps to NM_004360.3 Q610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr16:68849603 C>T maps to NM_004360.3 Q503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr16:68835595 C>T maps to NM_004360.3 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:24535866 T>C maps to NM_006727.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:24593506 C>T maps to NM_006727.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr5:24511623 C>T did not map to a codon.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr5:24537645 G>C maps to NM_006727.3 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr5:24488011 G>A maps to NM_006727.3 D709D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr5:24593406 C>A maps to NM_006727.3 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr16:64984855 G>A maps to NM_001797.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr16:65038571 G>A maps to NM_001797.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr16:65022074 C>T maps to NM_001797.2 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr16:64984874 C>T maps to NM_001797.2 Q563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr16:65032528 A>G maps to NM_001797.2 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr16:64981895 C>T maps to NM_001797.2 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr16:64981661 A>C maps to NM_001797.2 Y745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T4-01A-11D-A391-08 chr16:65016141 G>A maps to NM_001797.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr5:21842318 G>A maps to NM_004061.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:83817066 C>T maps to ENST00000268613 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr16:82891975 C>T maps to ENST00000268613 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr16:83781739 T>C maps to ENST00000268613 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr16:83704468 C>T maps to ENST00000268613 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr16:89258802 C>T maps to NM_004933.2 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr16:89261394 G>A maps to NM_004933.2 E759E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:89256661 T>C maps to NM_004933.2 Y330Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:89245822 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:66948238 G>A maps to NM_004062.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr16:66945115 G>C maps to NM_004062.2 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:66945866 G>A maps to NM_004062.2 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr16:66946168 C>T maps to NM_004062.2 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:66945205 G>A maps to NM_004062.2 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr8:95186396 G>A maps to NM_001144663.1 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr8:95186218 G>A maps to NM_001144663.1 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr8:95164111 C>A maps to NM_001144663.1 E594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr8:95178091 G>C maps to NM_001144663.1 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr8:95158243 A>G maps to NM_001144663.1 D693D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr8:95186186 A>T maps to NM_001144663.1 Y207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr8:95164211 C>T maps to NM_001144663.1 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr5:19544029 G>A maps to NM_004934.3 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr5:19503203 G>A maps to NM_004934.3 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:19473423 G>A maps to NM_004934.3 Q762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr5:19839038 C>A maps to NM_004934.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr5:19839053 C>T maps to NM_004934.3 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr5:19721462 A>G maps to NM_004934.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr18:64211461 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr18:64221672 G>T maps to NM_021153.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr18:64178817 G>A maps to NM_021153.2 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr18:25593676 C>T maps to NM_001792.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:25532173 G>A maps to NM_001792.3 N888N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr18:25532200 A>C maps to NM_001792.3 G879G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr18:25591884 C>T maps to NM_001792.3 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr18:59166705 C>T maps to NM_031891.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr18:59166462 C>A maps to NM_031891.2 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr20:44869806 C>G maps to NM_021248.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:44803690 G>A maps to NM_021248.1 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr20:44869806 C>G maps to NM_021248.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr20:44815311 G>A maps to NM_021248.1 D526D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:44856219 C>T maps to NM_021248.1 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr20:44815225 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr10:73545470 G>T maps to ENST00000398860 P1937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr10:73461909 G>A maps to ENST00000398860 E848E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:73437305 G>A maps to ENST00000398860 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:73472563 C>A maps to ENST00000398860 I1126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr10:73326686 C>T maps to ENST00000398860 N211N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr10:73569730 C>T maps to ENST00000398860 I2964I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr10:73462366 C>G maps to ENST00000398860 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr10:73437254 C>T maps to ENST00000398860 A524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr10:73326644 G>A maps to ENST00000398860 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:23524349 G>A maps to NM_022478.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr14:23522882 G>A maps to NM_022478.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr20:58545231 C>T maps to NM_177980.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr20:58545165 C>T maps to NM_177980.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:68721628 C>T maps to NM_001793.4 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:68721568 C>T maps to NM_001793.4 H575H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr16:68712083 C>G maps to NM_001793.4 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr16:68716311 C>T maps to NM_001793.4 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr16:68716272 C>T maps to NM_001793.4 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr20:60499396 C>G maps to NM_001794.2 S545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr20:60508097 G>A maps to NM_001794.2 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr20:60511868 C>T maps to NM_001794.2 S873S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr20:60509142 G>T maps to NM_001794.2 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr20:60427877 C>T maps to NM_001794.2 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:66420776 C>A maps to NM_001795.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr16:66426055 C>T maps to NM_001795.3 Y329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:66426235 G>C maps to NM_001795.3 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr16:66434797 C>T maps to NM_001795.3 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr16:66437030 G>T maps to NM_001795.3 E772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr16:66420932 G>A maps to NM_001795.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:31302359 C>T maps to NM_004932.2 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr5:31267660 G>A maps to NM_004932.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr5:31317572 C>G maps to NM_004932.2 S535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr18:63511109 C>T maps to NM_004361.2 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr18:63492067 G>A did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr18:63526159 G>C did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr16:61761011 C>A maps to NM_001796.2 G508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr16:61935121 C>A maps to NM_001796.2 G170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr16:61854889 T>A maps to NM_001796.2 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr16:61858916 C>T maps to NM_001796.2 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr16:61687544 G>C maps to NM_001796.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr16:61689437 G>A maps to NM_001796.2 V614V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:61689578 C>T maps to NM_001796.2 Q567Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr5:26886093 G>A maps to NM_016279.3 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr5:26881388 C>A maps to NM_016279.3 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr10:85973932 C>T maps to NM_033100.2 V712V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:176019723 C>T maps to NM_001171976.1 S1245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr5:176005566 C>T maps to NM_001171976.1 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr5:176012979 C>T maps to NM_001171976.1 D920D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr5:176011808 G>T maps to NM_001171976.1 E843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr5:176011561 G>T maps to NM_001171976.1 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr7:105615294 G>T maps to NM_152750.4 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr7:105662836 G>A maps to NM_152750.4 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr7:105672956 C>T maps to NM_152750.4 V824V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:105655577 G>T maps to NM_152750.4 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:105645020 G>T maps to NM_152750.4 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr11:618727 G>A maps to NM_021924.4 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr11:619482 G>A maps to NM_021924.4 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:618013 G>A maps to NM_021924.4 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr11:617953 C>T maps to NM_021924.4 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:620144 G>A maps to NM_021924.4 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr10:62553723 G>A maps to NM_001786.4 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr16:89759687 G>A maps to NM_052988.4 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr16:89757911 C>T maps to NM_052988.4 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:89759836 C>A maps to NM_052988.4 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:1635766 C>G maps to NM_024011.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:1634991 G>A maps to NM_024011.2 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr1:1638913 G>A maps to NM_024011.2 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:1635006 G>C maps to NM_024011.2 V656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:1636405 G>A maps to NM_024011.2 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:1572547 C>G maps to ENST00000401097 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr1:1572052 C>T maps to ENST00000401097 K634K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr17:37627780 C>T maps to NM_016507.2 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:37649081 T>C maps to NM_016507.2 I729I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr17:37687082 C>T maps to NM_016507.2 S1329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:37687208 G>A maps to NM_016507.2 V1371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:37619090 C>A maps to NM_016507.2 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr17:37646960 C>T maps to NM_016507.2 Q695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr7:40102456 G>A maps to NM_003718.4 W878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr7:40133796 C>T maps to NM_003718.4 R1253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:40132606 G>A maps to NM_003718.4 S1153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr7:40027398 G>A maps to NM_003718.4 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr7:40102699 G>A did not map to a codon.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr7:40085527 C>A maps to NM_003718.4 S816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr7:90356125 G>C maps to NM_012395.2 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr2:202698638 G>C maps to ENST00000450471 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:202755539 C>T maps to ENST00000450471 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:202698645 C>T maps to ENST00000450471 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:47083089 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:47083091 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:47083914 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:47082967 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr23:47083821 G>T did not map to a codon.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr23:47083021 C>A did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr23:47083837 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:47085745 C>G did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:47086255 C>G did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:205492698 C>T maps to NM_212503.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:205498222 C>T maps to NM_212503.2 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:205492647 G>A maps to NM_212503.2 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr1:205495907 T>C maps to NM_212503.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr1:205498156 C>A maps to NM_212503.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:205497028 G>C maps to NM_212503.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr1:205496926 C>T maps to NM_212503.2 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr6:110943359 G>A maps to NM_015076.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:111136324 G>A maps to NM_015076.3 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:111136210 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr9:90588986 C>G maps to NM_178432.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr17:73999334 T>C maps to NM_001258.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr12:58145446 C>T maps to NM_000075.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr12:58143280 G>A maps to NM_000075.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr7:150753714 C>T maps to NM_004935.3 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr7:150754179 C>T maps to NM_004935.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr7:150751355 T>G maps to NM_004935.3 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr17:30815243 C>T maps to NM_003885.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:30814981 C>A maps to NM_003885.2 S115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:30814826 G>A maps to NM_003885.2 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:30814991 G>A maps to NM_003885.2 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:219825384 C>G maps to NM_003936.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr20:31948264 G>T maps to ENST00000357886 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr20:31962019 T>G did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr20:31954742 G>A maps to ENST00000357886 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr20:31973473 C>T maps to ENST00000357886 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr20:31961943 A>T maps to ENST00000357886 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr9:123151528 G>A maps to NM_018249.4 S1889S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr9:123169488 G>A maps to NM_018249.4 F1588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:123202076 C>A maps to NM_018249.4 E1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr17:46052585 G>A maps to NM_176096.1 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr17:46053300 G>A maps to NM_176096.1 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr17:46058603 G>C maps to NM_176096.1 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr7:92300795 G>A maps to NM_001145306.1 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr7:92462442 C>T maps to NM_001145306.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr7:92462442 C>T maps to NM_001145306.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:68548243 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr13:26828879 C>T maps to NM_001260.1 H34H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr13:26975742 C>T maps to NM_001260.1 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:21065356 G>A maps to NM_017774.3 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr6:20546670 A>G maps to NM_017774.3 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:20758833 G>A maps to NM_017774.3 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr6:20781487 C>T maps to NM_017774.3 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr14:50807748 C>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr4:76529000 C>T maps to ENST00000307465 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr5:133685983 C>T maps to NM_001113575.1 W165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:18643278 C>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:18622975 C>T did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr23:18622500 C>A did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr23:18622520 A>G did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:18593486 C>G did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:18616647 C>G did not map to a codon.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr6:36652023 G>A maps to ENST00000448526 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr6:36651905 C>T maps to ENST00000448526 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr6:36651905 C>T maps to ENST00000448526 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr6:36652019 C>T maps to ENST00000448526 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr6:36651905 C>T maps to ENST00000448526 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr6:36652023 G>A maps to ENST00000448526 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:36651967 G>A maps to ENST00000448526 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:12871769 C>T maps to NM_004064.3 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr12:12871793 G>T maps to NM_004064.3 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr9:21974791 G>T maps to NM_001195132.1 S12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr9:21971208 T>A did not map to a codon.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr9:21971207 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr4:184367944 C>T maps to NM_017632.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr4:184367239 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:133747453 G>C maps to NM_080656.2 S31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr11:125891383 G>C maps to ENST00000392693 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr11:125831778 C>T maps to ENST00000392693 V1157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:125853779 C>T maps to ENST00000392693 Q994Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr23:139865961 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr23:139866322 G>A did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr23:139866479 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr23:139866321 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr23:139866026 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr23:139865949 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr17:73000132 C>T maps to NM_014603.2 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr17:72997467 C>T maps to NM_014603.2 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T4-01A-11D-A391-08 chr17:73000111 C>T maps to NM_014603.2 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:15522809 G>C maps to ENST00000261644 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr17:15516017 C>T maps to ENST00000455584 T697T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:15496727 G>A maps to ENST00000261644 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr20:5170442 G>C maps to NM_003818.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr20:5170799 C>T maps to NM_003818.2 Q420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr6:31083987 A>G maps to NM_001264.4 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr6:31084611 G>A maps to NM_001264.4 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr6:31083951 G>A maps to NM_001264.4 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:88870298 C>T maps to NM_030928.3 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr16:88871853 G>A maps to NM_030928.3 E165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr16:88872212 C>A maps to NM_030928.3 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr13:28542656 G>T maps to NM_001265.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:4943830 C>T maps to ENST00000328908 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr16:80718570 G>A maps to NM_152342.2 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr16:80718993 C>T maps to NM_152342.2 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr16:80718549 C>T maps to NM_152342.2 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr19:43016631 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:43026091 G>A maps to NM_001712.4 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:43026085 C>T maps to NM_001712.4 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr19:43031532 C>T maps to NM_001712.4 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr19:43025626 A>G maps to NM_001712.4 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:43026174 G>A maps to NM_001712.4 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr19:51984906 C>T maps to NM_001080405.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:51981817 G>A maps to NM_001080405.1 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr19:45179639 C>T maps to NM_020219.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:45015146 G>A maps to NM_001102597.1 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:42092191 G>A did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:42132179 T>A maps to NM_001817.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr19:42224902 C>A maps to NM_004363.2 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:42222296 C>A maps to NM_004363.2 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:42219614 A>G maps to NM_004363.2 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:42225091 C>G maps to NM_004363.2 V674V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr19:42260766 G>A maps to NM_002483.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr19:42265343 C>T maps to NM_002483.4 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr19:42191090 C>T maps to NM_006890.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr19:33792336 C>T maps to NM_004364.3 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:33792438 G>T maps to NM_004364.3 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr20:48808575 G>T maps to NM_005194.2 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr14:23588120 C>T maps to NM_001805.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr14:23586910 G>T maps to NM_001805.2 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr14:23586839 C>T maps to NM_001805.2 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr14:23586977 G>C maps to NM_001805.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr19:33870498 C>G maps to NM_001806.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr2:37455162 C>G maps to NM_005760.2 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr2:37443322 C>T maps to NM_005760.2 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr22:17690353 T>A maps to NM_017424.2 K72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr22:17976470 C>T maps to ENST00000400579 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr22:17976488 C>T maps to ENST00000400579 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr22:17976512 G>C maps to ENST00000400579 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr22:17622073 C>T maps to NM_033070.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:17619240 G>A maps to NM_033070.2 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:17624009 C>T maps to NM_033070.2 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr22:17600372 G>A maps to NM_031890.3 Q549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr22:17601327 C>T maps to NM_031890.3 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr9:135940562 C>T maps to NM_001807.3 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr9:135947124 C>T maps to NM_001807.3 Q749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:135945949 C>T maps to NM_001807.3 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr9:135940496 C>G maps to NM_001807.3 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr1:15789242 C>T maps to ENST00000375924 Y118Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr1:15813856 G>A maps to ENST00000442979 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:15809800 C>T maps to ENST00000442979 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:15813790 T>A maps to ENST00000442979 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:22333439 C>A maps to NM_005747.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:22333487 C>T maps to NM_005747.4 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:22307566 C>T maps to NM_007352.2 Y88Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr1:22304934 C>T maps to NM_007352.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr1:22307602 C>T maps to NM_007352.2 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:22303558 C>T maps to NM_007352.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr1:22313043 C>G maps to NM_007352.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr1:22310251 C>G maps to NM_007352.2 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr11:47510397 G>A maps to NM_001172639.1 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr11:47493802 C>T maps to NM_001172639.1 K506K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr11:47498978 T>C did not map to a codon.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr10:11207489 C>G maps to NM_006561.3 S39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr10:11312645 C>T maps to NM_006561.3 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr10:11207532 G>A maps to NM_006561.3 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr10:11259436 G>A maps to NM_006561.3 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr10:11363176 G>A maps to NM_006561.3 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr1:151677543 C>T maps to NM_007185.4 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr18:34839144 G>A maps to NM_020180.3 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr18:34839144 G>A maps to NM_020180.3 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr18:34833887 G>A maps to NM_020180.3 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr18:34854294 G>A maps to NM_020180.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:3290310 C>T maps to NM_021938.3 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:3284909 G>C maps to NM_021938.3 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr15:72581515 G>A maps to NM_052840.4 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr15:72608197 C>T maps to NM_052840.4 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr22:46931750 G>T maps to NM_014246.1 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr22:46859964 G>A maps to NM_014246.1 F1274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr22:46929663 G>C maps to NM_014246.1 S1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr22:46792542 G>A maps to NM_014246.1 C1934C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr22:46792605 C>A maps to NM_014246.1 L1913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr22:46932098 C>T maps to NM_014246.1 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr22:46931027 C>G maps to NM_014246.1 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr22:46859619 G>T maps to NM_014246.1 C1389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr22:46859880 G>A maps to NM_014246.1 F1302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:46759984 C>T maps to NM_014246.1 K2981K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr22:46787590 G>A maps to NM_014246.1 I2029I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr22:46805003 C>G maps to NM_014246.1 L1705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr22:46805772 G>A maps to NM_014246.1 C1646C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr22:46794519 G>A maps to NM_014246.1 I1809I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:109793957 C>G maps to NM_001408.2 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:109795715 C>T maps to NM_001408.2 S1005S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr1:109794479 G>A maps to NM_001408.2 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr1:109805451 G>C maps to NM_001408.2 L1523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr1:109806317 C>T maps to NM_001408.2 L1640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:109805872 C>T maps to NM_001408.2 G1606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr1:109806338 C>T maps to NM_001408.2 R1647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr1:109795842 C>T maps to NM_001408.2 R1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:109814235 C>T maps to NM_001408.2 F2606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr1:109815500 G>A maps to NM_001408.2 Q2730Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:109794398 T>C maps to NM_001408.2 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr3:48686552 C>A did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr3:48691104 G>A maps to NM_001407.2 Q1799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:48687964 G>T maps to NM_001407.2 P2140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr3:48698816 C>T maps to NM_001407.2 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr3:48675651 C>A maps to NM_001407.2 E3309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr3:48694482 G>A maps to NM_001407.2 S1349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:48679296 G>A maps to NM_001407.2 L2937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:48698804 C>G maps to NM_001407.2 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:48678957 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr3:48697835 C>A maps to NM_001407.2 V744V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr3:48699137 C>T maps to NM_001407.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr3:48685348 G>A maps to NM_001407.2 R2352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:48679389 G>C maps to NM_001407.2 L2906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:48699980 G>A maps to NM_001407.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:27016086 C>G maps to NM_001809.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr2:27016062 C>T maps to NM_001809.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:3765426 C>T maps to NM_001810.5 Q568Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr16:90038222 C>T maps to NM_145039.3 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr4:104103930 A>C maps to NM_001813.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr4:104061056 A>G maps to NM_001813.2 L2031L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr4:104070086 C>A maps to NM_001813.2 E1253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:104115598 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:104082408 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr4:104082503 C>G maps to NM_001813.2 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr4:104079968 C>T maps to NM_001813.2 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:104066983 A>T did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr4:104066236 C>T maps to NM_001813.2 L1609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr4:104102525 C>A maps to NM_001813.2 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:214805896 G>A maps to NM_016343.3 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:214814563 C>T maps to NM_016343.3 I961I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:214815001 G>A maps to NM_016343.3 Q1107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:214826226 C>A maps to NM_016343.3 L2739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:214816372 G>A maps to NM_016343.3 E1564E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:214813277 C>T maps to NM_016343.3 Q533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr1:214819611 C>G maps to NM_016343.3 L2233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:214832304 G>A maps to NM_016343.3 L3025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr1:214820019 A>G maps to NM_016343.3 L2369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr1:214814729 C>T maps to NM_016343.3 Q1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:214828690 G>A maps to NM_016343.3 E2810E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:214817933 C>G maps to NM_016343.3 S1674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr1:214795554 G>A maps to NM_016343.3 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr1:214837061 C>T maps to NM_016343.3 V3090V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr23:100417902 C>T did not map to a codon.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr23:100364524 C>G did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr23:100382568 C>G did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:100402960 G>C did not map to a codon.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr23:100385037 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr23:100402945 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr23:100402772 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:25458347 C>T maps to NM_018451.3 T1218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr13:25457365 C>T maps to NM_018451.3 R1322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr13:25479558 A>G maps to NM_018451.3 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr5:64824347 G>C maps to NM_022145.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:173776539 G>C maps to NM_001127181.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr1:173772178 G>A maps to NM_001127181.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr1:173772367 A>G maps to NM_001127181.2 H278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr22:42341966 C>T maps to NM_024053.3 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:81053749 C>T maps to NM_001100624.1 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:81056427 G>A maps to NM_018455.4 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:25037315 G>A maps to NM_024322.2 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMJ-01A-11D-A42E-08 chr2:25038558 C>T maps to NM_024322.2 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr2:25022646 C>G maps to NM_024322.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr2:25039531 C>T maps to NM_024322.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr16:67862414 C>T maps to NM_025082.3 K508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:16251980 C>T maps to NM_181716.2 K176K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr9:123921141 C>T maps to NM_007018.4 Q1592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:123924224 G>A maps to NM_007018.4 E1727E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr9:123907176 C>T maps to NM_007018.4 L1036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr9:123911079 C>G maps to NM_007018.4 S1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr9:123852673 G>A maps to NM_007018.4 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr9:123907176 C>T maps to NM_007018.4 L1036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr9:123917004 C>T maps to NM_007018.4 F1393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr9:123924242 G>A maps to NM_007018.4 V1733V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr4:56885581 G>T maps to NM_025009.3 E1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:56878112 C>T maps to NM_025009.3 R922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr4:56883882 G>T maps to NM_025009.3 E958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr15:49076284 C>T maps to NM_001194998.1 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr15:49031132 G>A maps to NM_001194998.1 L1482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr15:49031132 G>A maps to NM_001194998.1 L1482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr15:49076265 G>A maps to NM_001194998.1 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr15:49083543 G>A maps to NM_001194998.1 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr11:117232654 C>T maps to NM_014956.4 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr11:117253628 C>T maps to NM_014956.4 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr11:117241906 C>T maps to NM_014956.4 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:243328907 G>C maps to NM_014812.2 S785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr1:243388524 G>A maps to NM_014812.2 R20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr1:243349593 G>C maps to NM_014812.2 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr18:13059090 C>G maps to NM_032142.3 S1423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr18:13068355 A>G did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr18:13057682 G>A maps to NM_032142.3 W1403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr18:13059226 G>C maps to NM_032142.3 S1468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr18:13069783 C>T maps to NM_032142.3 L1701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr18:13092376 A>G maps to NM_032142.3 V2035V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr18:13059190 C>T maps to NM_032142.3 F1456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr18:13114181 C>T maps to NM_032142.3 L2407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr18:13071094 C>T maps to NM_032142.3 G1744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr18:13087567 C>A maps to NM_032142.3 I1972I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr18:13049485 C>G maps to NM_032142.3 S899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr18:13087597 T>A maps to NM_032142.3 T1982T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:34065848 G>T maps to NM_007186.3 E673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:34065902 G>T maps to NM_007186.3 E691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr20:34091584 G>A maps to NM_007186.3 L1796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr20:34054004 G>A maps to NM_007186.3 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr20:34082421 G>A maps to NM_007186.3 E1035E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr20:34090366 G>C maps to NM_007186.3 L1390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr20:34063378 C>T maps to NM_007186.3 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr20:34057720 C>G maps to NM_007186.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr20:34053884 G>C maps to NM_007186.3 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr20:34054807 G>A maps to NM_007186.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr12:88457843 G>A maps to NM_025114.3 Q2062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr12:88479848 T>C maps to NM_025114.3 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr12:88477725 T>C maps to NM_025114.3 Q1570Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:179989147 C>T maps to NM_014810.4 Q747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:180063621 G>A maps to NM_014810.4 K2794K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:180080148 G>A maps to NM_014810.4 E3069E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:179989420 A>C maps to NM_014810.4 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr1:180065276 T>A maps to NM_014810.4 Y3008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr1:179966253 C>G maps to NM_014810.4 S321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:180031410 G>T maps to NM_014810.4 L1773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:180034341 C>T maps to NM_014810.4 I1834I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:179966203 G>A maps to NM_014810.4 Q304Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr10:95276704 A>G maps to NM_018131.4 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr10:95287813 C>G maps to NM_018131.4 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr10:95276917 G>A maps to NM_018131.4 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr10:95276894 G>T maps to NM_018131.4 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr11:95546174 G>A maps to NM_014679.3 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr11:95532469 T>C maps to NM_014679.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:65299483 G>A maps to NM_015147.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr2:65299127 G>T maps to NM_015147.2 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr3:138227278 A>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:138256168 C>T maps to NM_024491.2 K162K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr3:138219387 G>A maps to NM_024491.2 Q464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr3:138289994 G>A maps to NM_024491.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:138289201 C>T maps to NM_024491.2 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr18:12674657 G>C maps to NM_024899.2 S573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr18:12702510 G>A maps to NM_024899.2 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr18:12673396 G>A maps to NM_024899.2 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr18:12686286 G>A maps to NM_024899.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:101451330 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:101483785 G>A maps to ENST00000327230 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:101476574 G>A maps to ENST00000327230 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr3:101484365 C>T maps to ENST00000327230 Q883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr3:101476878 G>T maps to ENST00000327230 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:101476527 C>T maps to ENST00000327230 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr3:101446300 G>A maps to ENST00000327230 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr3:101450782 C>A maps to ENST00000327230 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr1:111690492 G>T maps to NM_001007794.1 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:131190686 C>T maps to NM_016174.4 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr2:182413567 G>A maps to NM_001030311.2 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr16:55846892 A>T maps to NM_001025195.1 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:66975530 C>T maps to NM_003869.5 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr16:66977801 G>A maps to NM_003869.5 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr16:66974534 C>T maps to NM_003869.5 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:66969355 C>T maps to NM_003869.5 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr16:66997259 G>A maps to NM_024922.5 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr16:66998584 C>T maps to NM_024922.5 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr16:66998346 C>T maps to NM_024922.5 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr16:66997178 T>C maps to NM_024922.5 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr16:66997249 G>A maps to NM_024922.5 W84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr16:55883608 G>C maps to NM_001143685.1 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:55880714 C>T maps to NM_001143685.1 K487K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr16:67029589 C>T maps to ENST00000326686 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr18:580650 G>A maps to NM_004066.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr23:151996452 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:151996403 T>G did not map to a codon.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr23:151997113 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:151997169 C>A did not map to a codon.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr16:57007337 C>T maps to NM_000078.2 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:57016075 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:57009053 C>A maps to NM_000078.2 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:57007391 C>T maps to NM_000078.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr16:57012049 C>G maps to NM_000078.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr16:56995986 C>A maps to NM_000078.2 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:31919362 G>A maps to ENST00000437789 K1209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr6:31917908 C>A maps to ENST00000437789 A999A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr6:31918656 C>G maps to ENST00000437789 L1099L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr6:31914363 C>G maps to ENST00000437789 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:196646770 G>A maps to NM_000186.3 W198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr1:196709830 T>A maps to NM_000186.3 V955V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:196712594 G>A maps to NM_000186.3 V1049V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr1:196715007 G>A maps to NM_000186.3 P1124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:196659331 G>A maps to NM_000186.3 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:196695906 T>C maps to NM_000186.3 C691C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr1:196714953 A>G maps to NM_000186.3 T1106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:196715046 A>G maps to NM_000186.3 Q1137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:196797299 G>A maps to NM_002113.2 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:196928050 C>T maps to ENST00000367421 N218N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:196918657 A>G maps to ENST00000367421 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr1:196744060 T>C maps to NM_021023.5 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:196748484 C>T maps to NM_021023.5 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:196883725 G>T maps to NM_006684.2 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:196871590 A>G maps to NM_006684.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:196971610 G>T did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr1:196965185 C>A maps to ENST00000367414 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr1:196977800 T>C maps to ENST00000367414 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:196953097 T>C maps to ENST00000367414 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr4:110685754 T>A maps to ENST00000394635 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr11:65623176 C>T maps to NM_005507.2 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr11:65623617 C>T maps to NM_005507.2 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr11:65623611 C>T maps to NM_005507.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:65623629 C>G maps to NM_005507.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr11:65623476 G>A maps to NM_005507.2 C80C. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FD-A5C0-01A-11D-A289-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:202025317 G>A maps to NM_001127183.1 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr23:47485821 C>T did not map to a codon.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr7:117232104 G>A maps to NM_000492.3 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr7:117254745 C>A maps to NM_000492.3 S1149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr7:117180397 C>T maps to NM_000492.3 Q372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:87796143 C>A maps to NM_000735.2 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:49539428 G>A maps to ENST00000391869 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:49558232 G>A maps to ENST00000377280 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:151498240 G>T maps to NM_020770.2 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:151506504 C>A maps to NM_020770.2 R933R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:151491774 C>T maps to NM_020770.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:151492648 C>G maps to NM_020770.2 S294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:151496786 C>T maps to NM_020770.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr1:151497238 G>A maps to NM_020770.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:151491798 G>A maps to NM_020770.2 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr1:151502551 G>A maps to NM_020770.2 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:151497154 G>C maps to NM_020770.2 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr1:151504961 G>T maps to NM_020770.2 E886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr15:57730787 T>C maps to NM_032866.3 N197N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr15:57731768 G>A maps to NM_032866.3 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr2:27324699 G>A maps to ENST00000404694 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr15:41247689 T>C maps to NM_024111.3 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr15:41245948 C>T maps to NM_024111.3 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:48545625 C>T maps to NM_001267.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr17:48542793 C>T maps to NM_001267.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:4428818 C>G maps to NM_005483.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr19:4409113 C>T maps to NM_005483.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr21:37766928 C>T maps to NM_005441.2 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr21:37781086 A>C maps to NM_005441.2 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr21:37759966 C>G maps to NM_005441.2 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:50857601 C>T maps to NM_020549.4 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr10:50824127 G>A maps to NM_001142933.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr10:50872872 T>C maps to NM_020549.4 N676N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr10:50873007 C>T maps to NM_020549.4 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr10:50854653 C>G maps to NM_020549.4 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr10:50859928 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr10:75541895 G>A maps to NM_203298.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr10:75541949 G>A maps to NM_203298.2 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:132754903 G>C maps to ENST00000448878 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr7:132481276 C>A maps to ENST00000448878 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:126676357 C>T maps to ENST00000508789 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr8:57127186 A>G maps to NM_001011668.1 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr5:98228328 G>A maps to NM_001270.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:98232936 G>A maps to NM_001270.2 Q485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:98235319 G>A maps to NM_001270.2 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr5:98215418 G>C maps to NM_001270.2 S1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:98209359 C>A maps to NM_001270.2 E1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:98215332 G>A maps to NM_001270.2 R1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr5:98194719 C>G did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr5:98209410 G>A maps to NM_001270.2 R1153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr1:146758106 C>G maps to NM_004284.3 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:146763167 G>A maps to NM_004284.3 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr15:93534735 C>G maps to NM_001271.3 L1148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr15:93540503 C>G maps to NM_001271.3 V1252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr15:93558042 C>T maps to NM_001271.3 Q1604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr15:93563488 G>A maps to ENST00000309818 R1718R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr15:93563402 C>T maps to NM_001271.3 R1690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr15:93558042 C>T maps to NM_001271.3 Q1604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr15:93524071 G>A maps to NM_001271.3 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr15:93489417 C>G maps to NM_001271.3 S450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr15:93557923 A>T did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr17:7802504 C>T maps to NM_001005271.2 Y835Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:7797533 C>T maps to NM_001005271.2 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr17:7810215 T>C maps to NM_001005271.2 R1570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr17:7804635 C>G maps to NM_001005271.2 L1124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr17:7793897 G>T maps to NM_001005271.2 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr17:7812128 C>T maps to NM_001005271.2 F1851F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:6690249 C>G maps to ENST00000309577 V1651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr12:6700749 C>T did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr12:6682373 G>C maps to ENST00000309577 S1836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr12:6704528 C>A maps to ENST00000309577 E698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr12:6715470 A>C maps to ENST00000309577 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr12:6691314 C>T maps to ENST00000309577 L1529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:6709439 G>A maps to ENST00000309577 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr12:6691833 A>G maps to ENST00000309577 F1467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr1:6202307 C>T maps to NM_015557.2 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr1:6169927 G>A maps to NM_015557.2 L1835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:6189099 C>T maps to NM_015557.2 Q1139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:6206805 C>T maps to NM_015557.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:6173058 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:6195342 G>A maps to NM_015557.2 N939N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr1:6219572 C>T maps to NM_015557.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:6184140 C>A maps to NM_015557.2 G1522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:6173059 T>C did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:6208928 G>A maps to NM_015557.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:6184080 C>T maps to NM_015557.2 V1542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:6184140 C>A maps to NM_015557.2 G1522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:6208928 G>A maps to NM_015557.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:6181224 G>A maps to NM_015557.2 R1618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr1:6188916 G>C maps to NM_015557.2 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:6196892 G>C maps to NM_015557.2 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:6170531 G>C maps to NM_015557.2 L1768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:6196897 G>A maps to NM_015557.2 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:6186674 G>A maps to NM_015557.2 I1345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr20:40052252 C>T maps to NM_032221.3 W1478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr20:40053960 C>T maps to NM_032221.3 L1401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr20:40113103 G>A maps to NM_032221.3 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:40065974 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:40079710 C>T maps to NM_032221.3 G1186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr20:40049604 T>A maps to NM_032221.3 V1890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr20:40044140 G>C maps to NM_032221.3 L2208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr20:40116391 G>A maps to NM_032221.3 F638F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr20:40083313 C>T maps to NM_032221.3 Q1024Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:40084523 A>G maps to NM_032221.3 C975C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr20:40049238 T>A maps to NM_032221.3 T2012T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr20:40113085 G>A maps to NM_032221.3 F721F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr8:61655653 C>T maps to NM_017780.2 Q555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:61655514 T>C maps to NM_017780.2 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:61748693 C>T maps to NM_017780.2 Q1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:61693579 C>T maps to NM_017780.2 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:61693941 G>A maps to NM_017780.2 K683K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:61750315 C>T maps to NM_017780.2 F1425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr8:61654594 C>T maps to NM_017780.2 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr8:61654782 C>A maps to NM_017780.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr8:61748630 G>A did not map to a codon.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr8:61778137 G>A maps to NM_017780.2 P2880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr8:61761088 C>T maps to NM_017780.2 V1742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr8:61773575 T>G maps to NM_017780.2 L2574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr8:61765712 G>A maps to NM_017780.2 L2143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr8:61777945 G>A maps to NM_017780.2 L2816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr8:61765937 G>A maps to NM_017780.2 L2218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr8:61765125 G>A maps to NM_017780.2 V1988V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr8:61761112 A>G maps to NM_017780.2 Q1750Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr14:21870181 C>T maps to NM_001170629.1 Q1332Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr14:21894344 G>C maps to NM_001170629.1 S553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:21897299 C>T maps to NM_001170629.1 Q346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:21899342 G>A maps to NM_001170629.1 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr14:21884055 G>C maps to NM_001170629.1 S576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr14:21899133 C>T maps to NM_001170629.1 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr14:21861390 G>C maps to NM_001170629.1 L2114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr14:21861893 C>T maps to NM_001170629.1 E2020E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr14:21861378 C>T maps to NM_001170629.1 E2118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr16:53190093 A>G maps to ENST00000219084 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:53265677 G>A maps to ENST00000219084 R831R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr16:53281415 G>C did not map to a codon.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr16:53190975 C>T maps to ENST00000219084 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr16:53288442 C>T maps to ENST00000219084 R1319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr16:53326743 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:53190496 C>T maps to ENST00000219084 Q166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:53190558 C>G maps to ENST00000219084 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr3:53854559 G>T maps to NM_018397.4 S354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr3:53856586 C>T maps to NM_018397.4 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:53856610 G>C maps to NM_018397.4 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr22:29106035 G>A maps to NM_001005735.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr22:29092916 G>T maps to NM_001005735.1 S399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:16633880 C>T maps to NM_006387.5 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr19:16643431 C>G maps to NM_006387.5 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr19:16643506 C>G maps to NM_006387.5 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr19:16634036 C>T maps to NM_006387.5 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:133428209 G>A maps to NM_001161344.1 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:133433090 C>A maps to NM_001161344.1 E410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:133433091 C>A maps to NM_001161344.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr12:133420655 C>A maps to NM_001161344.1 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:133428240 C>T maps to NM_001161344.1 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr14:93393011 C>G maps to NM_001275.3 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr20:5904337 G>A maps to NM_001819.2 K516K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr20:5897482 C>T maps to NM_001819.2 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr20:5904367 C>T maps to NM_001819.2 Y526Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:5905693 G>A maps to NM_001819.2 *678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr20:5903650 G>A maps to NM_001819.2 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr1:111773469 C>T maps to NM_004000.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:111862082 G>A maps to NM_201653.2 Q390Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:111857894 C>T maps to NM_201653.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:870429 G>A maps to NM_001142676.1 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:884096 G>A maps to NM_001142676.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:902252 C>T maps to NM_001142676.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:203191374 G>C maps to NM_003465.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:203188876 G>T maps to NM_003465.2 S277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:67836401 G>T maps to NM_001277.2 S291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr22:51018829 A>G maps to NM_005198.4 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:51017893 G>T maps to NM_005198.4 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr22:51019954 G>A maps to NM_005198.4 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr3:440698 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:432753 T>C maps to NM_006614.2 F901F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr3:424355 T>A did not map to a codon.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr3:430986 G>A maps to NM_006614.2 W767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:431089 C>A maps to NM_006614.2 V801V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr23:85218980 T>A did not map to a codon.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr1:241797276 G>A maps to NM_001821.3 Q598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:241797667 C>T maps to NM_001821.3 K467K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr1:241797910 G>A maps to NM_001821.3 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr1:241798342 T>C maps to NM_001821.3 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:59063423 C>T maps to NM_014453.2 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr19:59065495 C>T maps to NM_014453.2 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:59063076 G>C maps to NM_014453.2 S203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr20:32436341 C>G maps to NM_176812.4 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr20:32399399 C>T maps to NM_176812.4 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr9:33270687 C>T maps to NM_016410.5 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:78971125 G>A maps to NM_024591.4 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:23112845 C>T maps to NM_152272.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr8:23115856 C>G maps to NM_152272.3 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr8:23112845 C>T maps to NM_152272.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr2:175809630 A>G maps to NM_001822.4 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr2:175666439 T>C maps to NM_001822.4 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:175664882 C>A maps to NM_001822.4 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr7:29440301 C>G maps to NM_004067.2 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr21:19632603 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:89956068 G>C maps to NM_012124.2 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr15:41549161 G>T maps to NM_007236.4 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:23767006 G>A maps to NM_022097.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr2:220406415 G>A maps to NM_024536.5 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr7:150934491 C>T maps to NM_019015.1 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr12:102110538 G>A maps to NM_020244.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:102091701 G>A maps to NM_020244.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr12:102107983 C>G maps to NM_020244.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:141525223 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr3:184100205 G>A maps to NM_003741.2 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:184099749 C>G maps to NM_003741.2 S214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:184099308 G>A maps to NM_003741.2 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr23:109943919 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr23:109964676 A>G did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:109919568 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:74419416 G>C maps to NM_015424.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr11:74429797 G>T maps to NM_015424.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr7:136700976 C>T maps to NM_001006628.1 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:136700169 C>G maps to NM_001006628.1 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr7:136700940 C>A maps to NM_001006628.1 C443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr7:136700394 G>A maps to NM_001006628.1 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr1:240072229 C>T maps to NM_000740.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:240071791 G>A maps to NM_000740.2 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:240072202 C>G maps to NM_000740.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:240072367 G>C maps to NM_000740.2 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:240072137 C>T maps to NM_000740.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr1:240072523 G>C maps to NM_000740.2 *591Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr11:46407252 G>A maps to NM_000741.2 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:34355560 C>T maps to NM_012125.3 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr2:175614814 C>T maps to NM_001039523.2 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr11:3687402 G>A maps to NM_020402.2 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr8:27327364 G>A maps to NM_000742.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr8:27321245 G>C maps to NM_000742.3 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr8:27324744 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:78894227 G>A maps to NM_000743.4 C252C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr15:78894560 G>C maps to NM_000743.4 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr20:61981889 G>C maps to NM_000744.5 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr20:61978167 G>A maps to NM_000744.5 F602F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr20:61982261 G>A maps to NM_000744.5 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr8:42611279 C>T maps to NM_004198.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr4:40351282 C>G maps to NM_017581.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr4:40351174 G>C maps to NM_017581.2 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr4:40339276 G>A maps to NM_017581.2 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr17:7350838 C>T maps to NM_000747.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:154543709 C>G maps to NM_000748.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:154544201 C>T maps to NM_000748.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr1:154548388 C>G maps to NM_000748.2 S497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:154548287 C>T maps to NM_000748.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:154544294 G>A maps to NM_000748.2 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr1:154544321 G>A maps to NM_000748.2 E341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr8:42586932 G>T maps to NM_000749.3 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr8:42587517 C>T maps to NM_000749.3 Y356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr15:78917492 G>A maps to NM_000750.3 Y493Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:233398642 C>G maps to NM_000751.1 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:233394688 C>A maps to NM_000751.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr2:233394808 C>T maps to NM_000751.1 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr2:233399895 G>A maps to NM_000751.1 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:4805237 C>T maps to NM_000080.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr2:233407217 G>T maps to NM_005199.4 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr2:233409213 C>G maps to NM_005199.4 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr11:45671792 G>C maps to NM_003654.4 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr11:45672446 G>C maps to NM_003654.4 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr11:45672161 G>A maps to NM_003654.4 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:45671594 G>C maps to NM_003654.4 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr11:45672395 G>A maps to NM_003654.4 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:101023083 G>A maps to NM_004854.3 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr12:105151418 G>A maps to NM_018413.5 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:105151253 C>G maps to NM_018413.5 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:2472654 G>C maps to NM_018641.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr7:2472762 C>T maps to NM_018641.3 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:126260808 C>T maps to NM_152889.1 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:126260859 C>T maps to NM_152889.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:40763861 C>G maps to NM_130468.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr10:125771921 G>A maps to NM_015892.3 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr10:125769697 G>A maps to NM_015892.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr10:125804237 G>A maps to NM_015892.3 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr3:142840194 C>T maps to NM_004267.3 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr10:73767199 C>T maps to NM_004273.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr10:73766944 G>C maps to NM_004273.4 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr16:71571353 G>A maps to NM_001166395.1 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr16:71571338 G>A maps to NM_001166395.1 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr16:75564159 G>A maps to NM_024533.3 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr16:75563649 G>A maps to NM_024533.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr16:75563931 C>T maps to NM_024533.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:75512841 G>A maps to NM_021615.4 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr16:75513366 G>C maps to NM_021615.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr16:75512817 G>A maps to NM_021615.4 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:46434112 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr23:46433886 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr23:46433798 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr23:46434157 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr19:34263196 G>A maps to NM_022467.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:101718243 C>T maps to NM_014918.4 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr15:101717592 T>G maps to NM_014918.4 *803Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr15:101718924 A>G maps to NM_014918.4 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:842557 C>T maps to ENST00000317063 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr16:844107 C>T maps to ENST00000455171 D647D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:845803 C>G maps to ENST00000317063 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr16:841360 G>A maps to ENST00000317063 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr16:846968 G>A maps to ENST00000317063 G1079G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr16:69154504 G>A maps to NM_001039690.3 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr16:69154381 G>T maps to NM_001039690.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:101959726 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr10:101967089 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr10:101953101 T>G maps to NM_001278.3 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:96932159 G>A maps to NM_004804.2 W24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:96936852 C>T maps to NM_004804.2 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr16:57470627 C>T maps to NM_020313.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr15:90774616 G>A maps to NM_006384.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr15:78403581 G>A maps to NM_006383.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr15:78403614 C>A maps to NM_006383.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr19:42796242 C>T maps to NM_015125.3 I964I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr19:42793046 T>C maps to NM_015125.3 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:42798382 C>A maps to NM_015125.3 S1418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:42797159 G>A maps to NM_015125.3 P1174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:42797417 G>A maps to NM_015125.3 K1260K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:42796293 G>C maps to NM_015125.3 L981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr19:42797367 C>A maps to NM_015125.3 R1244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:42796913 C>T maps to NM_015125.3 T1124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr18:12262871 G>C maps to ENST00000342845 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr18:12262896 C>A maps to ENST00000342845 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr16:11001757 G>A maps to NM_000246.3 A803A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr16:11000779 C>T maps to NM_000246.3 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr16:11000395 T>C maps to NM_000246.3 Y349Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr16:11000800 C>T maps to NM_000246.3 F484F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:11000923 C>G maps to NM_000246.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:11001259 C>T maps to NM_000246.3 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr15:65499183 G>A maps to NM_003613.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr15:65490151 G>A maps to NM_003613.3 V824V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr15:65491408 A>T maps to NM_003613.3 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr15:65489365 C>T maps to NM_003613.3 T1086T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:65494367 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr15:65490391 C>A maps to NM_003613.3 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr15:65491156 C>A maps to NM_003613.3 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr19:19656695 C>T maps to NM_153221.2 L1114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr19:19654823 C>T maps to NM_153221.2 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:19655507 C>T maps to NM_153221.2 N718N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr14:102814992 C>G maps to NM_001177611.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr19:1271011 C>G maps to ENST00000413636 S27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:1271018 C>T maps to ENST00000413636 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr19:1271438 C>T maps to NM_001280.2 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr16:69199281 T>C maps to NM_032830.2 D562D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr16:69189853 C>G maps to NM_032830.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:120159202 G>A maps to ENST00000392521 L1215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:120221777 C>T maps to ENST00000392521 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr12:120263154 C>T maps to ENST00000392521 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:120288004 G>T maps to ENST00000392521 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:120195198 C>T maps to ENST00000392521 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr12:120150420 G>A maps to ENST00000392521 S1553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr9:130928555 G>A maps to NM_012127.2 Q873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:53035695 A>G maps to NM_001098525.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr13:53030676 C>G maps to NM_001098525.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr13:53039468 C>T maps to NM_001098525.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:113498567 A>C maps to NM_152515.3 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr12:106632981 G>A maps to NM_006825.3 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr12:106633982 C>A maps to NM_006825.3 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr11:46806181 C>T maps to ENST00000415402 Q670Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:46812088 G>A maps to ENST00000415402 G565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr11:46810287 G>A maps to ENST00000415402 C637C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:46783564 G>A maps to ENST00000415402 F1402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr11:46786764 C>T maps to ENST00000415402 K1151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr11:46765596 C>T maps to ENST00000415402 E2032E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:46802035 C>T did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr11:46840015 C>T maps to ENST00000415402 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr14:103988659 G>A maps to NM_001823.3 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr16:66592157 C>T maps to NM_016951.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:45810761 G>A maps to NM_001824.3 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:45818822 G>C maps to NM_001824.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr19:45810803 G>T maps to NM_001824.3 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr15:43990903 C>T maps to ENST00000424065 D390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr15:43991211 G>A maps to ENST00000424065 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr5:80550234 C>T maps to NM_001825.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr1:154951210 C>T maps to NM_001826.2 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:122122824 G>A maps to NM_015282.2 L1308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr2:122216529 C>G maps to NM_015282.2 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr2:122363390 C>A maps to NM_015282.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr2:122187648 G>A maps to NM_015282.2 R673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr2:122154823 C>A maps to NM_015282.2 L1005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr2:122206564 G>C maps to NM_015282.2 S552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:33614642 G>A maps to ENST00000359576 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:33552168 G>A maps to ENST00000359576 Q1409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr19:40224975 G>A maps to NM_001828.4 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr1:86961220 C>G maps to NM_001285.3 S659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:86952366 C>T maps to NM_001285.3 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:86954770 C>A maps to NM_001285.3 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr1:86952414 C>T maps to NM_001285.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr1:86952297 A>G maps to NM_001285.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:86920976 C>T maps to NM_006536.5 R867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:86909546 C>T maps to NM_006536.5 N522N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:86913435 G>A maps to NM_006536.5 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr1:87040281 T>A maps to ENST00000263723 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:87041238 G>A maps to ENST00000263723 Q636Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:87040221 G>T did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:87045626 C>T maps to ENST00000263723 Q788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:87045737 G>T maps to ENST00000263723 E825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:109477396 G>C maps to NM_001048210.1 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr7:143039031 G>T maps to NM_000083.2 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr7:143018479 G>A maps to NM_000083.2 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr7:143016945 G>A maps to NM_000083.2 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr3:184075195 G>A maps to NM_004366.4 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:184075016 G>A maps to NM_004366.4 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr3:184075767 C>T maps to NM_004366.4 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr4:170608905 C>A maps to NM_173872.2 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr4:170634365 G>T maps to NM_173872.2 V762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr4:170618376 C>A maps to NM_173872.2 S352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr23:10176603 G>T did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr23:10188909 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr23:10188759 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr23:10155597 G>T did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:10163104 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr23:49837205 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:49837168 C>T did not map to a codon.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr23:49851523 G>T did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:49853458 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:49851018 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:49851279 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr23:49856836 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:49854785 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:11882770 G>A maps to ENST00000376496 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:11900228 C>T maps to NM_001286.2 L853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:11898674 G>A maps to ENST00000376496 T829T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:11894400 C>T maps to ENST00000376496 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr1:11882827 C>T maps to ENST00000376496 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:11893573 C>G maps to ENST00000376496 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr1:11883765 G>A maps to ENST00000376496 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr16:1510898 C>A maps to ENST00000382745 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:1510487 G>A maps to ENST00000382745 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:16358725 G>A maps to NM_004070.3 Q595Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr1:16353089 G>A maps to NM_004070.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr1:16375036 G>A maps to NM_000085.3 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:16372137 G>C maps to NM_000085.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:16375483 C>T maps to NM_001165945.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr1:16375546 G>A maps to NM_001165945.1 W27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:16382216 G>A maps to NM_000085.3 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr1:16373135 G>A maps to NM_000085.3 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr1:16374529 C>T maps to NM_000085.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr21:37833618 G>A maps to NM_001146077.1 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr21:37833621 G>C maps to NM_001146077.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr21:37833387 C>T maps to NM_001146077.1 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr21:37833717 G>A maps to NM_001146077.1 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:190105988 G>A maps to NM_006580.3 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:190120205 T>C maps to NM_006580.3 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr21:31538731 G>A maps to NM_012131.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr23:106171925 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:106171926 A>C did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr23:106171907 A>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:184241023 C>T maps to NM_001111319.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr8:8560285 C>T maps to NM_194284.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:113651014 C>G maps to NM_001101389.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:113651191 G>A maps to NM_001101389.1 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:113650685 C>T maps to NM_001101389.1 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:113650714 C>T maps to NM_001101389.1 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr7:73184118 G>A maps to NM_001306.3 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr7:73245563 C>T maps to NM_001305.3 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:73245998 G>A maps to NM_001305.3 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr22:19511529 G>A maps to NM_003277.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:3065462 G>T maps to NM_021195.4 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr16:3065983 C>G maps to NM_021195.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr17:7165242 G>A maps to NM_001185022.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:7165287 G>A maps to NM_001185022.1 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr16:3063905 C>G maps to NM_020982.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr16:3063893 C>T maps to NM_020982.3 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:98240495 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr17:6979313 G>A maps to NM_182906.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr17:6980294 G>A maps to NM_182906.2 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:6980294 G>A maps to NM_182906.2 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr19:51228558 C>T maps to NM_002975.2 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:10124257 C>T maps to ENST00000355690 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr14:38724399 G>A maps to NM_175060.1 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr16:11114143 C>T maps to ENST00000409790 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr16:11071189 C>T maps to ENST00000409790 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr16:11219834 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr16:11076790 G>T maps to ENST00000409790 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr16:11051689 G>A maps to ENST00000409790 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr16:11118743 G>T maps to ENST00000409790 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:14710592 C>T maps to ENST00000417570 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:74452025 T>A maps to NM_001011880.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr16:74452040 G>A maps to NM_001011880.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr16:74447571 G>A maps to NM_001011880.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr16:70208892 C>T maps to NM_173619.2 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:10149500 G>A maps to NM_016509.3 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:10149468 C>A maps to NM_016509.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr7:139229045 G>C maps to NM_001080511.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:7894073 C>A maps to NM_130441.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:7890170 C>A did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr12:8672820 G>C did not map to a codon.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr2:71043186 C>T maps to NM_173535.2 Q442Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:7794774 C>G maps to NM_198492.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr19:7833780 G>A maps to NM_014257.4 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr7:141643714 G>A maps to NM_013252.2 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr12:8612246 C>G maps to NM_001007033.1 S59*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-E5-A4U1-01A-11D-A31L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:10277985 G>A maps to NM_197947.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr12:9885671 G>A maps to NM_172004.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr4:141334193 C>A maps to NM_004362.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:31704044 G>A maps to NM_001288.4 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:154508586 G>A did not map to a codon.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr9:139889970 G>A maps to NM_004669.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:25167379 G>A maps to NM_013943.2 K238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr6:45922938 G>A maps to NM_001114086.1 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr6:45917027 G>T maps to NM_001114086.1 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr6:45917087 G>A maps to NM_001114086.1 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr21:36079651 C>T maps to ENST00000360731 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:122817643 C>G maps to ENST00000302528 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr12:122831942 C>T maps to ENST00000302528 Q495Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr12:122758619 C>G maps to ENST00000302528 L1352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:122825452 G>C maps to ENST00000302528 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr12:122845720 G>A maps to ENST00000302528 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr12:122818657 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:122845598 G>A maps to ENST00000302528 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr12:122838998 C>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr12:122763372 G>C maps to ENST00000302528 L1294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr12:122864954 G>A maps to ENST00000302528 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr7:73790515 G>A maps to NM_003388.4 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr7:73811472 G>C maps to NM_003388.4 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr19:36517130 G>C maps to NM_015526.2 S200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr19:36518042 G>A maps to NM_015526.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr2:29368222 C>T maps to ENST00000379543 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:29354253 T>C maps to ENST00000379543 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:29379281 G>T maps to ENST00000379543 E410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr2:29375568 C>G maps to ENST00000379543 S347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr2:29355040 G>C maps to ENST00000379543 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr2:201722760 A>G maps to NM_001162407.1 C242C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr1:155236634 G>A maps to ENST00000368361 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:155234439 G>A maps to ENST00000368361 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr15:74912355 C>T maps to NM_001130028.1 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr15:74912487 G>A maps to NM_001130028.1 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr15:74911639 C>T maps to NM_001130028.1 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr15:74921348 G>A maps to NM_001130028.1 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr5:178040552 G>A maps to NM_020666.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:92818692 G>A maps to NM_001025233.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:92814909 G>C maps to NM_001025232.1 S61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr12:92814854 C>G maps to NM_001025232.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr14:95669498 G>A maps to NM_024734.3 F729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr14:95688090 C>T maps to NM_024734.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr14:95679734 G>C maps to NM_024734.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr14:95688111 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr14:95657939 G>T maps to NM_024734.3 C990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr14:95670020 A>T maps to NM_024734.3 Y555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr13:77566268 G>A maps to NM_006493.2 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr15:68504195 G>A maps to NM_017882.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:68503653 G>A maps to NM_017882.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr15:68504081 G>A maps to NM_017882.2 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:1728459 G>A maps to NM_018941.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr8:1728490 C>T maps to NM_018941.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr4:56316354 G>A maps to NM_004898.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr4:56329884 C>A maps to NM_004898.2 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr4:56319882 G>C maps to NM_004898.2 S364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr11:57427172 G>C maps to NM_006831.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr11:72145269 G>A maps to NM_030813.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr11:72145374 C>G maps to NM_030813.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr11:72141360 G>A maps to NM_030813.3 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr11:72005415 C>A maps to NM_030813.3 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr11:72005476 C>T maps to NM_030813.3 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr11:72018298 C>A did not map to a codon.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr19:6366306 C>A maps to NM_006012.2 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr19:6361911 G>A maps to NM_006012.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr19:45476391 C>T maps to NM_001294.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:45477742 C>T maps to NM_001294.2 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr5:1321773 C>A maps to NM_030782.3 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr5:1322998 G>A maps to NM_030782.3 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr15:65447317 G>A maps to NM_006660.3 D471D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr3:150690270 C>T maps to NM_001195794.1 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr3:150690429 G>T maps to NM_001195794.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr3:150659507 G>A maps to NM_001195794.1 H98H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:150645818 C>G maps to NM_001195794.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr4:17528626 G>C maps to NM_001079827.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr10:129676574 C>T maps to NM_152311.3 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:36215405 C>A maps to NM_022111.3 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:36204800 A>G maps to NM_022111.3 L1122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr1:36228910 T>A maps to NM_022111.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:36202662 G>C maps to NM_022111.3 S1254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr1:36212456 G>A maps to NM_022111.3 Q922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr1:9793500 T>A maps to NM_001009566.1 S795S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:9815233 G>A maps to NM_001009566.1 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:9804540 G>C maps to NM_001009566.1 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:140185545 C>T maps to NM_022131.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr3:140140010 C>T maps to NM_022131.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr3:140123514 G>T maps to NM_022131.2 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr3:140285016 G>A maps to NM_022131.2 G930G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:140275362 C>T maps to NM_022131.2 F561F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr12:7293875 C>T maps to NM_014718.3 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr9:36209261 A>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr9:36191103 C>T maps to NM_007096.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr5:175823490 G>A maps to NM_007097.2 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr17:57754350 T>A maps to NM_004859.3 I866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr17:57737775 G>T maps to NM_004859.3 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr17:57758670 C>A maps to NM_004859.3 L1027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr22:19213750 G>C maps to NM_007098.3 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr22:19175537 C>G maps to NM_007098.3 V1463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr22:19188953 G>C maps to NM_007098.3 L1217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr22:19222103 C>T maps to NM_007098.3 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr22:19175582 C>A maps to NM_007098.3 V1448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr22:19263158 C>G maps to NM_007098.3 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:3554727 G>T maps to NM_015041.1 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:3554825 G>A maps to NM_015041.1 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr18:619336 G>C maps to NM_199167.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr18:624872 G>C maps to NM_199167.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr18:627095 G>T did not map to a codon.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr8:62212709 C>T maps to NM_173519.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr8:62412012 G>T did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr6:123319131 C>G maps to NM_001010852.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr6:123384817 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr6:123319060 C>T maps to NM_001010852.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr13:100425083 G>A maps to NM_206808.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr13:100543615 G>T maps to NM_206808.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr13:100543591 G>C maps to NM_206808.2 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr13:100511193 C>G maps to NM_206808.2 S110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr14:24975398 C>A maps to NM_001836.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr14:24975332 C>G maps to NM_001836.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr12:22213803 T>C maps to NM_018686.3 H244H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr12:22215237 C>T maps to NM_018686.3 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr12:22208136 T>A maps to NM_018686.3 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr16:81712221 C>T maps to NM_198390.2 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr16:81735359 C>A maps to NM_198390.2 R617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:108685926 G>A maps to NM_001142344.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr1:47840884 C>T maps to NM_016308.2 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr2:6990105 T>A did not map to a codon.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr2:7003613 G>A maps to NM_207315.2 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr16:66603972 G>A maps to NM_052999.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr16:66612825 C>T maps to NM_052999.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr16:66621937 A>G maps to NM_144673.2 K221K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:66651179 C>G maps to NM_178818.2 *235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr16:66670430 C>T maps to NM_178818.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr14:23846483 G>A maps to ENST00000339180 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr5:79031079 G>A maps to NM_153610.3 P2164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr5:79084913 C>T maps to NM_153610.3 L3892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr5:79026792 G>A maps to NM_153610.3 E735E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:79024843 G>T maps to NM_153610.3 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:79028134 G>T maps to NM_153610.3 E1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:79031289 T>G maps to NM_153610.3 A2234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:79031556 C>T maps to NM_153610.3 I2323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr5:79041274 G>A maps to NM_153610.3 L3655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr5:79054601 C>T maps to NM_153610.3 Q3713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr5:79025196 G>A maps to NM_153610.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr5:79057632 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr5:79025760 G>A maps to NM_153610.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr5:79058960 C>A maps to NM_153610.3 T3828T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr5:79027443 G>T maps to NM_153610.3 V952V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr5:79028227 C>T maps to NM_153610.3 Q1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr5:79033773 C>T maps to NM_153610.3 N3062N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr8:88218340 C>T maps to NM_173538.2 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr8:88297006 T>A maps to NM_173538.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr8:88218311 C>T maps to NM_173538.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr8:88249321 A>G maps to NM_173538.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr18:72228176 C>T maps to NM_032649.5 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr18:72179753 C>T maps to NM_018235.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr18:72168589 G>A maps to NM_018235.2 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:47938707 C>T maps to NM_001142564.1 Q670Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr4:47939151 G>C maps to NM_001142564.1 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr23:150911820 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:150912343 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr23:150909294 C>T did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:150912861 C>G did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr23:150912129 C>A did not map to a codon.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr23:150912943 G>C did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr23:150912795 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr23:150911829 C>A did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:150907009 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr2:98996643 G>A maps to NM_001298.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:99013468 C>T maps to NM_001298.2 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:98996643 G>A maps to NM_001298.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr2:98996706 G>A maps to NM_001298.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr2:99012571 C>T maps to NM_001298.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr16:57965710 C>A maps to NM_001297.4 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr16:57954289 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr16:58001045 C>A maps to NM_001297.4 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr16:57931374 G>T maps to NM_001297.4 I1056I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr8:87660076 G>A maps to NM_019098.4 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr8:87591075 C>T maps to NM_019098.4 Q648Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr11:66049794 G>T maps to NM_182553.1 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:224804935 C>T maps to NM_152495.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr1:224553635 C>G maps to NM_014184.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:26507028 C>T maps to ENST00000374253 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:26507067 C>T maps to ENST00000374253 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:26510260 G>A maps to ENST00000374253 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr23:21613155 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:21450808 T>C did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr23:21667010 G>C did not map to a codon.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr23:21550180 T>G did not map to a codon.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr23:21581436 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:21534626 G>C did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:21534644 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:21627228 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:21393071 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:154732194 C>T maps to NM_173515.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:154762423 A>C did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr6:154727694 G>A maps to NM_173515.2 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr6:154749282 C>G maps to NM_173515.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr19:11660486 C>A maps to NM_001299.4 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:11660188 C>A maps to NM_001299.4 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr19:1036476 C>G maps to NM_004368.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:1031128 C>A maps to NM_004368.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:95368701 G>A maps to NM_001839.3 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr10:101124710 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:104679814 C>T maps to NM_017649.3 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:104678578 G>A maps to NM_017649.3 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr10:104678596 C>T maps to NM_017649.3 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr10:104679088 G>C maps to NM_017649.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:104678700 C>G maps to NM_017649.3 S155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr10:104816705 C>T maps to NM_017649.3 F686F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr10:104679595 C>T maps to NM_017649.3 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr2:97483042 G>A maps to NM_017623.4 Q343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr2:97492618 G>A maps to NM_017623.4 K473K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr2:97483117 G>A maps to NM_017623.4 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr2:97427281 C>G maps to NM_020184.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:97475113 C>T maps to NM_020184.3 Q730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr2:97427797 C>T maps to NM_020184.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr2:97427383 C>T maps to NM_020184.3 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:97427797 C>T maps to NM_020184.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr2:97464823 C>G maps to NM_020184.3 S571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr4:6718463 G>A maps to NM_018366.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr16:58568056 C>T maps to NM_016284.3 L1963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr16:58571019 G>C maps to NM_016284.3 S1840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr16:58572153 G>A maps to NM_016284.3 R1718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr16:58576137 C>T maps to NM_016284.3 L1559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:58608567 G>A maps to NM_016284.3 Q642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:58573754 G>A maps to NM_016284.3 Q1637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:58621778 G>A maps to NM_016284.3 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:58621269 G>C maps to NM_016284.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:58621688 G>A maps to NM_016284.3 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr16:58620580 G>A maps to NM_016284.3 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr16:58621778 G>A maps to NM_016284.3 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:58565903 C>T maps to NM_016284.3 R2045R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr16:58614552 G>A maps to NM_016284.3 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:58568119 G>C maps to NM_016284.3 L1942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr16:58583727 G>C maps to NM_016284.3 V1139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr3:32745387 A>G maps to NM_015442.1 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr12:70672039 A>T maps to NM_014515.5 K12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr12:70732479 G>T maps to NM_014515.5 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:54656168 C>A maps to NM_014516.3 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:54649695 G>T maps to NM_014516.3 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr19:54656174 G>A maps to NM_014516.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:54656051 G>A maps to NM_014516.3 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr7:135099984 C>T maps to NM_001190850.1 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:78695756 G>A maps to ENST00000512485 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:17094803 T>G maps to NM_013354.5 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr5:154250349 C>T maps to NM_004779.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr7:99722456 A>G maps to NM_152755.1 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr6:88854585 C>A maps to NM_016083.4 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr6:88853766 C>T maps to NM_016083.4 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:24201128 C>A maps to NM_001841.2 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:246810439 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:246811272 G>A maps to NM_152609.2 E590E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:246810594 C>G maps to NM_152609.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr1:246811352 G>T maps to NM_001139459.1 *617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr19:40732341 C>G maps to NM_024877.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr19:40730478 G>A maps to NM_024877.3 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr19:40732353 C>A maps to NM_024877.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:58391556 G>A maps to NM_000614.3 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr11:58391532 C>T maps to NM_000614.3 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:17464509 G>A maps to NM_017738.2 E1140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr9:17466834 G>A maps to NM_017738.2 Q1267Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:17226273 G>T maps to NM_017738.2 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr9:17457538 G>A maps to NM_017738.2 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr12:41337896 C>T maps to NM_001843.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:41327359 A>T maps to NM_001843.2 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr12:41337509 A>G maps to NM_001843.2 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr12:41421764 A>G maps to NM_001843.2 G939G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr12:41421761 G>T maps to NM_001843.2 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:41337464 T>C maps to NM_001843.2 Y482Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr12:41386994 C>T maps to NM_001843.2 F679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:205042278 C>T maps to NM_005076.3 D976D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:205031668 C>A maps to NM_005076.3 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:205027350 C>T maps to NM_005076.3 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:205033501 C>A maps to NM_005076.3 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr1:205022372 C>G maps to NM_005076.3 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:205028798 C>T maps to NM_005076.3 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:74351883 C>T maps to NM_020872.1 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr3:74385745 A>C maps to NM_020872.1 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:74535679 T>C maps to NM_020872.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:74344387 C>G did not map to a codon.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr3:3081929 C>T maps to NM_175607.1 T791T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:2908607 T>C maps to NM_175607.1 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr3:3078872 C>T maps to NM_175607.1 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr3:2777957 T>C maps to NM_175607.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr3:3072564 C>T maps to NM_175607.1 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:2924919 T>C maps to NM_175607.1 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr11:100211903 A>G maps to NM_014361.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr11:100179089 G>T did not map to a codon.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr11:99944885 C>A maps to NM_014361.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr11:99715893 A>C maps to NM_014361.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr11:100061878 G>C maps to NM_014361.2 G534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr11:100064362 G>T maps to NM_014361.2 E618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr11:100226911 C>T maps to NM_014361.2 T1088T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr11:99715956 G>C maps to NM_014361.2 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr11:100170093 T>C maps to NM_014361.2 F862F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr3:1425079 G>T maps to NM_014461.2 V835V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr3:1424975 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:1262458 G>T maps to NM_014461.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr3:1337324 C>T maps to NM_014461.2 Y165Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr3:1320140 C>T maps to NM_014461.2 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr3:1415635 C>T maps to NM_014461.2 Y658Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:1363507 C>T maps to NM_014461.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr17:40837382 C>T maps to NM_003632.2 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr17:40839849 C>G maps to NM_003632.2 S386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr17:40838158 G>A maps to NM_003632.2 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr17:40841038 C>G maps to NM_003632.2 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr17:40843506 G>A maps to NM_003632.2 R774R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:40834846 C>A did not map to a codon.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr17:40837367 C>T maps to NM_003632.2 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr17:40840567 G>C maps to NM_003632.2 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr17:40847785 G>C maps to NM_003632.2 T1080T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr7:147600708 C>T maps to NM_014141.5 Y717Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr7:146536941 C>G maps to NM_014141.5 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr7:147600710 G>A maps to NM_014141.5 W718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr7:147092872 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:147869487 T>C maps to NM_014141.5 N976N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr7:147336398 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr7:147183134 T>C did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr7:146997348 C>T maps to NM_014141.5 Q489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr7:146805380 G>A maps to NM_014141.5 Q231Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:146471474 T>C did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:146536849 C>T maps to NM_014141.5 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:147815375 G>A maps to NM_014141.5 L850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr9:39178357 C>G did not map to a codon.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr9:39103885 G>A maps to NM_033655.3 F797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr16:76587219 G>T maps to NM_033401.3 A1160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr16:76486569 C>T maps to NM_033401.3 Q412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:76556044 A>G maps to NM_033401.3 E881E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr16:76495886 C>G maps to NM_033401.3 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr16:76572085 C>T maps to NM_033401.3 N1022N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr16:76513314 G>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr16:76532577 C>G maps to NM_033401.3 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr16:76350420 G>T did not map to a codon.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr2:125281919 C>A maps to NM_130773.2 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:125555700 G>A maps to NM_130773.2 T1006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr2:125261951 C>T maps to NM_130773.2 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:125504878 G>T maps to NM_130773.2 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:125521708 C>T maps to NM_130773.2 R839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr2:125671714 C>T maps to NM_130773.2 I1257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr2:125204408 G>A maps to NM_130773.2 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr2:125671723 G>C maps to NM_130773.2 R1260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr2:125261892 G>T maps to NM_130773.2 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr2:125175085 C>T maps to NM_130773.2 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:125521563 G>A maps to NM_130773.2 W790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr2:125262120 G>T maps to NM_130773.2 E438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr17:7838453 C>A maps to NM_001037144.4 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr17:7836432 C>T maps to NM_001037144.4 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:40716812 G>A maps to NM_001042532.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr7:51096212 C>T maps to ENST00000395542 Q942Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:51095843 C>T maps to ENST00000395542 Q1065Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:51092922 G>C maps to ENST00000395542 L1299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:51096732 G>T maps to ENST00000395542 S769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr7:51092856 T>C maps to ENST00000395542 Q1321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:51287547 G>A maps to ENST00000395542 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:51152987 G>T maps to ENST00000395542 S349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr7:51287508 C>A maps to ENST00000395542 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr7:51111332 G>A maps to ENST00000395542 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr7:51287508 C>T maps to ENST00000395542 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr2:165584635 C>T maps to ENST00000392717 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr2:165551328 G>C maps to ENST00000392717 S934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr9:140157644 G>T maps to NM_015456.3 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr9:140166653 C>T maps to NM_015456.3 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr9:140166659 C>G maps to NM_015456.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr9:140151343 G>A maps to NM_015456.3 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr9:140166600 C>T maps to NM_015456.3 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr14:31349662 C>T maps to NM_004086.2 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr14:31358870 G>C maps to NM_004086.2 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr17:71197987 C>T maps to NM_018714.2 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr17:71196743 C>G maps to NM_018714.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr17:71189297 C>T maps to NM_018714.2 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:230822833 C>T maps to NM_007357.2 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:230829036 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr13:46054310 G>A maps to NM_031431.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr13:46103944 G>A maps to NM_031431.2 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr13:46103989 G>A maps to NM_031431.2 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr13:46054406 A>G maps to NM_031431.2 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr16:70546312 C>G maps to NM_015386.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr16:70531254 C>T maps to NM_015386.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:70551627 C>T maps to NM_015386.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr16:70551591 G>A maps to NM_015386.2 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr7:106843965 G>A maps to NM_006348.3 Q860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr7:107167757 G>C maps to NM_006348.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr7:106871136 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr13:40239280 C>T maps to ENST00000255468 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr13:40293395 T>G maps to ENST00000255468 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:23400345 G>A maps to NM_153603.3 I736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr16:23415144 G>C maps to NM_153603.3 S558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr16:23436127 G>A maps to NM_153603.3 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr16:23453806 G>A maps to NM_153603.3 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr16:69369011 G>A maps to NM_032382.4 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:69368865 G>C maps to NM_032382.4 S324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:69370434 C>T maps to NM_032382.4 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:69370439 C>A maps to NM_032382.4 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:69373449 C>T maps to NM_032382.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr17:55027347 G>A maps to NM_004645.2 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:55038158 A>C maps to NM_004645.2 L74L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-E5-A4U1-01A-11D-A31L-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-FD-A3NA-01A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr6:116442381 C>T maps to ENST00000430695 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:103544383 T>C maps to NM_080629.2 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr1:103471859 G>A maps to NM_080629.2 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr1:103444469 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:103488405 G>A maps to NM_080629.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:103487274 T>C maps to NM_080629.2 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr1:103343586 A>G maps to NM_080629.2 C1815C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:103355069 C>A maps to NM_080629.2 E1481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:33146476 G>A maps to NM_080680.2 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:33135225 G>A maps to NM_080680.2 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:33154505 C>T maps to NM_080680.2 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr6:33144975 G>A maps to NM_080680.2 I666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr6:33141305 G>A maps to NM_080680.2 N885N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr6:33144777 G>A maps to NM_080680.2 D687D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr6:33156830 G>A maps to NM_080680.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr6:33139507 T>A maps to NM_080680.2 A1044A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:75797371 G>A maps to ENST00000322507 I3034I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr6:75811768 C>A did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr6:75887495 G>A maps to ENST00000322507 Q774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr6:75865541 G>C maps to ENST00000322507 L1093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr6:75898222 G>C maps to ENST00000322507 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr6:75851841 G>C maps to ENST00000322507 L1621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr6:75847184 G>A maps to ENST00000322507 Q1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr6:75812330 G>A maps to ENST00000322507 L2799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr6:75843687 C>G maps to ENST00000322507 L1850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:75798869 C>A maps to ENST00000322507 E2988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:75898183 G>A maps to ENST00000322507 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:75836143 C>T maps to ENST00000322507 W2128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr10:71716779 C>G maps to ENST00000356340 V711V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr10:71690163 C>T maps to ENST00000356340 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr10:71562458 C>T maps to ENST00000356340 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr8:121282334 T>C maps to NM_021110.1 D1045D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FM-01A-11D-A38G-08 chr8:121237451 C>T maps to NM_021110.1 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:121383404 C>T maps to NM_021110.1 Q1776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr8:121216071 C>T maps to NM_021110.1 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr8:121170471 G>A maps to NM_021110.1 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr8:121309826 G>C maps to NM_021110.1 L1438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr8:121220553 C>A maps to NM_021110.1 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr8:121312969 G>T did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:101825365 C>G maps to NM_001855.3 S1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:101767277 C>A maps to NM_001855.3 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:101748237 C>T maps to NM_001855.3 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr9:101817429 G>A maps to NM_001855.3 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr9:101797432 C>T maps to NM_001855.3 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr9:101830864 C>G maps to NM_001855.3 S1289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:32120447 C>T maps to NM_001856.3 V1434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr1:32146635 G>T maps to NM_001856.3 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:32162638 G>T maps to NM_001856.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:32140870 G>A maps to NM_001856.3 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr1:32149349 C>T did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:32157017 C>T maps to NM_001856.3 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr1:32146623 T>C maps to NM_001856.3 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr1:32120917 G>A maps to NM_001856.3 S1429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:32146635 G>A maps to NM_001856.3 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr10:105831837 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr10:105792001 G>C maps to NM_000494.3 V1495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr10:105817940 C>G maps to NM_000494.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr10:105793735 C>A maps to NM_000494.3 E1375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr10:105819883 G>A maps to NM_000494.3 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr21:46910214 C>T maps to ENST00000359759 P1077P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr21:46932165 G>T maps to ENST00000359759 E1707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr21:46911161 C>T maps to ENST00000359759 V1112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr21:46875521 G>C maps to ENST00000359759 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr21:46876058 C>G maps to ENST00000359759 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr21:46925816 C>T maps to ENST00000359759 L1466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:70909339 C>A maps to NM_001858.4 L1041L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr6:70861287 G>A did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr6:70589467 C>T maps to NM_001858.4 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:70890247 G>C maps to NM_001858.4 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr17:48273850 A>T maps to NM_000088.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr17:48263772 G>A maps to NM_000088.3 Q1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:48278868 G>A maps to NM_000088.3 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr7:94047864 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr7:94040247 C>T maps to NM_000089.3 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr7:94053673 G>A maps to NM_000089.3 Q864Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:94057006 C>T maps to NM_000089.3 Y1112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr7:94059611 A>G maps to NM_000089.3 P1336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr7:94057054 C>G maps to NM_000089.3 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr20:61944554 C>T maps to ENST00000326996 Y728Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr20:61936829 G>C maps to ENST00000326996 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr20:61936862 C>T maps to ENST00000326996 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr20:61941158 G>C maps to ENST00000326996 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr20:61943385 C>T maps to ENST00000326996 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FH-01A-11D-A38G-08 chr6:55929396 T>C maps to NM_030820.3 R717R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr6:56044500 G>C maps to NM_030820.3 S172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr6:56032951 T>C maps to NM_030820.3 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr8:139610970 T>C maps to NM_152888.1 P1452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr8:139697486 G>A maps to NM_152888.1 L977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr8:139833570 G>A maps to NM_152888.1 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:139629180 G>A maps to NM_152888.1 G1282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr8:139715554 A>G maps to NM_152888.1 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr8:139703090 G>A maps to NM_152888.1 P927P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr8:139691859 C>T maps to NM_152888.1 K1024K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr8:139707068 C>T maps to NM_152888.1 P882P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr8:139606404 C>T maps to NM_152888.1 A1490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr8:139609213 C>T did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr8:139729079 T>C maps to NM_152888.1 R796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr8:139601496 T>A maps to NM_152888.1 *1627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr8:139661982 G>A maps to NM_152888.1 L1124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:86591601 A>C maps to NM_152890.5 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:86203123 G>A maps to NM_152890.5 F1579F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr1:86249953 C>G maps to NM_152890.5 L1385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:86590557 C>G maps to NM_152890.5 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr4:109790267 G>A maps to ENST00000333642 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr4:109753533 A>G maps to ENST00000443653 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr4:109895712 G>A maps to ENST00000333642 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr4:109782093 G>A maps to ENST00000333642 Q411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr4:110222998 G>C maps to ENST00000333642 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr9:117044573 A>G maps to NM_032888.2 S1245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr9:116930500 G>T maps to NM_032888.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:117047050 C>T maps to NM_032888.2 G1327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr9:117002528 C>T maps to NM_032888.2 G919G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr9:116930563 G>A maps to NM_032888.2 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr9:117072973 G>A maps to NM_032888.2 *1861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr7:7546749 G>A maps to NM_001037763.2 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:7421177 C>T maps to NM_001037763.2 Q734Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr7:7514263 C>A maps to NM_001037763.2 G424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:48369178 G>A maps to NM_001844.4 I1269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr12:48375125 C>T maps to NM_001844.4 P821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:48393798 G>A maps to NM_001844.4 D65D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr12:48391688 C>A maps to NM_001844.4 G132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr2:189857620 T>A maps to NM_000090.3 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr2:189849537 C>G maps to NM_000090.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr2:189873942 G>A maps to NM_000090.3 K1273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr2:189876409 G>C maps to NM_000090.3 V1437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr2:189867022 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:189855741 C>T maps to NM_000090.3 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr13:110817221 C>T maps to NM_001845.4 P1379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr13:110828831 T>A maps to NM_001845.4 G999G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr13:110828801 T>G maps to NM_001845.4 P1009P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr13:110847442 G>A maps to NM_001845.4 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr13:110829253 C>T maps to NM_001845.4 Q949Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr13:110864215 G>A maps to NM_001845.4 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr13:111164535 T>G maps to NM_001846.2 *1713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr13:111164348 C>T maps to NM_001846.2 F1650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:228157989 A>T maps to NM_000091.4 G1098G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr2:228172495 G>A maps to NM_000091.4 W1441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:228174027 C>T maps to NM_000091.4 F1583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr2:228104884 C>T maps to NM_000091.4 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr5:74685494 C>T maps to NM_001130105.1 Q530Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr5:74806945 G>A maps to NM_001130105.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr5:74677902 C>T did not map to a codon.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr2:227896690 G>A maps to ENST00000396625 Q1263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr2:227953428 G>T maps to ENST00000396625 G521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:227898174 C>G maps to ENST00000396625 L1176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:227964339 G>C maps to ENST00000396625 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr2:227964338 T>A maps to ENST00000396625 K366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr2:227924257 G>T maps to ENST00000396625 S749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr2:227924262 G>A maps to ENST00000396625 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr23:107850089 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr23:107938637 C>A did not map to a codon.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr23:107930871 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr23:107840707 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr23:107939584 C>T did not map to a codon.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr23:107850105 G>A did not map to a codon.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr23:107938499 A>G did not map to a codon.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr23:107826119 C>T did not map to a codon.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr23:107824214 T>C did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:107939598 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr23:107439792 C>A did not map to a codon.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr23:107408601 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr23:107413847 C>T did not map to a codon.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr23:107434728 T>A did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr23:107433675 C>A did not map to a codon.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr23:107433640 T>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:107408247 G>T did not map to a codon.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr23:107403775 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr23:107423778 C>A did not map to a codon.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr23:107415702 C>G did not map to a codon.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr9:137717707 C>T maps to NM_000093.3 A1675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:137676851 C>T maps to NM_000093.3 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr9:137591827 C>T maps to NM_000093.3 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr9:137619131 C>G maps to NM_000093.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr9:137710578 G>A maps to NM_000093.3 P1436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr9:137655582 C>T maps to NM_000093.3 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:137711984 C>A maps to NM_000093.3 L1490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:137687130 C>G maps to NM_000093.3 P923P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr9:137658892 C>T maps to NM_000093.3 G727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr9:137582860 G>A maps to NM_000093.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:189950443 C>T did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:189904097 G>C maps to NM_000393.3 L1275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr2:189931118 T>C maps to NM_000393.3 E520E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr2:189904097 G>T maps to NM_000393.3 L1275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr19:10089566 C>T maps to NM_015719.3 P988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr19:10073542 G>A maps to NM_015719.3 S1601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr19:10080576 G>T maps to NM_015719.3 R1320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:10090717 G>A maps to NM_015719.3 L870L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr19:10071087 C>T maps to NM_015719.3 *1746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr19:10099814 T>C maps to NM_015719.3 G710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:10116260 G>A maps to NM_015719.3 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr19:10116236 G>A maps to NM_015719.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:10078592 G>C maps to NM_015719.3 S1464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr19:10100024 C>T maps to NM_015719.3 E688E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr21:47423836 C>T maps to NM_001848.2 G999G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr21:47419593 G>A maps to NM_001848.2 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr21:47420264 C>T maps to NM_001848.2 I599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr21:47423686 C>T maps to NM_001848.2 G949G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr21:47542435 C>T maps to NM_001849.3 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr21:47552033 C>T maps to NM_001849.3 R876R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr21:47531977 C>G maps to NM_001849.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:47538566 G>T maps to NM_001849.3 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr21:47549167 G>A maps to NM_058174.2 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr21:47531965 G>C maps to NM_001849.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr21:47532166 C>T maps to NM_001849.3 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr21:47544581 T>A maps to NM_001849.3 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:238283322 G>A maps to NM_004369.3 I1137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr2:238287357 T>C maps to NM_004369.3 P806P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:238285640 G>C maps to NM_004369.3 V948V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr2:238303320 A>C maps to NM_004369.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr2:238296564 G>A maps to NM_004369.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr2:238275411 G>A maps to NM_004369.3 S1806S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:238277470 G>C maps to NM_004369.3 V1545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr2:238285670 A>G maps to NM_004369.3 D938D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr2:238277739 G>A maps to NM_004369.3 R1456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr2:238243311 C>T maps to NM_004369.3 L3062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr2:238283454 G>A maps to NM_004369.3 N1093N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr3:130312093 C>T maps to NM_001102608.1 Q1490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr3:130282311 G>A maps to NM_001102608.1 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr3:130287161 G>C maps to NM_001102608.1 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:130287182 C>T maps to NM_001102608.1 F712F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr3:130282180 C>T maps to NM_001102608.1 Q112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr3:130381084 C>G maps to NM_001102608.1 G2145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr3:130380586 T>A maps to NM_001102608.1 A1979A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr3:130293316 G>A maps to NM_001102608.1 K1165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:130318626 C>A maps to NM_001102608.1 P1542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr3:130380796 C>T maps to NM_001102608.1 H2049H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr3:130305458 C>A maps to NM_001102608.1 L1360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr3:130289660 G>A did not map to a codon.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr3:48605195 C>A maps to NM_000094.3 G2644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:48626327 G>C maps to NM_000094.3 Y805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:48613975 G>A maps to NM_000094.3 V1905V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:48630667 C>T maps to NM_000094.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr3:48623283 C>T maps to NM_000094.3 Q1255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr3:48622543 G>A maps to NM_000094.3 F1300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr3:48611122 C>T maps to NM_000094.3 P2191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr3:48616695 G>T maps to NM_000094.3 P1774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr3:48612911 G>A maps to NM_000094.3 Q2014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:48623587 G>A maps to NM_000094.3 F1214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr3:99513683 C>T maps to ENST00000429802 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr3:99514903 C>A maps to ENST00000429802 S721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr3:99513617 T>C maps to ENST00000429802 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr1:36563217 C>T maps to NM_005202.2 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47S-01A-11D-A23U-08 chr6:71004165 G>A maps to NM_001851.4 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:70944595 C>T maps to NM_001851.4 R720R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:70964890 T>G maps to NM_001851.4 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr6:71010033 C>T maps to NM_001851.4 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:71010048 G>C maps to NM_001851.4 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr6:70981387 G>A maps to NM_001851.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr1:40779875 C>T did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr20:61467684 G>C maps to NM_001853.3 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr20:61458603 C>T maps to NM_001853.3 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr2:3691368 G>A maps to ENST00000418971 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr18:346721 G>A maps to NM_130386.2 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr18:333005 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr18:346708 G>A maps to NM_130386.2 Q305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr18:346397 C>G maps to NM_130386.2 S408S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-E7-A4IJ-01A-31D-A26M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:15563060 C>A maps to NM_005677.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr15:75631431 G>A maps to NM_017828.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr20:31292655 C>G maps to NM_053041.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr20:31292697 C>T maps to NM_053041.2 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:36302291 G>A maps to NM_014186.3 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:18896557 G>A maps to NM_000095.2 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:18895846 G>T maps to NM_000095.2 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr19:18897059 G>A maps to NM_000095.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr19:18896512 C>T maps to NM_000095.2 Q546Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr22:19951737 G>A maps to NM_001135162.1 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr22:19951111 C>T maps to NM_001135162.1 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr22:19951776 C>G maps to NM_001135162.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr22:19951737 G>A maps to NM_001135162.1 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr10:76993968 C>T maps to NM_144589.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr10:76993950 C>T maps to NM_144589.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:160262954 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr1:160261930 G>A maps to NM_001098398.1 L1015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:160264383 C>G did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:160280026 G>A maps to NM_001098398.1 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr1:160261130 G>T maps to NM_001098398.1 A1147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:160283853 G>C maps to NM_001098398.1 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:160268718 C>T maps to NM_001098398.1 K640K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:160268935 C>A maps to NM_001098398.1 E605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:160275263 G>A maps to NM_001098398.1 I551I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr11:14515868 G>A maps to NM_001144061.1 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:14502616 T>C maps to NM_001144061.1 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr11:14512188 C>T maps to NM_001144061.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr3:139081295 G>A maps to NM_004766.2 Q650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:139102139 C>T maps to NM_004766.2 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:139092110 C>T maps to NM_004766.2 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr3:139085499 G>A maps to NM_004766.2 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr3:128982805 C>G maps to NM_016128.3 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:128991686 C>G maps to NM_016128.3 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr3:128971203 G>A maps to NM_016128.3 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr3:128979194 C>T maps to NM_016128.3 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr3:128973916 C>T maps to NM_016128.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr3:128971194 C>T maps to NM_016128.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr15:49423005 G>A maps to NM_001143887.1 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr4:83996451 C>T maps to ENST00000503682 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr4:83996468 G>A maps to ENST00000503682 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr4:83978133 C>T maps to ENST00000503682 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr8:67974119 C>A maps to NM_006837.2 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:99686982 C>G maps to NM_006833.4 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:54741571 A>C maps to NM_016057.1 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:56663998 C>G maps to NM_144576.3 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:56664099 G>C maps to NM_144576.3 *248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr2:198324751 C>T maps to NM_025147.3 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr4:84193255 C>T maps to NM_015697.7 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:99823965 G>A maps to NM_017421.3 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr6:99819439 A>G maps to NM_017421.3 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr6:99817476 C>A maps to NM_017421.3 *370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr6:99828201 T>C maps to NM_017421.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:131087435 C>T maps to NM_016035.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:131095146 G>A maps to NM_016035.3 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:120942705 G>C maps to NM_032314.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr12:120960043 G>A maps to NM_032314.3 Q109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:120954475 C>T maps to NM_032314.3 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMJ-01A-11D-A42E-08 chr12:120954397 C>T maps to NM_032314.3 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMJ-01A-11D-A42E-08 chr12:120954535 C>T maps to NM_032314.3 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:74425723 G>A maps to NM_182476.1 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr14:74424974 T>C maps to NM_182476.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr16:57490840 A>G did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr4:47746493 G>A maps to NM_006587.2 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr4:47809061 G>T maps to NM_006587.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr4:47645188 G>T maps to NM_006587.2 S681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr4:47676440 G>A maps to NM_006587.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr16:30199707 C>A maps to NM_007074.3 Y364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr16:30198258 C>T maps to NM_007074.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr16:30199131 C>A maps to NM_007074.3 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:30199779 C>G maps to NM_007074.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr11:67209532 C>T maps to NM_020441.2 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr11:67205879 C>T maps to NM_020441.2 E479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr11:67208696 C>A maps to NM_020441.2 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr9:100888881 C>G maps to NM_052820.3 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr9:100892139 G>A maps to NM_052820.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr9:100890921 G>A maps to NM_052820.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr15:68987594 G>A maps to NM_006091.3 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr15:69011860 A>G maps to NM_006091.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr15:69003960 C>T maps to NM_006091.3 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:27945891 C>T maps to ENST00000345068 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:27943317 G>A maps to ENST00000345068 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:27943796 G>A maps to ENST00000345068 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:4412078 G>A maps to NM_024535.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr16:4411440 C>T maps to NM_024535.3 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:4408478 G>A maps to NM_024535.3 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:14095374 G>A maps to NM_001303.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr17:53045650 G>C maps to NM_004375.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr17:53045776 C>G maps to NM_004375.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr17:53045688 G>A maps to NM_004375.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr10:101489362 G>T maps to NM_078470.4 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr10:101487207 C>A maps to NM_078470.4 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr14:70826256 G>C maps to NM_016468.5 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr4:73923840 G>C maps to NM_173827.2 S331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr16:85814058 C>A maps to NM_006067.4 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr16:85832889 C>T maps to NM_006067.4 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:98263593 G>A maps to NM_001862.2 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:120875951 C>A maps to NM_004373.2 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr6:75953505 C>T maps to NM_001865.3 W14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr6:75953495 C>A maps to NM_001865.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr23:77160726 G>A did not map to a codon.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr4:46737170 G>A maps to NM_130902.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr3:148925366 G>C maps to NM_000096.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr3:148917643 G>A maps to NM_000096.3 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr3:148939522 C>T maps to NM_000096.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr3:148925198 C>T maps to NM_000096.3 Q329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr3:148896412 G>A maps to NM_000096.3 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr16:19547560 C>G maps to NM_014711.4 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr16:19556149 C>G maps to NM_014711.4 S839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr16:19543790 T>C maps to NM_014711.4 D65D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr16:19559275 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr7:130023556 C>T maps to NM_001868.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr7:130025131 C>G maps to NM_001868.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr7:129908840 A>G maps to NM_001869.2 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:129916529 C>T maps to NM_001869.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:129910553 G>T maps to NM_001869.2 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr7:129929453 C>G maps to NM_001869.2 S376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr3:148614343 C>T maps to NM_001870.2 D368D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr3:148614376 C>T maps to NM_001870.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr7:129950684 G>A maps to NM_016352.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr7:129945684 G>A maps to NM_016352.3 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr7:129938636 G>A maps to NM_016352.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr7:129933088 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr7:130008338 T>C maps to NM_080385.4 Y404Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:68536431 C>T maps to NM_020361.4 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr8:68658295 C>T maps to NM_020361.4 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr8:68334768 G>T maps to NM_020361.4 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr19:17081738 C>T maps to ENST00000443236 G782G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr19:17081753 G>A maps to ENST00000443236 F777F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr19:17057908 G>A maps to ENST00000443236 S936S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr19:17104255 G>T maps to ENST00000443236 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr19:17039044 C>G did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr19:17038867 G>A maps to ENST00000443236 V1164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:17132939 G>A maps to ENST00000443236 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr19:17100521 G>A maps to ENST00000443236 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr19:17039805 G>C maps to ENST00000443236 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr19:17108127 G>A maps to ENST00000443236 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr3:148545857 G>A maps to NM_001871.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr3:148575266 G>A maps to NM_001871.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr3:148563269 G>T maps to NM_001871.2 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:148575326 C>T maps to NM_001871.2 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr13:46638787 C>T maps to NM_001872.3 W264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr13:46656652 G>A maps to NM_001872.3 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr13:46638813 C>T maps to NM_001872.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr17:28758883 A>T maps to NM_001304.4 A704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr17:28754485 C>T maps to NM_001304.4 Q643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:28770947 C>T maps to NM_001304.4 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:28749992 G>T maps to NM_001304.4 E537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr17:28789484 C>G maps to NM_001304.4 S1305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:28749807 C>G maps to NM_001304.4 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr17:28706543 C>G maps to NM_001304.4 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr17:28776729 C>T maps to NM_001304.4 L1011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr17:28706483 C>T maps to NM_001304.4 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr4:166414358 C>T maps to NM_001873.2 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr4:166388837 A>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:83222280 A>C maps to ENST00000261723 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr10:93841144 G>A maps to NM_014912.4 Q601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr10:93870927 C>A maps to NM_014912.4 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr5:173317474 C>T maps to NM_030627.2 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr4:780371 C>A maps to NM_006651.3 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr15:75122673 T>C maps to NM_001030005.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr12:69326599 G>A maps to NM_001874.4 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr10:101823404 G>A maps to NM_001308.2 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr20:34214644 C>G maps to NM_003915.5 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr20:34220268 C>A maps to NM_003915.5 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:34219935 T>A maps to NM_003915.5 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr20:34219188 C>G did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr20:34218893 C>T maps to NM_003915.5 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr20:34219049 G>A maps to NM_003915.5 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr20:34219207 G>A maps to NM_003915.5 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr8:87568346 G>A maps to NM_003909.3 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr8:87540814 C>T maps to NM_003909.3 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr8:87563279 G>A maps to NM_003909.3 K340K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr3:131293968 G>A maps to ENST00000502818 H309H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr3:131261496 C>T maps to ENST00000502818 Q499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:131388548 T>G maps to ENST00000502818 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:36724063 C>T maps to NM_020939.1 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr14:24546430 C>T maps to NM_006032.2 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr14:24546220 G>A maps to NM_006032.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr12:39047684 C>T maps to NM_153634.2 *565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FH-01A-11D-A38G-08 chr3:9757191 A>G maps to ENST00000383832 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:9759782 C>T maps to ENST00000383832 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr3:98311802 C>T maps to NM_000097.5 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr16:12758793 C>G maps to NM_018340.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr16:12758793 C>T maps to NM_018340.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:211513261 G>A maps to NM_001122633.1 L1140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr2:211525294 G>A maps to NM_001122633.1 K1287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr2:211464285 G>C did not map to a codon.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr2:211454828 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:145625826 C>T maps to NM_013291.2 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr8:145624216 G>A maps to NM_013291.2 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr8:145625557 A>G did not map to a codon.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr8:145624758 C>T maps to NM_013291.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr8:145622830 G>C maps to NM_013291.2 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:92608527 C>T maps to NM_017437.1 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr14:92600429 C>A maps to NM_017437.1 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr14:92601739 C>T maps to NM_017437.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr2:9576353 G>A maps to NM_016207.2 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr2:9572669 C>T maps to NM_016207.2 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr2:9570976 T>C maps to NM_016207.2 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:1248251 G>A maps to NM_017871.4 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr7:99042454 C>T maps to NM_006693.2 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:99048376 C>T maps to NM_006693.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr12:69652415 T>G maps to ENST00000266679 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr12:69656251 G>A maps to ENST00000266679 E560E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr11:61196737 G>A maps to NM_024811.3 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr11:61183839 C>T maps to NM_024811.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr11:61196667 C>A maps to NM_024811.3 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr11:61188951 G>A maps to NM_024811.3 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr11:68525171 C>G maps to NM_001876.3 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr11:68560834 G>A maps to NM_001876.3 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr11:68527752 C>A maps to NM_001876.3 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr22:51010512 C>T maps to NM_152245.2 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr22:51011388 C>A maps to NM_152245.2 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr7:29105665 A>G maps to NM_031311.3 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr7:29132261 G>A maps to NM_031311.3 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:88008542 A>C did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:88008580 G>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr23:88009142 A>C did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr20:2778919 G>C maps to NM_019609.4 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr10:125528080 G>A maps to NM_198148.2 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr10:125521535 G>A maps to NM_198148.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr4:8602923 C>T maps to NM_001014447.2 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr4:8616128 C>T maps to NM_001014447.2 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:207789923 C>A maps to NM_000651.4 I2222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:207753874 C>T maps to NM_000651.4 F1711F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr1:207791494 C>T maps to NM_000651.4 I2323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:207758063 C>A maps to NM_000651.4 P1791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr1:207818617 C>A maps to NM_175710.1 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr1:207890998 C>T maps to NM_175710.1 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr1:207640066 C>T maps to NM_001006658.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:207651345 G>T maps to NM_001006658.2 E1007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:207646466 C>T maps to NM_001006658.2 Q641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr1:207644372 C>G maps to NM_001006658.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr1:207642004 G>A maps to NM_001006658.2 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr1:207643299 C>T maps to NM_001006658.2 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:207644083 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:78635839 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr16:1719032 G>A maps to NM_020825.3 L1122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr16:1706029 G>T maps to NM_020825.3 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr16:1691167 G>C maps to NM_020825.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr9:131866464 A>G did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr1:197396998 C>T maps to NM_201253.2 F848F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr1:197390571 A>G maps to NM_201253.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:197411331 G>T maps to NM_201253.2 P1305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr1:197390533 C>T maps to NM_201253.2 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:197298071 C>T maps to NM_201253.2 N197N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr1:197313414 A>G maps to NM_201253.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:197398671 G>T maps to NM_201253.2 E924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr1:197390556 G>C maps to NM_201253.2 V533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr9:126125324 C>T maps to NM_173689.5 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr9:126133463 C>T maps to NM_173689.5 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr9:126133736 C>T maps to NM_173689.5 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:6466562 G>A maps to NM_174881.2 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7N-01A-11D-A391-08 chr9:35735305 C>G maps to NM_006368.4 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:35736617 C>G maps to NM_006368.4 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:35732997 G>A maps to NM_006368.4 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr9:35735134 G>C maps to NM_006368.4 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr11:46329487 C>T maps to ENST00000288400 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr11:46333970 C>A maps to ENST00000288400 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr7:137570247 C>T maps to NM_194071.2 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr19:4170196 G>A maps to NM_032607.1 K294K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:4159760 G>A maps to NM_032607.1 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr19:4157026 C>T maps to NM_032607.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:153946366 G>A maps to NM_130898.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:153941063 G>C maps to NM_130898.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr7:28858776 C>T maps to NM_182898.2 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:28763906 T>A maps to NM_182898.2 C220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr7:28843820 G>A maps to NM_182898.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:28858827 G>T maps to NM_182898.2 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:28848985 G>A maps to NM_182898.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr7:28725798 C>A maps to NM_001011666.1 S11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr7:28610059 C>T maps to NM_182898.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr16:3786649 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr16:3808022 G>A maps to NM_004380.2 P1132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr16:3817737 G>T maps to NM_004380.2 S1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr16:3817749 G>C maps to NM_004380.2 S1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:3820791 G>A maps to NM_004380.2 Q887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:3820951 G>C maps to NM_004380.2 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr16:3820935 G>A maps to NM_004380.2 Q839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:3807964 G>A maps to NM_004380.2 Q1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr16:3786147 A>C maps to NM_004380.2 Y1539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:3789684 G>A maps to NM_004380.2 R1392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:3824684 G>T maps to NM_004380.2 S723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr16:3900804 C>T maps to NM_004380.2 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr16:3820719 G>A maps to NM_004380.2 Q911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr16:3799626 C>T did not map to a codon.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr16:3830775 C>A maps to NM_004380.2 E594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:3778369 C>T maps to NM_004380.2 A2226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:3828042 C>T maps to NM_004380.2 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr16:3779714 G>T maps to NM_004380.2 S1778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr16:3786705 C>T maps to NM_004380.2 W1502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:3777745 C>T maps to NM_004380.2 T2434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:3823903 G>A maps to NM_004380.2 Q771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr16:3779152 C>T maps to NM_004380.2 E1965E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr16:3820784 G>C maps to NM_004380.2 S889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr16:3831262 G>A maps to NM_004380.2 Q540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr16:3841996 T>A maps to NM_004380.2 K439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr16:3808852 A>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr16:3795300 G>A maps to NM_004380.2 H1297H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr16:3831262 G>A maps to NM_004380.2 Q540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr2:101971828 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr2:101971818 G>A maps to NM_153836.3 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:101967408 G>A maps to NM_153836.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:9979320 G>A maps to NM_001077415.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr3:9976245 C>T maps to NM_001077415.2 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr3:9986217 A>T maps to NM_001077415.2 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr22:50318083 G>A maps to NM_001135101.1 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr10:35477262 C>G maps to ENST00000429130 S215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:35500211 G>A maps to ENST00000374721 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr8:67089286 G>A maps to NM_000756.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:67089334 G>A maps to NM_000756.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:43912039 G>A maps to NM_001145146.1 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:43910816 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr7:30721546 G>C maps to ENST00000348438 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr7:30704744 G>A maps to ENST00000348438 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr7:30704789 G>A maps to ENST00000348438 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:36583614 C>T maps to NM_016441.2 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr14:105954726 T>C did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr14:105954548 G>A maps to NM_001311.4 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr4:1388589 C>G maps to NM_175918.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr6:49666125 G>A maps to ENST00000211238 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr6:49698955 C>T maps to NM_001190986.1 W200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr8:75927100 C>A maps to NM_031461.5 C227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr8:75926322 C>T maps to NM_031461.5 C204C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:84883008 C>T maps to NM_031476.3 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:84872124 C>A maps to NM_031476.3 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr16:84879411 G>A maps to NM_031476.3 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr17:1359264 G>A maps to NM_016823.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:21272302 G>A maps to NM_005207.3 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:18705143 C>T maps to NM_004750.4 K375K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:18705188 C>G maps to NM_004750.4 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr23:1327783 G>A did not map to a codon.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr23:1325409 C>A did not map to a codon.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr17:29119480 G>A maps to NM_015986.3 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr20:6015165 C>T maps to NM_019095.4 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr4:5827317 G>C maps to NM_001014809.1 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:5827254 G>A maps to NM_001014809.1 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr4:5838494 C>T maps to NM_001014809.1 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr4:5837698 G>A maps to NM_001014809.1 D522D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr4:5830230 G>C maps to NM_001014809.1 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr4:5844872 G>A maps to NM_001014809.1 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:20020279 G>A maps to NM_016652.4 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr20:20033190 C>T maps to NM_016652.4 K93K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr20:20029078 G>A maps to NM_016652.4 Y282Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr20:20018014 G>C maps to NM_016652.4 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr20:20033196 G>A maps to NM_016652.4 C91C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr1:152382699 A>G maps to NM_016190.2 H286H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr1:152383080 A>T maps to NM_016190.2 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr1:152384702 G>A maps to NM_016190.2 Q3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:17292233 C>T maps to NM_014675.3 L1474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr1:17257072 G>A maps to NM_014675.3 W278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:87006663 G>A did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr7:86998690 G>C did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr7:87022133 C>G maps to NM_001143935.1 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr7:86998749 C>G maps to NM_001143935.1 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr7:86998690 G>C did not map to a codon.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr1:159683743 G>C maps to NM_000567.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:159683509 G>A maps to NM_000567.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:159683377 G>A maps to NM_000567.2 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:99655722 G>A maps to NM_018058.4 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr10:99770956 G>C maps to NM_018058.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr10:99661303 G>A maps to NM_018058.4 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr11:122742104 T>C maps to NM_019604.2 *394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr11:122738807 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr3:33156036 C>T maps to NM_006371.4 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:18864348 C>A maps to NM_001098482.1 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:18885711 C>T maps to NM_001098482.1 H492H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr19:18870883 G>T maps to NM_001098482.1 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:18860677 G>A maps to NM_001098482.1 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr1:153930898 C>T maps to NM_181715.2 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:153920994 G>A maps to NM_181715.2 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:153921066 A>G maps to NM_181715.2 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr1:153930886 C>T maps to NM_181715.2 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:153923846 G>T maps to NM_181715.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr1:153930886 C>T maps to NM_181715.2 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr1:153930898 C>T maps to NM_181715.2 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr15:91083356 G>A maps to NM_022769.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr15:91136981 C>T maps to NM_022769.3 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr15:91172565 C>T maps to NM_022769.3 N356N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr19:48343212 C>T maps to NM_000554.4 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr12:107393523 G>T maps to NM_004075.3 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:45891635 C>T maps to NM_021117.3 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:44590649 C>T maps to NM_000394.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr11:111781083 C>G maps to NM_001885.1 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:27579108 C>T maps to NM_005208.4 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr22:27024277 C>A maps to NM_001886.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:27003913 C>T maps to NM_001887.3 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr22:27008145 G>T maps to NM_001887.3 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr22:26997880 G>A maps to NM_001887.3 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr22:25617443 C>T maps to NM_000496.2 N16N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr22:25623910 C>T maps to NM_000496.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr22:25599846 C>G maps to NM_004076.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:97618082 C>T maps to ENST00000182096 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr3:97634462 C>T maps to ENST00000182096 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr2:208986529 C>T maps to NM_006891.3 W131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:186256613 G>C maps to NM_017541.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr13:21006312 C>T maps to NM_015974.2 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr13:21013866 C>T maps to NM_015974.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr13:21063598 C>T maps to NM_015974.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:21272617 C>T maps to NM_001888.3 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr16:21272572 A>T did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:75188927 A>T maps to NM_001889.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr21:34994368 C>T maps to ENST00000416217 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr12:56667505 C>T maps to NM_004077.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr12:56668662 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:53565115 C>G maps to NM_015989.4 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr23:151908926 A>T did not map to a codon.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr23:151909154 A>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr23:151909196 G>T did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr22:41968113 C>T maps to NM_014460.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:115262242 G>A maps to NM_001130523.1 Q740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:115268893 C>T maps to NM_001130523.1 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr20:47707528 C>T maps to NM_001316.2 Q779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr20:47707557 G>A maps to NM_001316.2 K788K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr20:47707560 T>G did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:47704591 C>T maps to NM_001316.2 Y590Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:47706099 G>A maps to NM_001316.2 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:47683034 C>A maps to NM_001316.2 S155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr20:47682760 C>T maps to NM_001316.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr20:47700666 C>G maps to NM_001316.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr20:47707503 C>A maps to NM_001316.2 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:110466436 G>A maps to NM_000757.4 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:110467772 C>T maps to NM_000757.4 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr1:110466685 T>C maps to NM_000757.4 H481H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:149440455 G>A maps to NM_005211.3 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr23:1409270 C>G did not map to a codon.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr23:1409370 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:1419438 G>C did not map to a codon.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr23:1407681 C>G did not map to a codon.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr23:1407522 T>C did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:1401660 C>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:1422828 G>T did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:1404675 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr23:1409375 A>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr23:1401599 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:37331725 C>T maps to ENST00000262825 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr22:37329986 C>T maps to ENST00000262825 N428N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr22:37334017 C>G maps to ENST00000262825 S729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr17:38172832 G>A maps to NM_000759.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr17:38173106 C>T maps to NM_000759.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:36941191 C>T maps to NM_156039.3 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:36933438 C>T maps to NM_156039.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:36932896 G>T maps to NM_156039.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr1:36933214 G>A maps to NM_156039.3 G634G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:19316070 G>T maps to NM_018371.4 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr8:19277863 C>G maps to NM_018371.4 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr8:19297441 C>T maps to NM_018371.4 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr10:43662479 C>T maps to NM_018590.3 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr10:43659400 G>A maps to NM_018590.3 W356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr17:61972838 C>T maps to NM_001317.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr17:61949640 G>A maps to NM_020991.3 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr17:61950571 C>T maps to NM_020991.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr17:61950661 G>T maps to NM_020991.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr17:61988189 A>G maps to NM_022579.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:75094077 C>T maps to NM_004383.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr15:75093864 G>A maps to NM_004383.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr15:75094381 C>G maps to NM_004383.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr15:75094381 C>G maps to NM_004383.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr8:3224563 G>T maps to NM_033225.5 I1035I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr8:2830726 G>T maps to NM_033225.5 S2945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:4851875 C>T maps to NM_033225.5 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:2944669 G>A maps to NM_033225.5 R2475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:3047536 G>A maps to NM_033225.5 F1765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr8:2944709 A>T maps to NM_033225.5 P2461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:3009030 G>T maps to NM_033225.5 T1973T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr8:2824090 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr8:3265697 T>A maps to NM_033225.5 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr8:3087571 A>T maps to NM_033225.5 P1445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr1:34258085 G>T maps to ENST00000373381 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr1:34166270 A>C maps to ENST00000373381 V1153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:34042989 G>A maps to ENST00000373381 N2454N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:34015930 C>T maps to ENST00000373381 P2881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:34003078 G>A maps to ENST00000373381 C3214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr1:34204786 C>T maps to ENST00000373381 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr1:34166204 C>T maps to ENST00000373381 V1175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:33988999 A>G maps to ENST00000373381 D3432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr1:34037225 G>A maps to ENST00000373381 I2581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:33987120 G>A maps to ENST00000373381 F3473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr1:34038270 C>A maps to ENST00000373381 E2493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr1:34208905 C>T maps to ENST00000373381 K676K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:34180298 G>T maps to ENST00000373381 G1058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:33990620 C>T maps to ENST00000373381 K3379K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:34068018 G>A maps to ENST00000373381 L2180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr1:34191064 C>T maps to ENST00000373381 G820G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr1:34046410 G>T maps to ENST00000373381 Y2403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr1:34191067 G>A maps to ENST00000373381 I819I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr1:34089024 C>A maps to ENST00000373381 S1849S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:34164409 G>A maps to ENST00000373381 L1250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:34090667 G>C maps to ENST00000373381 S1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:34554656 G>A maps to ENST00000373381 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr8:113318248 G>T maps to NM_198123.1 T2686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr8:113678639 T>A maps to NM_198123.1 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:113308173 T>C maps to NM_198123.1 G2834G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr8:113529361 G>A maps to NM_198123.1 Q1553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr8:113348980 G>A maps to NM_198123.1 Q2307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:113518954 G>A maps to NM_198123.1 V1620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:113267561 A>G maps to NM_198123.1 F3319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:113649123 G>A maps to NM_198123.1 R1213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr8:113678549 C>G maps to NM_198123.1 V924V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr8:114290866 G>C maps to NM_198123.1 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr8:113241089 G>T maps to NM_198123.1 S3620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr8:113529419 G>A maps to NM_198123.1 V1533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr8:114327002 A>T maps to NM_198123.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr8:113299302 T>C maps to NM_198123.1 P3107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr8:113308060 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr8:113364670 G>A maps to NM_198123.1 Q2077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr8:113649140 G>C maps to NM_198123.1 S1207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr8:113304928 A>G maps to NM_198123.1 C2875C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr8:113516207 T>A did not map to a codon.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr8:113347651 G>A maps to NM_198123.1 T2357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr8:113275982 G>A maps to NM_198123.1 F3249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:70810684 G>T maps to NM_001890.1 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr4:70810653 G>A maps to NM_001890.1 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr13:37678382 G>A maps to NM_145203.5 N337N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr17:80210376 C>T maps to NM_001893.3 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr17:80223619 T>C maps to NM_001893.3 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:80223667 C>T maps to NM_001893.3 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr22:38694853 G>A maps to NM_001894.4 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr22:38694856 G>A maps to NM_001894.4 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr22:38695939 C>T maps to NM_001894.4 K232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr22:38695942 C>T maps to NM_001894.4 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr15:64496767 G>A maps to NM_022048.3 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:1978736 C>T maps to NM_001319.6 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr19:1978611 C>T maps to NM_001319.6 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:1969890 G>A maps to NM_001319.6 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:1978448 C>T maps to NM_001319.6 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr19:1978724 G>C maps to NM_001319.6 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr5:122923804 C>T maps to NM_001044723.1 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr5:122881388 C>G maps to NM_001044723.1 S11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr5:122881417 C>T maps to NM_001044723.1 R21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr20:472990 C>T maps to NM_177559.2 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:58201600 G>A maps to NM_001896.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr6:31637173 C>G maps to ENST00000375885 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr15:75977187 C>T maps to NM_001897.4 L1446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr15:75968127 G>A maps to NM_001897.4 F2244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr15:75981329 G>A maps to NM_001897.4 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr15:75969359 G>A maps to NM_001897.4 Q1834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr3:47619227 G>A maps to ENST00000383738 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr3:47604193 C>A maps to ENST00000383738 E533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr8:68044191 G>A maps to ENST00000389042 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr8:68044263 G>A maps to ENST00000389042 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr8:68071327 C>T maps to ENST00000389042 Q862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr8:68044209 G>C maps to ENST00000389042 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr8:67976689 A>G maps to ENST00000389042 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr3:39185626 C>A did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr12:51467661 G>A maps to NM_030809.1 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:51467851 C>T maps to NM_030809.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr12:51461710 G>C maps to NM_030809.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:166535683 C>T maps to ENST00000409420 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr2:166533035 C>G maps to ENST00000409420 S240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:18162454 C>T maps to NM_020536.4 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr20:18163826 G>A maps to NM_020536.4 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr20:18142469 C>G maps to NM_020536.4 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr11:19209780 G>A maps to NM_003476.3 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr20:23433218 A>G did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr20:23614617 G>A maps to NM_000099.2 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr20:23614618 G>A maps to NM_000099.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr20:23667808 G>A maps to NM_001899.2 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr20:23472336 C>T maps to NM_005492.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr20:23586271 C>T maps to NM_001008693.2 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr20:23549012 C>T maps to NM_080610.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr20:23546709 A>G maps to NM_080610.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr20:23545585 C>T maps to NM_080610.2 *148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr23:100086568 C>A did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr23:100086637 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr23:100088251 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:100086631 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:100087721 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:100087777 G>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr10:53458568 C>A maps to NM_015235.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr10:53458274 G>C maps to NM_015235.2 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr10:53459150 C>T maps to NM_015235.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr23:134947459 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr23:120008770 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:120009115 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr23:120008747 A>T did not map to a codon.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr23:120009126 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr23:120009215 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr23:120009424 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr23:153880626 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:153880853 C>T did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr23:153880681 C>G did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr23:153880693 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:19996001 T>C maps to NM_172241.2 Q591Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr18:19996232 G>A maps to NM_172241.2 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr18:19997161 G>A maps to NM_172241.2 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr18:19996427 T>C maps to NM_172241.2 E449E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr14:39783994 C>T maps to ENST00000396158 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr6:132032136 G>T maps to NM_001145659.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr6:132030915 C>T maps to NM_001145659.1 E414E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:126691535 G>A maps to NM_022802.2 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:126683151 G>A maps to NM_022802.2 G762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr10:126682515 G>A maps to NM_022802.2 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr10:126727601 T>A maps to NM_001083914.1 K8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:85036400 G>C maps to NM_004388.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:67662355 G>A maps to NM_006565.3 Q534Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:67671649 G>T maps to NM_006565.3 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:67670645 G>T maps to NM_006565.3 E631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr16:67645083 C>T maps to NM_006565.3 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:67645044 G>T maps to NM_006565.3 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr16:67662346 C>A maps to NM_006565.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:67670707 G>C maps to NM_006565.3 R651R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr16:67645211 T>C maps to NM_006565.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr16:67654638 G>T maps to NM_006565.3 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr20:56093884 G>A maps to ENST00000423479 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr20:56098313 C>T maps to ENST00000423479 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr18:77472970 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr2:219268014 C>T maps to NM_021198.1 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:58217462 C>T maps to NM_005730.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr15:44788617 G>A maps to NM_016396.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr16:30910756 C>G maps to NM_001330.3 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:70877217 C>T maps to NM_001902.5 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr8:104394803 C>T maps to NM_138455.2 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr8:104388152 C>G maps to NM_138455.2 S113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr8:104388120 G>A maps to NM_138455.2 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr8:104388096 G>A maps to NM_138455.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:204736143 T>G maps to NM_005214.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr5:138266173 C>T maps to ENST00000355078 Q675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr2:79971688 A>T maps to ENST00000402739 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr2:80801300 C>T maps to ENST00000402739 F585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:80646671 G>A maps to ENST00000402739 K412K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:80620373 G>A maps to ENST00000402739 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr2:80772154 T>C maps to ENST00000402739 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:80782935 C>T maps to ENST00000402739 I553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr2:80101254 G>A maps to ENST00000402739 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr2:80773033 C>T maps to ENST00000402739 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr2:79971664 C>G maps to ENST00000402739 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr2:80801294 A>G maps to ENST00000402739 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr2:80808943 G>A maps to ENST00000402739 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr2:80782945 G>T maps to ENST00000402739 E557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr2:80085163 C>T maps to ENST00000402739 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:68040317 C>T maps to NM_013266.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:69366617 C>A maps to NM_013266.2 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr10:69281695 G>C maps to NM_013266.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr10:68979429 G>A maps to NM_013266.2 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr10:68535252 C>T maps to NM_013266.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:111741737 C>T maps to NM_003798.2 E308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr9:111745481 C>T maps to NM_003798.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr20:36488326 C>T maps to NM_030877.3 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr20:36468595 G>T maps to NM_030877.3 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr11:57571090 A>G did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:57569393 C>G maps to NM_001085458.1 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr11:57575891 C>T maps to NM_001085458.1 Q708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:11098860 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr5:11117570 G>A maps to NM_001332.2 I756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr5:11082892 G>T maps to NM_001332.2 L901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr5:11022942 C>T maps to NM_001332.2 K979K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr5:11199686 C>T maps to NM_001332.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr5:10981932 C>T maps to NM_001332.2 L1123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr5:11346668 G>A maps to NM_001332.2 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr5:11022900 G>A maps to NM_001332.2 I993I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr5:11397271 T>C maps to NM_001332.2 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr5:11397262 C>A maps to NM_001332.2 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr5:11346601 G>A maps to NM_001332.2 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr17:3560052 C>T maps to NM_001031681.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:41450571 C>T maps to NM_001905.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr1:41466747 C>T maps to NM_001905.2 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:41475889 G>T maps to NM_001905.2 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:16707721 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:16657273 T>C did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr23:16711296 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr23:16627767 A>T did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:16701232 T>C did not map to a codon.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr8:11710939 G>A maps to NM_147783.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr11:88027635 G>A maps to NM_001814.4 Y310Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:1780809 G>A maps to NM_001909.3 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr11:1774825 G>A maps to NM_001909.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr11:66332277 C>T did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr14:25044607 G>A maps to NM_001911.2 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr14:25043946 C>T maps to NM_001911.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr14:25045380 C>A maps to NM_001911.2 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr14:25043979 C>T maps to NM_001911.2 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr15:79224773 G>A maps to NM_004390.3 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr15:79220066 G>A maps to NM_004390.3 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:79224764 A>T maps to NM_004390.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr1:150772125 C>T maps to NM_000396.3 E226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:99795231 C>T maps to NM_001333.2 *335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr9:99795260 G>A maps to NM_001333.2 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:156864397 G>A maps to NM_001334.2 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:156850778 T>C maps to NM_001334.2 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:150722491 G>T maps to NM_004079.4 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:150724421 C>T maps to NM_004079.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr11:65649733 G>A maps to NM_001335.3 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr20:57581449 G>A maps to NM_001336.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr20:57581416 G>A maps to NM_001336.3 C89C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr11:70281228 C>T maps to NM_005231.3 Y538Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr11:70255948 G>C maps to NM_001184740.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr11:70269091 G>A maps to NM_001184740.1 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr11:70279316 G>A maps to NM_001184740.1 Q422Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:70277331 G>C maps to NM_001184740.1 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr11:70266504 G>C did not map to a codon.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr7:117407113 C>G maps to NM_033427.2 L965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr7:117400555 C>T maps to NM_033427.2 V1035V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:117431346 G>A maps to NM_033427.2 Q635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr7:117351648 G>C maps to NM_033427.2 S1645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr7:117385903 T>A maps to NM_033427.2 L1172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:112998770 A>G maps to NM_018704.2 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:112998575 G>A maps to NM_018704.2 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:112998803 G>A maps to NM_018704.2 Q230Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr19:51602193 G>A maps to NM_145232.3 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr19:51607325 G>A maps to NM_145232.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr16:88779731 C>A maps to ENST00000378384 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:126993381 C>T maps to NM_001048252.2 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr10:16967340 G>C maps to NM_001081.3 S2182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr10:17083211 C>T maps to NM_001081.3 E1279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr10:16911659 C>T maps to NM_001081.3 W3143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr10:17088053 G>A maps to NM_001081.3 F1123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr10:16994308 C>T maps to NM_001081.3 Q1645Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr10:17110769 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr10:16932502 C>G maps to NM_001081.3 V2874V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr10:16990555 G>A maps to NM_001081.3 S1710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr10:16883019 C>T maps to NM_001081.3 A3230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr10:16878249 G>A maps to NM_001081.3 F3388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr10:16916383 C>T maps to NM_001081.3 V3075V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr10:17083184 A>G maps to NM_001081.3 Y1288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr10:16893287 T>A maps to NM_001081.3 T3203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr10:16957094 C>T maps to NM_001081.3 R2429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr10:16970189 T>A maps to NM_001081.3 V2079V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr10:16967369 A>G maps to NM_001081.3 N2172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr10:17110612 C>A maps to NM_001081.3 E928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr10:17147548 G>C maps to NM_001081.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr10:17145192 G>A maps to NM_001081.3 Y487Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr10:17113579 C>A maps to NM_001081.3 E824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr10:17113559 A>G maps to NM_001081.3 P830P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr10:17113831 G>A maps to NM_001081.3 Q814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr10:16975233 G>A maps to NM_001081.3 F1992F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:55950042 G>A maps to NM_017949.1 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr17:55950146 C>A maps to NM_017949.1 G221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:55962591 C>A maps to NM_017949.1 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr17:55962826 G>C maps to NM_017949.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:148457546 G>T maps to NM_003592.2 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr7:148481097 C>T maps to NM_003592.2 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:148489831 G>A maps to NM_003592.2 Q607Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr7:148457437 G>C maps to NM_003592.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:35317793 G>A maps to NM_001198778.1 Q540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr10:35333783 T>A maps to NM_001198778.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr10:35320308 G>C maps to NM_001198778.1 Y454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr10:35317751 T>A maps to NM_001198778.1 K554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr10:35320463 G>A maps to NM_001198778.1 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr10:35318556 A>C maps to NM_001198778.1 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr10:35360126 G>T maps to NM_001198778.1 S59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:113893834 G>T maps to NM_001008895.1 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr13:113893792 G>A maps to NM_001008895.1 Q321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr13:113897469 G>A maps to NM_001008895.1 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr23:119694329 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:119669774 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr23:119670867 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr23:119691809 G>A did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:119670882 G>A did not map to a codon.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr23:119691788 T>A did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:119694178 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:119694218 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr23:119673228 T>G did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr11:107925383 T>C maps to NM_003478.3 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr11:107917092 G>A maps to NM_003478.3 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr6:43006202 G>C maps to NM_001168370.1 L1609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr6:43011252 G>A maps to NM_001168370.1 L1180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr6:43012600 C>A maps to NM_001168370.1 E1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:43020304 G>T maps to NM_001168370.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr6:43014800 C>T maps to NM_001168370.1 V822V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr6:43012595 C>T maps to NM_001168370.1 Q1106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr6:43008414 G>A maps to NM_001168370.1 I1376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr6:43174207 C>T maps to ENST00000354495 F1724F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:43190339 C>T maps to ENST00000354495 F2331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr6:43152560 C>A maps to ENST00000354495 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:43156451 A>C maps to ENST00000354495 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr6:43189452 C>T maps to ENST00000354495 F2261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr6:43189467 C>T maps to ENST00000354495 L2266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:43172786 C>T maps to ENST00000354495 F1522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr6:43173107 C>T maps to ENST00000354495 P1580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr6:43188498 C>G maps to ENST00000354495 L2146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:43171252 C>G maps to ENST00000354495 L1316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:33385310 G>A maps to NM_001014433.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr7:101877353 C>T maps to ENST00000360264 T1163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr7:101882762 G>T maps to ENST00000360264 A1273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:111655741 G>T did not map to a codon.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr12:111748049 G>A maps to NM_015267.3 E488E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FH-01A-11D-A38G-08 chr12:111758431 G>A maps to NM_015267.3 P873P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr12:111758092 G>T maps to NM_015267.3 P760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr12:111758152 C>T maps to NM_015267.3 G780G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr12:111758221 G>A maps to NM_015267.3 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr12:111785573 G>A maps to NM_015267.3 Q1302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr12:111785411 G>A maps to NM_015267.3 P1248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr10:124594531 G>A maps to NM_022034.4 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr2:180819033 G>A maps to NM_020943.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:64267617 G>A maps to NM_005869.2 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr5:64267636 C>T maps to NM_005869.2 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr5:64096130 C>T maps to NM_005869.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:107197721 C>A maps to NM_152434.2 E867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr4:48993958 C>T maps to NM_025087.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:49052779 C>T maps to NM_025087.2 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr4:49052743 G>T maps to NM_025087.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr4:48996747 C>T maps to NM_025087.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr4:49052779 C>T maps to NM_025087.2 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr16:57406488 G>A maps to NM_002996.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr3:39307646 G>A maps to NM_001171174.1 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:39306962 C>T maps to NM_001171174.1 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:39307061 A>G maps to NM_001171174.1 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:18931334 G>T maps to NM_001338.3 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr21:18933791 C>T maps to NM_001338.3 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr21:18919366 C>A maps to NM_001338.3 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr4:74735631 C>G maps to NM_001511.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr4:74735434 G>A maps to NM_001511.2 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr4:76956235 T>A maps to NM_005409.4 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:78527048 C>T maps to NM_006419.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr5:134910272 G>A maps to NM_004887.4 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr17:4642108 C>G maps to NM_001100812.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:74964334 G>A maps to NM_002089.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr4:74863802 C>T maps to NM_002994.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr4:74702931 G>A maps to NM_002993.3 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr2:219029262 G>A maps to NM_000634.2 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr2:219028977 G>A maps to NM_000634.2 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr23:70836459 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:70836317 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr23:70837222 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr23:70837174 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr11:118764411 C>T maps to NM_001716.3 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:45988916 C>A maps to NM_006564.1 S315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr2:237489980 C>T maps to NM_020311.2 H291H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr18:47811485 G>A maps to NM_001101654.1 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr4:105412308 G>A maps to NM_025212.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr4:105412050 C>T maps to NM_025212.1 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr23:144909202 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr23:144909441 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr23:30577603 C>T did not map to a codon.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr23:30578310 G>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr23:35984702 C>G did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:36007618 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr23:35959431 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr23:35993360 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:35988962 G>T did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:35974112 G>A did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:36007599 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:35974280 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:35970071 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr23:35989824 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr23:35984767 A>T did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr23:19947929 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr23:19973575 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr23:19973520 G>A did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr23:19983509 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:19971994 G>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:19984477 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:19984594 G>A did not map to a codon.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr23:75393482 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr23:75396808 G>A did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr23:45010957 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:45017018 G>A did not map to a codon.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr23:45010991 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:45051119 G>C did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr23:40496395 G>A did not map to a codon.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr23:40506338 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr23:40506715 C>A did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr23:40498280 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:40506724 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:40506389 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr23:148628333 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr23:149102007 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:106456209 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr23:134294476 C>A did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:118675314 C>G did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:118675340 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr23:118676490 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr23:105855595 G>T did not map to a codon.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr23:105855562 G>T did not map to a codon.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr23:105881035 T>C did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr23:105882903 C>A did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:105912461 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:105912469 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:105855500 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr23:105921469 T>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr23:23956727 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr23:23957399 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr23:23929920 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr23:36091314 C>G did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:36091419 T>G did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:36089991 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr23:36156471 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr23:115593126 C>G did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr23:70324222 C>A did not map to a codon.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr23:70325930 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr23:139040373 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr23:139038602 C>T did not map to a codon.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr23:139038361 G>C did not map to a codon.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr23:139047627 A>G did not map to a codon.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr23:139038287 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:61514722 G>T maps to NM_001915.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:50391173 G>C maps to NM_007022.3 *223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr3:50390808 C>G maps to NM_007022.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr3:50391054 C>T maps to NM_007022.3 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr16:69458657 C>T maps to NM_030579.2 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:7761958 G>A maps to NM_144607.4 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:7761742 C>T maps to NM_144607.4 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr17:7762001 C>T maps to NM_144607.4 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:202935921 G>C maps to NM_016243.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:202935954 C>T maps to NM_016243.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:84618804 G>A maps to NM_016230.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:54656536 G>A maps to NM_001031672.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr16:88717387 C>A maps to NM_000101.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr23:37664366 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:37653049 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:145151086 C>T maps to NM_001916.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr8:145151129 G>T maps to NM_001916.3 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr7:25163442 C>T maps to NM_018947.5 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr15:22933810 C>T maps to NM_014608.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr15:22929847 G>A maps to NM_014608.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr15:22990157 C>T maps to NM_014608.2 I926I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr15:22929847 G>A maps to NM_014608.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr15:22925787 G>T maps to NM_014608.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:22993124 C>T maps to NM_014608.2 I1004I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr15:22990181 G>A maps to NM_014608.2 L934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr15:22925811 G>A maps to NM_014608.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr15:22935924 G>A maps to NM_014608.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr5:156714071 G>T maps to ENST00000442283 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr5:156786152 C>T maps to ENST00000442283 S963S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr5:156721802 G>T maps to ENST00000442283 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr5:156721803 G>T maps to ENST00000442283 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47W-01A-11D-A23U-08 chr17:74533612 C>T maps to NM_134268.3 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr17:74527170 G>A maps to NM_134268.3 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr8:145690203 C>T maps to NM_138496.1 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr8:145689920 G>A maps to NM_138496.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr8:145689767 G>A maps to NM_001129888.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:83127892 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:83126561 C>T did not map to a codon.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr23:83128556 A>G did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr23:83128695 A>G did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:83128355 C>A did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr23:83129106 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr16:50825576 C>T maps to ENST00000311559 I739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr16:50821712 G>A maps to ENST00000311559 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr15:74640359 G>A maps to NM_000781.2 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr8:143960497 G>T maps to ENST00000377675 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:51514602 G>A maps to NM_031226.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr15:75014649 C>T maps to NM_000499.3 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr15:75014949 C>T maps to NM_000499.3 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr15:75042615 G>C maps to NM_000761.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr15:75042594 G>C maps to NM_000761.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:38302447 C>T maps to NM_000104.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:38297912 G>T maps to NM_000104.3 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr2:204131391 G>A maps to ENST00000429815 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr20:52775662 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:52788163 T>C maps to NM_000782.4 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr20:52774034 C>T maps to NM_000782.4 Q442Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr20:52788148 C>A maps to NM_000782.4 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr20:52789518 C>T maps to NM_000782.4 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr20:52790073 C>T maps to NM_000782.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr2:72361940 G>A maps to NM_019885.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:72359631 C>T maps to NM_019885.2 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr10:94821037 G>A maps to NM_183374.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr10:94828375 C>T maps to NM_183374.2 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr2:219647115 C>T maps to NM_000784.3 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr2:219679422 C>G maps to NM_000784.3 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr2:219674350 C>T maps to NM_000784.3 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr2:219647115 C>T maps to NM_000784.3 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:219647123 C>T maps to NM_000784.3 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr2:219677004 G>A maps to NM_000784.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:58158584 C>T maps to NM_000785.3 Q305Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:41596469 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr19:41600898 G>A maps to NM_000766.3 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr19:41600940 C>T maps to NM_000766.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr19:41600884 C>T maps to NM_000766.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr19:41354267 G>A maps to NM_000762.5 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:41349838 G>A maps to NM_000762.5 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:41354575 C>A maps to NM_000762.5 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:41351240 T>C maps to NM_000762.5 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:41351936 G>A maps to NM_000762.5 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr19:41386395 G>T maps to NM_000764.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:41388064 C>G maps to NM_000764.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr19:41383190 C>A maps to NM_000764.2 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:41386405 G>T maps to NM_000764.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr19:41518595 C>G maps to NM_000767.4 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:41522599 C>A maps to NM_000767.4 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr19:41515945 C>T maps to NM_000767.4 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:41515939 C>T maps to NM_000767.4 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:41518643 C>T maps to NM_000767.4 D406D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr10:96602691 G>T maps to NM_000769.1 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr10:96827443 G>C maps to NM_000770.3 S58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr10:96829100 C>T maps to NM_000770.3 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr10:96805591 G>A maps to NM_000770.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr10:96824613 G>A maps to NM_000770.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:96698471 C>G maps to NM_000771.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr10:96702000 C>T maps to NM_000771.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr22:42523514 G>A maps to NM_000106.4 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr22:42524896 C>G maps to NM_000106.4 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr22:42524797 G>T maps to NM_000106.4 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr10:135350732 C>T maps to NM_000773.3 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr10:135352446 C>G maps to NM_000773.3 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr10:135342013 G>A maps to NM_000773.3 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr19:41631522 C>T maps to NM_000774.3 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:41633860 C>A maps to NM_000774.3 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:41626321 C>T maps to NM_000774.3 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:41633920 G>A maps to NM_000774.3 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr19:41712221 G>A maps to ENST00000301173 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr19:41704392 C>T maps to ENST00000301173 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:41709439 C>T maps to ENST00000301173 D354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr19:41704735 G>A maps to ENST00000301173 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:1024673 G>A maps to NM_017781.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr6:46607285 C>A maps to NM_016593.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:99364027 C>T maps to NM_017460.3 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr7:99367795 C>T maps to NM_017460.3 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:99453288 T>A maps to NM_022820.3 L249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr7:99441831 G>A maps to NM_022820.3 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr7:99459390 G>A maps to NM_022820.3 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr7:99247764 G>C maps to NM_000777.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr7:99264652 G>A maps to NM_000777.3 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr7:99247764 G>C maps to NM_000777.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:99332707 G>C maps to ENST00000292414 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr7:99312264 A>G maps to ENST00000292414 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr7:99312306 T>C did not map to a codon.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr7:99308459 A>C maps to ENST00000292414 Y307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:99319921 C>T maps to ENST00000292414 W72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:100165801 G>T did not map to a codon.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr14:100187617 C>A maps to NM_006668.1 Y341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr14:100166435 G>C maps to NM_006668.1 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr1:47407090 C>G maps to ENST00000371904 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:47401192 A>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:47406952 G>A maps to ENST00000371904 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:47406994 G>A maps to ENST00000371904 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr1:47610598 C>T maps to NM_001010969.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:47610565 C>G maps to NM_001010969.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:47610072 G>T maps to NM_001010969.2 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr1:47614297 C>T maps to NM_001010969.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr1:47603336 C>T maps to NM_001010969.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:47609469 G>A maps to NM_001010969.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:47280780 C>G maps to NM_001099772.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr19:16038027 G>A maps to NM_021187.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr19:16045053 C>T maps to NM_021187.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr19:15784509 G>A maps to NM_023944.2 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:15806820 C>T maps to NM_023944.2 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr19:15806827 C>T maps to NM_023944.2 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:15794527 C>G maps to NM_023944.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:15794548 C>T maps to NM_023944.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:15794548 C>T maps to NM_023944.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr19:16000452 G>C maps to NM_001082.3 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:16001183 G>A maps to NM_001082.3 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr19:15989724 G>A maps to NM_001082.3 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:15648196 C>T maps to NM_173483.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:15662125 C>T maps to NM_173483.3 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr19:15648777 C>G maps to NM_173483.3 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr19:15760758 C>T maps to NM_000896.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr19:15730299 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:15734172 C>T maps to NM_007253.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:15728815 T>G maps to NM_007253.3 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:15734073 C>G maps to NM_007253.3 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr19:15739219 C>T maps to NM_007253.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:15728929 C>A maps to NM_007253.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr19:15728950 C>T maps to NM_007253.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:187130376 C>T maps to ENST00000511608 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr1:47497106 G>T did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:47501794 C>T maps to NM_178033.1 Q243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:47564902 G>A maps to NM_178134.2 Q338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr1:47548039 G>A maps to NM_178134.2 W133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47S-01A-11D-A23U-08 chr7:91747926 G>C maps to NM_000786.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr8:59404264 G>A maps to NM_000780.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr8:59410874 G>A maps to NM_000780.3 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr8:59409362 C>T maps to NM_000780.3 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr8:59409281 G>T maps to NM_000780.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr8:59409401 G>T maps to NM_000780.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr8:65527622 G>A maps to NM_004820.3 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr3:42915943 C>A maps to NM_004391.2 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:42916915 C>G maps to NM_004391.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr3:42917104 G>A maps to NM_004391.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:86048267 G>A maps to NM_001554.4 E268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:86047887 C>T maps to NM_001554.4 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:86047953 G>A maps to NM_001554.4 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:86047729 C>T maps to NM_001554.4 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:86047752 C>T maps to NM_001554.4 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr23:77528396 G>A did not map to a codon.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr13:49281954 C>T maps to NM_020377.2 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr13:49281756 C>T maps to NM_020377.2 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr7:6210830 A>C did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:6227346 C>T maps to ENST00000396741 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:6227352 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr7:6210577 G>A maps to ENST00000396741 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr7:6227306 G>A maps to ENST00000396741 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr22:37699295 C>T maps to NM_013385.3 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr2:158272446 G>A maps to NM_004288.4 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr22:24759249 C>A maps to NM_015330.2 S922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr22:24761540 G>A maps to NM_015330.2 Q975Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:24709366 A>C maps to NM_015330.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr22:24730512 C>T maps to NM_015330.2 L844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:20013765 G>A maps to NM_001033553.1 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr17:20200323 C>T maps to NM_001033553.1 F997F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr17:20108963 C>A maps to NM_001033553.1 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr21:27840902 A>G maps to ENST00000435845 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr4:4393203 G>C maps to NM_001040101.1 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr14:59814259 G>A maps to NM_014992.1 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr14:59782053 C>G maps to NM_014992.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr14:59798178 C>T maps to NM_014992.1 Q605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:39846246 G>A maps to ENST00000398904 K476K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:39867938 C>T maps to ENST00000398904 F922F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr6:39847177 C>T maps to ENST00000398904 D590D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr6:39847132 C>T maps to ENST00000398904 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr6:39846178 G>A did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:57481003 C>A maps to ENST00000371231 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:57491700 C>A maps to ENST00000371231 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:57480628 G>A maps to ENST00000371231 D490D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:57489207 G>A maps to ENST00000371231 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr5:39381583 A>T maps to NM_001343.2 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr5:39377091 A>G maps to NM_001343.2 F599F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr5:39377347 C>T maps to NM_001343.2 W514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr9:124535707 G>A maps to ENST00000408936 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr9:124441050 C>T maps to ENST00000408936 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr13:72440380 G>C maps to ENST00000359684 S176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:72134057 G>T maps to ENST00000359684 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr13:72053448 C>T did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr13:72053439 C>T maps to ENST00000359684 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr13:72146981 G>C maps to ENST00000359684 S484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr23:85403940 T>A did not map to a codon.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr23:85969635 G>A did not map to a codon.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr14:59113770 C>G maps to NM_016651.5 V810V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr14:59111979 C>A maps to NM_016651.5 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr14:59112714 A>T maps to NM_016651.5 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:47151861 T>C maps to NM_145056.2 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:49569107 T>C maps to NM_004393.4 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr11:61495695 C>T maps to NM_006133.2 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr11:61511591 C>T maps to NM_006133.2 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr11:61505218 C>A maps to NM_006133.2 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr11:61507076 C>T maps to NM_006133.2 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr11:61503821 G>A maps to NM_006133.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr11:61504667 A>G maps to NM_006133.2 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:61508656 G>T maps to NM_006133.2 G669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr11:61506959 C>G maps to NM_006133.2 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr7:6456352 G>A maps to NM_139179.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr7:6472551 G>A maps to NM_139179.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:6476108 G>A maps to NM_139179.3 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr7:6476041 G>A maps to NM_139179.3 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:6487434 G>T maps to NM_139179.3 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr7:6472521 G>A maps to NM_139179.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr11:61106843 C>T maps to NM_015533.3 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr11:61111326 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr11:61113950 C>T maps to NM_015533.3 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr11:61110062 G>A maps to NM_015533.3 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr3:49053870 T>G maps to NM_001009996.1 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:49054899 T>C maps to NM_001009996.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr3:49053758 C>G maps to NM_001009996.1 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr3:49055096 C>A maps to NM_001009996.1 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr3:49053091 G>A maps to NM_001009996.1 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr19:13080798 G>A did not map to a codon.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr12:109292481 C>T maps to NM_001917.4 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:155699108 C>T maps to NM_004632.3 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:90283583 C>T maps to NM_004938.2 R666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr9:90262308 G>T maps to NM_004938.2 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:90266557 C>T maps to NM_004938.2 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr9:90318017 C>G maps to NM_004938.2 P982P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:64332446 G>C maps to NM_014326.3 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr19:3964260 G>A maps to NM_001348.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:3964646 G>A maps to NM_001348.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr19:3959236 G>A maps to NM_001348.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:100756842 C>T maps to NM_014395.2 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:159175889 T>C maps to NM_001122951.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:159175831 G>A maps to NM_001122951.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:136743011 C>T maps to NM_001349.2 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:136700953 A>C maps to NM_001349.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr2:136673797 C>T maps to NM_001349.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr1:173806134 C>T maps to NM_018122.4 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:173819575 G>T maps to NM_018122.4 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr6:33287434 C>T maps to NM_001350.4 E554E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr6:33289242 C>T maps to NM_001350.4 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr6:33289287 G>C maps to NM_001350.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr6:33286788 C>T maps to NM_001350.4 R716R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr6:33288741 G>A maps to NM_001350.4 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr6:33288585 G>A maps to NM_001350.4 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:1432625 C>T maps to NM_018959.2 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr19:1434777 C>G maps to NM_018959.2 S364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr19:1425925 C>A maps to NM_018959.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr19:1434777 C>G maps to NM_018959.2 S364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:51634656 C>T maps to NM_014764.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:121929415 C>T maps to NM_014618.2 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:121930183 C>T maps to NM_014618.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr9:121929759 G>A maps to NM_014618.2 R630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr9:121929439 G>A maps to NM_014618.2 I736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr9:121929393 G>A maps to NM_014618.2 Q752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr9:121929628 C>A maps to NM_014618.2 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:87530129 G>A maps to NM_006716.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr7:87506067 G>A maps to NM_006716.3 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr17:42828542 C>T maps to NM_145663.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr9:136501510 C>G maps to NM_000787.3 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:136507467 C>G maps to NM_000787.3 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:136501792 C>G maps to NM_000787.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr9:136501717 G>A maps to NM_000787.3 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr2:120128373 G>C maps to NM_001178017.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FM-01A-11D-A38G-08 chr5:176887531 G>T maps to ENST00000393565 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr7:44100406 G>A maps to NM_001122956.1 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:44100394 C>T maps to NM_001122956.1 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr7:44091444 G>A maps to NM_001122956.1 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr3:137888978 C>G maps to NM_016216.3 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:137885985 G>C maps to NM_016216.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr3:137893536 A>T maps to NM_016216.3 L34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr3:137882264 G>A maps to NM_016216.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr1:100701033 G>C maps to NM_001918.2 S70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr11:20180779 G>A maps to ENST00000227256 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr11:20181519 G>A maps to ENST00000227256 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr11:20178182 C>T maps to ENST00000227256 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:20178726 C>T maps to ENST00000227256 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr12:45429831 G>T maps to NM_001004329.2 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr12:45417648 T>G maps to NM_001004329.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr14:24590580 G>A maps to NM_025230.4 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr9:34088416 C>T maps to NM_015397.3 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr9:34088356 G>T maps to NM_015397.3 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr9:34126362 G>A maps to NM_015397.3 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr23:125686548 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr23:125685221 T>G did not map to a codon.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr23:125686322 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr23:125685953 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr23:125685910 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:125685765 C>A did not map to a codon.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr23:125685906 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:125686552 C>T did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr23:125686234 C>T did not map to a codon.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr23:125686242 A>G did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:125685667 A>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:125686426 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr23:125298898 G>A did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr23:125299170 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:125299589 C>A did not map to a codon.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr23:125298728 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr23:125299663 T>A did not map to a codon.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr23:125299120 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:125299412 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr23:125298920 G>A did not map to a codon.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr23:125299270 G>T did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:125299260 G>T did not map to a codon.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr23:125299407 C>T did not map to a codon.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr23:125298847 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr23:125299029 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr23:125299767 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr8:104427571 T>C maps to NM_015420.6 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr8:104427283 G>A maps to NM_015420.6 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr8:104438288 T>G maps to NM_015420.6 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:14066958 C>T maps to NM_138353.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr19:14070851 C>T maps to NM_138353.2 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr19:14065240 C>G maps to NM_138353.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:14065246 A>C maps to NM_138353.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr2:172334510 C>G maps to NM_025000.3 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:172306413 G>T maps to NM_025000.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr2:172291690 C>T maps to NM_025000.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr14:73404760 C>G maps to NM_015604.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr14:73412590 G>C did not map to a codon.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr4:41984467 C>G maps to NM_001029955.3 S220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr4:41984424 C>T maps to NM_001029955.3 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:88885229 C>A maps to NM_152418.3 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr8:88885583 G>A maps to NM_152418.3 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr8:88885179 G>A maps to NM_152418.3 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr8:88885073 G>A maps to NM_152418.3 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr14:69583207 G>A maps to NM_003861.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:168014276 G>A maps to ENST00000367840 Q690Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:167906232 G>A maps to ENST00000367840 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr17:61628118 G>T maps to NM_005828.3 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr1:160187419 C>A maps to NM_015726.3 E586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:160209812 C>A maps to NM_015726.3 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr23:27997888 T>A did not map to a codon.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr23:27999130 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:27997801 G>T did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr23:27999089 G>T did not map to a codon.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr23:27998067 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr23:27998744 C>A did not map to a codon.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr23:27999222 C>T did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr23:27998203 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:27999384 G>T did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr23:27998164 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr23:27998289 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr23:27766059 C>G did not map to a codon.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr23:27766625 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:27766830 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:27766327 C>G did not map to a codon.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr23:27766598 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr23:27766665 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr6:117866678 C>T maps to ENST00000338728 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:98538213 G>A maps to ENST00000326857 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr3:98600543 C>T maps to ENST00000326857 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr3:98538241 C>T maps to ENST00000326857 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:98526974 G>T maps to ENST00000326857 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr18:50278526 C>T maps to NM_005215.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr18:50450131 C>A maps to NM_005215.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr18:50976987 C>T maps to NM_005215.3 I1116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr18:50866203 T>C maps to NM_005215.3 Y762Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr18:51013254 G>A maps to NM_005215.3 P1275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr18:50450224 C>G maps to NM_005215.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr18:50705335 C>A maps to NM_005215.3 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr18:50731613 G>A maps to NM_005215.3 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr11:31327781 G>A maps to NM_181807.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:24175046 G>A maps to NM_016356.3 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr6:24302031 G>A maps to NM_016356.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr6:24205301 C>T maps to NM_016356.3 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr6:24174966 G>A maps to NM_016356.3 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr1:32676908 G>A maps to NM_001099434.1 K101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:6661248 C>A maps to NM_003737.2 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr11:6643189 G>A maps to NM_003737.2 I3239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:6648800 C>G maps to NM_003737.2 L1823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:6653795 G>A maps to NM_003737.2 R983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr11:6652343 T>A maps to NM_003737.2 T1290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr11:6643057 G>A maps to NM_003737.2 S3283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr11:6655408 C>A maps to NM_003737.2 R642R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr11:6648200 G>A maps to NM_003737.2 A2023A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr11:6651691 G>A maps to NM_003737.2 L1445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:6648422 C>T maps to NM_003737.2 T1949T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:6651836 G>A maps to NM_003737.2 F1396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr11:6662559 G>A maps to NM_003737.2 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:6648746 C>T maps to NM_003737.2 L1841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:155305518 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:155157961 G>T maps to NM_017639.3 V2159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:155180750 G>A maps to NM_017639.3 S1790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr4:155312368 A>G maps to NM_017639.3 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:155155990 C>T maps to NM_017639.3 K2816K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:155157010 G>A maps to NM_017639.3 T2476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr4:155176717 C>T maps to NM_017639.3 V1843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr4:155254200 G>T maps to NM_017639.3 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr4:155254512 C>T maps to NM_017639.3 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr4:155237083 C>T maps to NM_017639.3 L1237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr4:155241753 C>T maps to NM_017639.3 R1144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:155156344 C>G maps to NM_017639.3 V2698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr4:155191120 G>A maps to NM_017639.3 Q1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr4:155219684 A>G maps to NM_017639.3 N1472N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr4:155249331 G>A maps to NM_017639.3 Q856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr4:155191120 G>A maps to NM_017639.3 Q1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr16:2296928 C>T maps to NM_001919.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:71892390 C>T maps to ENST00000504952 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr4:71891531 G>C did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr4:71888181 C>T maps to ENST00000504952 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr13:36383153 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:36445358 A>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr13:36410270 C>T maps to NM_004734.4 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr4:151170829 C>T maps to NM_001040261.4 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr4:151142827 G>T did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr4:151153946 C>T maps to NM_001040261.4 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr3:36779214 A>T maps to NM_033403.1 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr10:115607067 G>A maps to NM_014881.3 Q718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr10:115609944 C>A maps to NM_014881.3 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr10:115596919 G>A maps to NM_014881.3 Q955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr10:115610375 G>C maps to NM_014881.3 S163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:114454729 C>T maps to NM_022836.3 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr10:14995988 C>T maps to NM_001033855.1 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr3:53346345 C>T maps to ENST00000480258 Q145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:53326413 C>T maps to ENST00000480258 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr3:53338235 C>A maps to ENST00000480258 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:2058389 G>A maps to NM_152640.3 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr12:2061974 G>C maps to NM_152640.3 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr5:112336848 C>T maps to NM_152624.4 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr11:126201376 C>T maps to NM_014026.3 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr11:126176556 G>A maps to NM_014026.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr1:155006974 G>A maps to NM_152494.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr1:155013943 G>A maps to NM_152494.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr1:155015922 G>A maps to NM_152494.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr1:155018443 G>A maps to NM_152494.3 Q416Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:155018906 C>T maps to NM_152494.3 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:155020371 C>G maps to NM_152494.3 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:155013955 G>T maps to NM_152494.3 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr1:155001748 G>A maps to NM_144622.2 D434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr1:155001802 G>A maps to NM_144622.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:155001831 G>A maps to NM_144622.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:155003041 G>C maps to NM_144622.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:155004161 A>G maps to NM_144622.2 C209C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr13:95114289 G>A maps to NM_001129889.1 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr13:95131236 G>A maps to NM_001129889.1 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr13:95114444 T>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr4:183814212 G>C maps to NM_001012732.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:74600063 C>T maps to NM_004082.4 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr2:74594523 G>T maps to NM_004082.4 A736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:34616066 C>T maps to NM_007234.3 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:150110696 C>T maps to NM_001135643.1 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr5:150095148 G>A maps to NM_001135643.1 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr16:23678371 C>G maps to NM_032486.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr8:30038094 G>A maps to NM_006571.2 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr8:30021635 T>A maps to NM_006571.2 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr3:182681825 C>A maps to NM_020640.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr13:114138203 C>T maps to NM_001014283.1 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr16:20871408 G>A maps to NM_173475.2 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr16:20871596 C>A maps to NM_173475.2 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr16:20871597 T>C maps to NM_173475.2 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr4:52752756 G>T maps to ENST00000451288 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:102937214 G>A maps to NM_032299.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr23:110654177 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:110653274 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:110576299 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr23:110555911 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr19:17426804 G>T did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:85787135 C>G maps to NM_012137.3 *286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr6:31696057 G>A maps to NM_013974.1 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr6:31696842 G>A maps to NM_013974.1 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:31695034 G>A maps to NM_013974.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr11:61081798 G>A maps to NM_001923.3 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr11:61071441 G>A maps to NM_001923.3 I909I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr11:61083865 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr11:61076541 T>C maps to NM_001923.3 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr11:47260363 C>T maps to NM_000107.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr11:47254497 C>G maps to NM_000107.2 S197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr11:47256450 C>T maps to NM_000107.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:47259518 G>A maps to NM_000107.2 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr11:47256390 C>G maps to NM_000107.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BS-01A-21D-A26M-08 chr11:47256318 C>T maps to NM_000107.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:47254408 C>T maps to NM_000107.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr11:47236797 C>G maps to NM_000107.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:47259413 C>T maps to NM_000107.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:47259488 C>T maps to NM_000107.2 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:50571757 C>G did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:103908029 C>G maps to NM_001001711.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:103907711 C>T maps to NM_001001711.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:15956938 C>T maps to NM_032341.4 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:15959932 G>C did not map to a codon.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr10:74034624 G>A maps to NM_019058.2 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr4:101109324 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:49391910 G>A maps to NM_015086.1 Q250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:49392961 C>A maps to NM_015086.1 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr12:49392971 T>C maps to NM_015086.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:110726085 G>A maps to NM_003649.2 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr6:110729592 G>C maps to NM_003649.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr6:30865194 C>G maps to NM_013994.2 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:162745931 C>G maps to NM_006182.2 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr20:3183979 C>T maps to NM_023935.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:3180685 C>T maps to NM_023935.1 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:15746296 C>T maps to NM_004939.1 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr2:15768963 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:108547944 C>A maps to NM_004398.2 S171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr11:108547867 C>T maps to NM_004398.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:31255896 C>T maps to NM_030653.3 F800F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr12:31246217 G>A maps to NM_030653.3 Q443Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:31237974 G>T maps to NM_030653.3 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr12:31236982 G>A maps to NM_030653.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr22:38891016 C>G maps to NM_001098504.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr22:38902218 C>A maps to NM_001098504.1 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:118582551 C>T maps to NM_006773.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:70363868 C>T maps to NM_007242.4 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:70367483 G>A maps to NM_007242.4 *480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr16:70358512 C>T maps to NM_007242.4 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr16:70349881 T>G maps to NM_007242.4 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:112299298 G>A maps to NM_007204.4 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr1:112309337 G>A maps to NM_007204.4 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr1:112308377 G>C maps to NM_007204.4 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:112309337 G>C maps to NM_007204.4 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr1:112303846 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:112303150 C>T maps to NM_007204.4 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:112309356 C>T maps to NM_007204.4 Q771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:70719869 G>A maps to NM_004728.2 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr10:70721908 C>T maps to NM_004728.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr10:70719908 G>A maps to NM_004728.2 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:49230567 G>A maps to NM_004818.2 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:49231128 G>A maps to NM_004818.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:49226344 G>A maps to NM_004818.2 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr12:49230395 G>A maps to NM_004818.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr12:49224475 C>G did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr14:94517752 C>T maps to NM_020414.3 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr14:94517584 C>T maps to NM_020414.3 P844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr14:94545644 G>A maps to NM_020414.3 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr23:134709104 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:134679383 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:134680740 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr23:134680352 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:134709060 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SU-01A-31D-A391-08 chr23:134654979 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr23:134706852 A>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:134681099 C>A did not map to a codon.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr23:134683628 C>G did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr20:47841696 C>T maps to NM_017895.7 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr20:47839803 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr16:68057078 G>A maps to NM_018380.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr19:14521879 G>A maps to ENST00000451994 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:14520162 G>A maps to ENST00000451994 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr23:41204467 A>T did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:41202026 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:41203032 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr23:41203611 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr23:41206589 G>T did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:41203071 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr23:41206265 G>T did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr23:41206689 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:41204655 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:41206928 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr23:41204701 G>T did not map to a codon.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr23:41201839 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr23:41204494 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:41196682 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr23:41205789 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr24:15025699 C>A did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr5:55094376 C>G maps to NM_024415.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr5:55077778 C>T maps to NM_024415.2 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr5:55075821 C>G maps to NM_024415.2 S142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr5:176939802 G>A maps to NM_016222.2 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr5:176942242 C>T maps to NM_016222.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr5:176939620 G>A maps to NM_016222.2 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:61888506 C>T maps to NM_203499.1 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr17:61869906 C>T maps to NM_203499.1 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:74117796 C>T maps to NM_018665.2 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:74125922 C>T maps to NM_018665.2 Q641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:74119056 G>A maps to NM_018665.2 Q422Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr5:134143531 A>C maps to ENST00000452510 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr12:12980269 G>C maps to NM_016355.3 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:19033502 C>T maps to NM_019070.4 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr19:19033466 C>T maps to NM_019070.4 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:19032501 C>T maps to NM_019070.4 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr17:62496162 G>A maps to NM_004396.3 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:62499952 G>A maps to NM_004396.3 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:62496181 C>T maps to NM_004396.3 Q568Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr10:70706347 C>T maps to NM_024045.1 R726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:132624719 C>T maps to NM_175066.3 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr12:132624236 C>T maps to NM_175066.3 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr12:132625035 G>A maps to NM_175066.3 F535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:35990092 C>G maps to NM_007010.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr17:35988701 T>C maps to NM_007010.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr23:23019297 T>C did not map to a codon.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr23:23019071 C>A did not map to a codon.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr23:23019218 A>T did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr23:23019521 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr23:23019977 G>A did not map to a codon.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr12:113600768 C>T maps to NM_001111322.1 Q721Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr12:124104078 C>T maps to NM_020936.1 D478D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr12:124094536 C>T maps to NM_020936.1 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr9:32457120 C>G maps to NM_014314.3 *926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:200633162 G>A maps to NM_001031725.4 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr4:169204636 G>C maps to NM_017631.5 S561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr4:169196558 C>T maps to NM_017631.5 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr4:169167597 C>A maps to NM_017631.5 G1379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:169196501 T>C maps to NM_017631.5 T766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:169223567 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr4:169157520 G>C maps to NM_017631.5 S1472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr4:169229286 G>C maps to NM_017631.5 S45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr4:169374373 G>A maps to NM_001012967.1 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr4:169382906 G>A maps to NM_001012967.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr4:169336859 G>A maps to NM_001012967.1 L939L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr11:688403 C>G maps to NM_021008.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr9:118163569 C>G maps to NM_017418.2 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:91055004 C>T maps to NM_001359.1 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr8:91054994 C>T maps to NM_001359.1 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr8:91013776 C>T maps to NM_001359.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr8:91013750 C>T maps to NM_001359.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr8:91013776 C>T maps to NM_001359.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr8:91013743 C>T maps to NM_001359.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr8:91064100 C>G maps to NM_001359.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:161094072 G>A maps to ENST00000368005 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr16:90015977 C>T maps to NM_207514.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr16:90028178 C>T maps to NM_207514.1 Y299Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr16:90016034 G>A maps to NM_207514.1 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr16:90015914 G>A maps to NM_207514.1 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:6914117 C>T maps to NM_021010.1 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr8:6912953 C>T maps to NM_021010.1 *95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr8:6782354 T>C maps to NM_001926.3 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr6:49986802 A>G maps to NM_001037497.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr6:50011359 C>T maps to NM_001037498.1 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr6:49936458 G>A maps to NM_001037729.1 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr20:29965111 G>A maps to NM_153289.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:30037946 C>A maps to NM_153324.2 Y58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr20:30053433 G>A maps to NM_001037500.1 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr20:76883 G>C maps to NM_153325.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr20:126331 G>A maps to NM_030931.2 *112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:139535 C>T maps to NM_139074.2 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr20:139610 A>G maps to NM_139074.2 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr20:168639 C>A maps to NM_001037732.1 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr4:9452167 T>C maps to NM_001040448.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr14:100615442 G>A maps to NM_206918.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr14:100615442 G>A maps to NM_206918.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr1:40980427 C>A maps to NM_022774.1 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:40981298 C>G maps to NM_022774.1 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr9:126144640 G>A maps to NM_020946.1 P700P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr9:126220080 G>A maps to NM_020946.1 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr9:126143803 C>T maps to NM_020946.1 Q979Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr9:126144826 G>C maps to NM_020946.1 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:197641246 T>G maps to NM_001195215.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:6467704 G>C maps to NM_024898.2 S739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:6479702 G>A maps to NM_024898.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr19:6468319 C>T maps to NM_024898.2 K572K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr7:140301915 C>T maps to NM_015689.3 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:140301336 G>A maps to NM_015689.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr7:140255468 C>G maps to NM_015689.3 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr7:140301531 C>T maps to NM_015689.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr7:140227216 C>A maps to NM_015689.3 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr7:140258000 G>C maps to NM_015689.3 S634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr7:140244440 G>A maps to NM_015689.3 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr1:115147541 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:115147613 C>T maps to ENST00000393274 E532E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:115168461 C>G maps to ENST00000393274 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr1:115137118 C>T maps to ENST00000393274 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:111734818 G>A maps to NM_024901.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr8:142178484 G>A maps to NM_014957.2 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr8:142202476 C>T maps to NM_014957.2 Q1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr8:142161800 C>T maps to NM_014957.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr8:142176342 C>T maps to NM_014957.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr15:66048723 G>C maps to ENST00000443035 S22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr15:65983667 G>A maps to ENST00000443035 L1088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr15:66015200 G>A maps to ENST00000443035 Q525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr15:66044728 G>C maps to ENST00000443035 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr1:153912911 G>C maps to NM_014856.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr1:153912941 G>A maps to NM_014856.2 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:153906267 C>G maps to NM_014856.2 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:153916544 G>A maps to NM_014856.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr1:153905782 G>A maps to NM_014856.2 L1115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr1:153915440 G>A maps to NM_014856.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr1:153905129 G>A maps to NM_014856.2 N1249N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:153905711 G>A maps to NM_014856.2 L1138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr9:19316745 T>A maps to NM_017925.4 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr9:19346900 G>A maps to NM_017925.4 L1093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:9161319 G>A maps to NM_015213.2 I1254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr11:9199866 G>C maps to NM_015213.2 S573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr11:9191465 C>T maps to NM_015213.2 W696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:9167351 G>A maps to NM_015213.2 Y956Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr11:9167360 C>T maps to NM_015213.2 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr11:9225495 C>T maps to NM_015213.2 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr11:9167251 G>A maps to NM_015213.2 Q990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:31632936 C>A maps to NM_144973.3 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:31613258 G>A maps to NM_144973.3 Q321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr12:31604939 G>A maps to NM_144973.3 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr12:31586145 C>T maps to NM_144973.3 R683R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:31613132 G>A maps to NM_144973.3 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr12:31613288 C>A maps to NM_144973.3 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:123253410 C>T maps to ENST00000455982 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr1:68954597 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr5:59893729 G>A maps to NM_018369.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr5:59982970 G>A maps to NM_018369.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr12:100657357 G>C maps to ENST00000422147 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr12:100657669 T>C maps to ENST00000422147 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr22:32275582 G>A maps to NM_001136029.1 W1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr22:32160959 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr22:32188757 C>G maps to NM_001136029.1 S241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr22:32242866 G>A maps to NM_001136029.1 T1014T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:32188757 C>G maps to NM_001136029.1 S241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr22:32217539 G>A maps to NM_001136029.1 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr8:120977540 C>T maps to NM_022783.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr8:120886109 C>T maps to NM_022783.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr8:121013839 G>T maps to NM_022783.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr8:121013827 G>A maps to NM_022783.2 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr11:33053079 G>A maps to NM_001077242.1 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr12:16189257 G>A maps to NM_015954.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:16109915 G>A maps to NM_015954.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr12:16189269 C>G maps to NM_015954.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr17:5383884 C>T maps to NM_016041.3 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr22:24179996 G>A maps to NM_001135751.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr2:220285560 G>A maps to NM_001927.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:10532398 G>C maps to NM_004401.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:10532451 G>A maps to NM_004401.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:3800259 C>T maps to ENST00000430539 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:24749945 G>C maps to NM_001127453.1 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr7:24784230 C>T maps to NM_001127453.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr7:24745980 G>T maps to NM_001127453.1 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:24756951 G>A maps to NM_001127453.1 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr7:24789222 G>A maps to NM_001127453.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr7:24745821 G>A maps to NM_001127453.1 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr9:117266849 G>A maps to NM_015404.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr9:117185764 C>T maps to NM_015404.3 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:179320860 C>T maps to NM_001042702.3 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr2:179319143 C>T maps to NM_001042702.3 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr2:179323265 G>A maps to NM_001042702.3 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr8:145542171 G>A maps to NM_012079.4 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr8:145542409 G>C maps to NM_012079.4 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr11:75509418 C>G maps to NM_032564.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:69419712 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr23:69421859 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr23:69421864 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr23:69424218 G>C did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:69424938 G>C did not map to a codon.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr22:18897773 C>T maps to NM_005675.4 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr22:20073686 C>T maps to NM_022720.6 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr22:20073752 G>A maps to NM_022720.6 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr12:56335034 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:56334171 C>T maps to NM_201554.1 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:56345847 C>T maps to NM_201554.1 I539I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr12:56334763 G>A maps to NM_201554.1 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:56336045 A>G maps to NM_201554.1 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr12:56334709 A>G maps to NM_201554.1 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr7:14733764 G>A maps to NM_004080.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr7:14217702 C>T maps to NM_004080.2 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr7:14758227 C>T maps to NM_004080.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr7:14724924 G>A maps to NM_004080.2 C258C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:234359571 G>A maps to NM_152879.2 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:234357966 G>A maps to NM_152879.2 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr17:54912383 G>A maps to NM_003647.2 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr3:186015940 G>A maps to NM_001346.2 H74H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr3:186006619 C>T maps to NM_001346.2 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:185905997 G>A maps to NM_001346.2 C696C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:186038186 G>C maps to NM_001346.2 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:185997707 G>A maps to NM_001346.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:185906060 C>T maps to NM_001346.2 K675K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:42763215 G>A maps to NM_178009.2 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr13:42734246 G>A maps to NM_178009.2 W277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr13:42793923 C>T maps to NM_178009.2 Q1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr13:42764539 T>G maps to NM_178009.2 V638V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr13:42740772 C>T maps to NM_178009.2 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:137341244 G>A maps to NM_004717.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr7:137363350 C>A maps to NM_004717.2 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr7:137080373 T>A maps to NM_004717.2 A1017A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr23:50213367 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr23:50129551 C>G did not map to a codon.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr23:50163447 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr23:50121634 C>A did not map to a codon.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr23:50213511 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:50129584 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr23:50111994 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr23:50213549 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:50146090 G>C did not map to a codon.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr23:50117980 C>T did not map to a codon.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr23:50130616 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:50123016 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:50125512 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:50213561 G>A did not map to a codon.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr4:961426 C>T maps to NM_001347.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr4:954953 C>T maps to NM_001347.2 R870R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:46394036 G>A maps to NM_001105540.1 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:46398101 C>T maps to NM_001105540.1 I918I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr11:46400545 G>A maps to NM_001105540.1 Q996Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:46397142 G>A maps to NM_001105540.1 Q812Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr11:46400034 G>A maps to NM_001105540.1 R989R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr11:46397157 G>A maps to NM_001105540.1 R817R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr1:55331116 C>T maps to NM_014762.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:71152463 G>A maps to NM_001360.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:26772805 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:49437013 C>T maps to NM_014475.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr10:99358535 C>T maps to NM_138413.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr5:79945221 G>A maps to NM_000791.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:49485100 C>T maps to NM_021044.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:49488196 G>A maps to NM_021044.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:49484980 G>T maps to NM_021044.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr16:72057472 C>T maps to NM_001361.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr16:72058042 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr19:12792436 G>A maps to NM_001930.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr19:12786938 G>A maps to NM_001930.2 Y302Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr19:12792433 G>A maps to NM_001930.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr19:12792433 G>A maps to NM_001930.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:24768167 G>A maps to NM_001136050.2 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr14:24766075 G>A maps to NM_001136050.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr14:24760828 G>A maps to NM_001136050.2 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:34956405 C>T maps to NM_024308.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr17:34951593 G>A maps to NM_024308.3 W114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:27228277 G>A maps to NM_144683.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr14:24109079 G>A maps to NM_182908.4 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:12639356 G>C maps to NM_004753.4 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:12640691 A>G maps to NM_004753.4 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:12640574 C>T maps to NM_004753.4 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:24424330 G>A maps to NM_021004.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr14:24507005 C>T maps to NM_001082488.1 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr14:24518020 G>C did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr14:24506960 C>T maps to NM_001082488.1 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr14:24505783 C>T maps to NM_001082488.1 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr14:24459504 G>A maps to NM_198083.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr14:60619881 G>A maps to NM_016029.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr17:21087049 C>A maps to NM_015510.3 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr17:9683241 A>G maps to ENST00000330255 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:169939947 C>T maps to NM_001142271.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:169939918 G>T maps to NM_001142271.1 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:169939947 C>T maps to NM_001142271.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:2343323 C>T did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr23:2209620 C>T did not map to a codon.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr23:2184835 C>T did not map to a codon.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr23:2343294 C>A did not map to a codon.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr23:2209582 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr10:12155059 C>T maps to NM_018706.5 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr10:12139832 G>A maps to NM_018706.5 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:12142257 C>T maps to NM_018706.5 Q585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:24550639 A>G maps to NM_001358.2 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr4:24558033 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr4:24550570 G>A maps to NM_001358.2 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr4:24544625 T>C maps to NM_001358.2 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr4:24578091 G>C maps to NM_001358.2 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr4:24572370 G>A maps to NM_001358.2 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:30638683 C>T maps to NM_003587.4 W164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr6:30632640 G>C maps to NM_003587.4 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr5:54581185 C>A maps to NM_019030.2 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr5:54581606 C>G maps to NM_019030.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr5:54555736 C>T maps to NM_019030.2 L1332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:47868906 C>T maps to NM_138615.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr3:47887800 C>A maps to NM_138615.2 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr3:47890699 C>G maps to NM_138615.2 S983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr3:47887267 G>T maps to NM_138615.2 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr3:47868906 C>T maps to NM_138615.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr3:47887806 G>A maps to NM_138615.2 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:127527688 G>A maps to NM_018180.2 R588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:5365686 C>T maps to ENST00000457531 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:5371894 G>A maps to ENST00000457531 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:5347828 G>C maps to ENST00000457531 S666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:5372146 C>T maps to ENST00000457531 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr17:5352146 C>G maps to ENST00000457531 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr19:47858558 C>T maps to NM_014681.5 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:47879303 C>T maps to NM_014681.5 Q811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr19:47856508 G>A maps to NM_014681.5 K74K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:37621004 C>T maps to NM_021931.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr20:37639028 C>G maps to NM_021931.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr3:154042034 C>T maps to NM_020865.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:125451374 C>T maps to NM_032656.3 K518K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:125470710 C>T maps to NM_032656.3 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr12:125461915 G>A maps to NM_032656.3 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr12:125449082 G>A maps to NM_032656.3 Y634Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr12:125449487 C>T maps to NM_032656.3 E600E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr12:125473493 G>A maps to NM_032656.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:125467118 C>T maps to NM_032656.3 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr16:72130343 C>T maps to NM_014003.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:72139992 G>A maps to NM_014003.3 R859R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:39042770 G>A maps to NM_198963.1 F1166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr2:39041019 C>T maps to NM_198963.1 E1208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:40260105 C>T maps to NM_024119.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr17:40255714 G>C maps to NM_024119.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr17:40256927 C>G maps to NM_024119.2 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr17:41585852 C>T maps to NM_004941.1 R823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr17:41585253 C>T maps to NM_004941.1 F729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr17:41585878 C>A maps to NM_004941.1 G831G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:182823163 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr1:182841624 C>T maps to NM_001357.4 Q571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:182856268 C>T maps to NM_001357.4 S1171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr1:182850747 C>G maps to NM_001357.4 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr1:182852702 C>T maps to NM_001357.4 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr12:122702860 G>C maps to NM_019887.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr12:122710528 G>A maps to NM_019887.4 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:140958171 G>A maps to ENST00000398557 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr23:96220142 G>A did not map to a codon.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr23:96354742 G>C did not map to a codon.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr23:96167541 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr23:96136710 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr23:96185756 C>A did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr23:96192268 A>T did not map to a codon.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr23:96213048 C>T did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr23:96854278 C>G did not map to a codon.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr23:96396758 T>C did not map to a codon.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr23:96171542 C>T did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:96192267 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:96171542 C>A did not map to a codon.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr23:95993757 G>C did not map to a codon.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr23:96213048 C>T did not map to a codon.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr23:96854269 T>C did not map to a codon.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr23:96684677 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAME-01A-12D-A42E-08 chr23:96171554 T>G did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:96203942 G>T did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:96369881 T>G did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr23:95993699 A>G did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr23:95993711 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr23:96171542 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr13:60348371 C>T maps to NM_001042517.1 Q1090Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr13:60407255 G>A maps to NM_001042517.1 F1004F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:95592922 C>T maps to NM_177438.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr14:95562264 C>T maps to NM_177438.2 S1664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr14:95556945 T>A maps to NM_177438.2 G1886G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr14:95569760 C>T maps to NM_177438.2 K1324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr14:95562204 G>A maps to NM_177438.2 L1684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr14:95560458 C>A maps to NM_177438.2 A1710A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr14:95579562 T>A did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr14:95562507 G>A maps to NM_177438.2 L1583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr14:95560416 C>T maps to NM_177438.2 P1724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr20:61526263 C>T maps to NM_033081.2 V778V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr20:61525840 G>A maps to NM_033081.2 V832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr20:61526406 C>T maps to NM_033081.2 A775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr20:61526466 C>G maps to NM_033081.2 V755V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr20:61522432 G>A maps to NM_033081.2 F1140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr20:61537308 C>A maps to NM_033081.2 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr20:61511414 G>A maps to NM_033081.2 Q1965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr20:61512977 G>A maps to NM_033081.2 L1444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr20:61512798 C>T maps to NM_033081.2 Q1503Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr20:61528238 G>A maps to NM_033081.2 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr20:61525864 C>T maps to NM_033081.2 K824K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr20:61510941 G>A maps to NM_033081.2 N2122N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr20:61512240 C>T maps to NM_033081.2 A1689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr20:61513001 C>A maps to NM_033081.2 E1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr20:61510986 G>A maps to NM_033081.2 G2107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr20:61512312 G>A maps to NM_033081.2 C1665C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr5:61688039 G>C maps to NM_014473.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr5:61688796 C>T maps to NM_014473.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr1:54371912 C>T maps to NM_000792.5 Y209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:54359912 G>A maps to NM_000792.5 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr14:80677626 G>A maps to NM_001007023.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr14:80677656 G>A maps to NM_001007023.2 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr21:47985663 C>T maps to ENST00000318711 Y1402Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr21:47953950 G>A maps to ENST00000318711 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr21:47931384 G>A maps to ENST00000318711 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr21:47969716 C>T maps to ENST00000318711 D853D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr21:47976000 G>T maps to ENST00000318711 V1166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:51138368 G>T did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:51065078 C>T maps to NM_173602.2 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr12:51090910 C>A maps to NM_173602.2 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr12:51092152 C>G maps to NM_173602.2 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr12:51118559 C>T maps to NM_173602.2 V1097V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr12:51086795 G>A maps to NM_173602.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr10:486826 G>A maps to NM_014974.2 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr10:375375 G>C maps to NM_014974.2 L1250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr10:454928 G>C maps to NM_014974.2 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr10:332257 G>T maps to NM_014974.2 A1358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr10:468821 C>T maps to NM_014974.2 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr19:2717723 G>A maps to NM_145173.3 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:68512368 G>A maps to NM_004675.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr1:68512938 C>A maps to NM_004675.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:68512851 G>T maps to NM_004675.2 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr3:122598122 C>T maps to NM_032839.2 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr3:122552162 G>C did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr13:73334744 A>G maps to NM_014953.3 D905D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr13:73347944 G>C maps to NM_014953.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr13:73343020 C>T maps to NM_014953.3 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr15:66587329 G>A maps to NM_001143688.1 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr15:66621340 T>C maps to NM_001143688.1 N745N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:231830214 C>T maps to NM_001164537.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr1:232144701 C>T maps to NM_001164537.1 S770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr1:223178659 G>A maps to NM_032890.2 Q1307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:223178773 C>A maps to NM_032890.2 A1345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:223175803 A>G maps to NM_032890.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr1:223177435 G>A maps to NM_032890.2 R899R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:223116203 G>A maps to NM_032890.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr15:40660106 C>T maps to NM_033510.1 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr15:40661478 C>T maps to NM_033510.1 L1056L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr15:40660724 C>T maps to NM_033510.1 S804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr15:40659809 C>T maps to NM_033510.1 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr11:111848508 C>T maps to NM_033425.3 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:111888512 G>A maps to NM_001037954.2 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:111853157 G>A maps to NM_001037954.2 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr11:111853165 A>G maps to NM_001037954.2 *291W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr23:153993190 A>T did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:153995276 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr11:65547231 T>A maps to NM_138368.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr11:65547168 C>T maps to NM_138368.3 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:65547045 T>C maps to NM_138368.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:65545713 G>T maps to NM_138368.3 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47S-01A-11D-A23U-08 chr10:54074409 T>C maps to NM_012242.2 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:54076459 G>T maps to NM_012242.2 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr10:54074418 G>A maps to NM_012242.2 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr4:107956671 G>C maps to NM_014421.2 S26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr4:107846959 A>G maps to NM_014421.2 N123N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr4:107845254 T>C maps to NM_014421.2 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr11:11986169 G>A maps to ENST00000450094 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:11987390 G>T maps to ENST00000450094 C265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr11:12023936 C>T maps to ENST00000450094 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr8:42234536 C>T maps to NM_014420.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:49867962 C>G maps to NM_014419.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:111922052 G>A maps to NM_001931.4 W498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr8:12958063 G>A maps to NM_182643.2 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:12947970 C>T maps to NM_182643.2 E1288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:13357442 T>C maps to NM_182643.2 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr8:12958111 G>A maps to NM_182643.2 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr8:12956998 C>T maps to NM_182643.2 Q949Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr8:13259008 G>A maps to NM_182643.2 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr8:12950221 T>C maps to NM_182643.2 A1213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr8:12958129 C>T maps to NM_182643.2 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr8:12947859 G>A maps to NM_182643.2 L1325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr7:107531735 T>A did not map to a codon.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr7:107542258 C>T maps to NM_000108.3 F65F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-4Z-AA7W-01A-11D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr3:38138128 G>A maps to NM_007335.2 V747V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr3:38134327 C>T maps to NM_007335.2 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr3:38163976 C>T maps to NM_007337.2 Q1740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr3:38135240 G>C maps to NM_007335.2 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr3:38163812 G>A maps to NM_007335.2 V1726V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr3:38087161 G>A maps to NM_007335.2 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr13:51417482 C>T maps to ENST00000504404 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7N-01A-11D-A391-08 chr3:196867114 G>A maps to NM_004087.2 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr3:197023308 G>C maps to NM_004087.2 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr3:197024063 C>T maps to NM_004087.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:196921430 A>T maps to NM_004087.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:83195223 G>A maps to NM_001142699.1 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr11:83673941 G>A maps to NM_001142699.1 D442D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr11:83641424 G>C maps to NM_001142699.1 S481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:83810075 C>T maps to NM_001142699.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr11:83810000 T>A maps to NM_001142699.1 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr11:83344294 G>A maps to NM_001142699.1 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:69719848 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:69672535 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr23:69672524 C>T did not map to a codon.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr23:69672575 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr23:69670625 C>T did not map to a codon.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr23:69715264 C>A did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr23:69672518 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr23:69712061 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr23:69699074 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:69673485 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:69719872 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:7121569 G>C maps to NM_001365.3 S50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:7096311 G>A maps to NM_001365.3 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr17:7094101 G>T maps to NM_001365.3 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr17:7107012 G>A maps to NM_001365.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr10:79567621 C>G maps to NM_004747.3 L1576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr10:79576343 G>T maps to NM_004747.3 V1330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:79686096 A>T maps to NM_004747.3 L61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr10:79595677 G>A maps to NM_004747.3 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr10:79601695 G>C maps to NM_004747.3 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr10:79565544 G>T maps to NM_004747.3 S1681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:79571743 G>T maps to NM_004747.3 T1420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr10:79566550 C>T maps to NM_004747.3 Q1644Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr10:79614021 T>G maps to NM_004747.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr10:79570916 G>A maps to NM_004747.3 V1466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr10:79581140 G>C maps to NM_004747.3 S1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr10:79584174 G>A maps to NM_004747.3 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr10:79572014 G>A maps to NM_004747.3 I1382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr18:3508615 G>C maps to NM_004746.2 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr18:3499317 C>T maps to NM_004746.2 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr18:3879140 G>A maps to NM_004746.2 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr18:3879116 G>A maps to NM_004746.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr18:3499314 C>T maps to NM_004746.2 E934E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr18:3879167 G>A maps to NM_004746.2 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr8:1645431 C>T maps to ENST00000357934 N914N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr8:1626565 G>T maps to ENST00000357934 G767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr8:1626492 C>A maps to ENST00000357934 S743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr8:1649570 G>A maps to ENST00000357934 *998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr8:1616627 G>A maps to ENST00000357934 Q590Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:35370069 C>G maps to NM_001080418.1 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:35365868 C>T maps to NM_001080418.1 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr20:35128658 G>A maps to ENST00000339266 Q719Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr20:35064674 C>A maps to ENST00000339266 S388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr20:35064618 C>T maps to ENST00000339266 Y369Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr20:35060911 G>A maps to ENST00000339266 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr14:55625315 C>A maps to NM_014750.4 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr14:55618518 C>G maps to NM_014750.4 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr14:101201202 C>T maps to NM_003836.5 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr6:170594689 G>A maps to NM_005618.3 Q277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:170592470 G>A maps to NM_005618.3 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr6:170592090 G>A maps to NM_005618.3 C717C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr15:41228777 C>T maps to NM_019074.3 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr15:41222830 C>T maps to NM_019074.3 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:41226821 C>T maps to NM_019074.3 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr15:41222181 C>T maps to NM_019074.3 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr15:41222205 C>T maps to NM_019074.3 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr15:41222304 C>T maps to NM_019074.3 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr14:75369020 C>G maps to NM_001933.4 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr14:75365128 C>G maps to NM_001933.4 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr2:172951430 C>T maps to NM_178120.4 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr17:48068881 C>T maps to NM_005220.2 *288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:48072149 G>C maps to NM_005220.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:48046846 C>T maps to NM_138281.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr7:96650244 C>A maps to NM_005221.5 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr10:124385473 C>A maps to ENST00000368915 T1887T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr10:124390510 C>A maps to ENST00000368915 S2020S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:124358520 C>G maps to ENST00000368915 S1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr10:124331830 T>C maps to ENST00000368915 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr10:124339406 C>T maps to ENST00000368915 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr10:124402856 C>T maps to ENST00000368915 V2524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr10:124357508 C>G maps to ENST00000368915 T979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr10:124348478 C>T maps to ENST00000368915 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr10:124377582 C>T maps to ENST00000368915 R1648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr10:124399734 C>T maps to ENST00000368915 V2374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr10:124399767 C>T maps to ENST00000368915 N2385N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr10:124336079 C>G maps to ENST00000368915 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr10:124392386 C>T maps to ENST00000368915 L2126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr1:46976635 C>T maps to NM_147192.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr1:46976773 C>A maps to NM_147192.2 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMW-01A-11D-A42E-08 chr1:46976758 C>T maps to NM_147192.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr23:32717354 G>C did not map to a codon.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr23:32716115 C>T did not map to a codon.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr23:31950194 A>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr23:31986489 C>G did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:32591713 A>T did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:32429879 G>A did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:31947823 G>C did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr23:31645810 T>G did not map to a codon.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr23:32662324 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr23:32235110 T>C did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr23:32383165 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr23:31227733 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:31838187 C>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:32583870 A>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:32663159 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr23:32360314 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr23:31525405 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr23:32361348 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr23:32328366 C>A did not map to a codon.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr23:31497126 G>C did not map to a codon.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr23:32466659 T>G did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:32398670 C>G did not map to a codon.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr23:32407732 T>G did not map to a codon.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr23:31676242 G>A did not map to a codon.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr23:32305646 C>T did not map to a codon.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr23:32591917 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr23:32361362 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr23:32591736 C>T did not map to a codon.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr23:32398641 T>G did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:31165507 C>G did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:32536201 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr23:32382782 G>T did not map to a codon.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr23:32235147 C>T did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:32328261 G>C did not map to a codon.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr23:32503196 G>T did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr23:31140028 A>G did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr23:32429984 G>T did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr23:32503147 C>T did not map to a codon.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr23:32486810 A>G did not map to a codon.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr23:32466741 T>G did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr23:32360260 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr23:32827619 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr23:32503182 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:32490312 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr23:31838152 T>A did not map to a codon.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr23:31792254 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr23:32717338 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr23:32328203 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr23:32408214 T>A did not map to a codon.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr5:78326676 G>C maps to NM_013391.2 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:78322342 G>A maps to NM_013391.2 I698I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr5:78359610 C>G did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr5:78347188 C>T maps to NM_013391.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:35993779 G>A maps to NM_033317.4 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr4:88577664 C>T maps to NM_004407.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:46282708 C>T maps to NM_004409.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr9:916854 C>A maps to NM_021951.2 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr9:968120 C>T maps to NM_021951.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr9:1057267 C>T maps to NM_181872.4 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr9:1056847 C>T maps to NM_181872.4 Q421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr9:990716 G>A maps to NM_021240.2 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr9:22451127 C>T maps to NM_022160.2 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:50884474 G>A maps to NM_032110.1 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr1:50884576 G>A maps to NM_032110.1 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:53930395 G>A maps to NM_033067.1 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr1:53927224 G>A maps to NM_033067.1 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:42351818 C>T maps to ENST00000427618 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:86794343 C>A maps to NM_021145.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr7:86808949 G>C maps to NM_021145.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr7:86817603 G>A maps to NM_021145.3 Q466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr7:86813795 C>T maps to NM_021145.3 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr19:46290006 C>T maps to NM_004943.1 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:46289403 G>C maps to NM_004943.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:46289784 C>T maps to NM_004943.1 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:118487670 C>T maps to NM_005509.4 R1548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr5:118505896 C>G maps to NM_005509.4 S1804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr5:118569087 C>T maps to NM_005509.4 Q2777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr5:118506140 C>T maps to NM_005509.4 I1885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr5:118469493 C>T maps to NM_005509.4 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr5:118506821 G>A maps to NM_005509.4 L2112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr5:118507479 C>G maps to NM_005509.4 S2166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr5:118539080 C>T maps to NM_005509.4 Q2605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr15:51834542 G>A maps to NM_001174116.1 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr15:51741240 C>A maps to NM_001174116.1 L3018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr15:51827925 C>G maps to NM_001174116.1 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr15:51780818 C>T maps to NM_001174116.1 R1659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr15:51772831 T>A maps to NM_001174116.1 V2157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr15:51772765 G>C maps to NM_001174116.1 L2179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr15:51755625 G>A maps to NM_001174116.1 Q2626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr15:51772974 G>A maps to NM_001174116.1 L2110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:51791784 A>G maps to NM_001174116.1 A1212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr10:70231668 G>T maps to NM_001080449.1 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr10:70206089 C>T maps to NM_001080449.1 Q426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr10:70204806 G>T maps to NM_001080449.1 S450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr3:52398862 C>G maps to ENST00000273600 L1782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr3:52404220 C>T maps to ENST00000273600 F2078F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:52394326 G>A maps to ENST00000273600 R1524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr3:52433024 C>G maps to ENST00000273600 L4147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:52356503 C>T maps to ENST00000273600 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr3:52382926 C>T maps to ENST00000273600 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr3:52398682 G>A maps to ENST00000273600 V1758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr3:52400858 G>T maps to ENST00000273600 T1907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:52383050 C>T maps to ENST00000273600 R752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr3:52387258 C>T maps to ENST00000273600 N1056N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr3:52361989 G>A maps to ENST00000273600 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr3:52432947 C>T maps to ENST00000273600 Q4122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr3:52391973 G>A maps to ENST00000273600 T1347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:52425568 G>T maps to ENST00000273600 T3398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:52429618 C>T maps to ENST00000273600 F3792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr12:124416628 C>A maps to NM_207437.3 R4306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr12:124345627 C>T maps to NM_207437.3 I2155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:124311274 G>A maps to NM_207437.3 L1289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:124326020 G>A maps to NM_207437.3 L1645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr12:124398989 C>T maps to NM_207437.3 D3371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr12:124362398 C>T maps to NM_207437.3 F2654F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:124415936 C>G maps to NM_207437.3 L4160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:124293451 C>T maps to NM_207437.3 I914I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:124298138 C>A maps to NM_207437.3 L1073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:124252151 G>T did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr12:124341733 C>T maps to NM_207437.3 D2072D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:124298404 C>G maps to NM_207437.3 L1124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr12:124345621 C>T maps to NM_207437.3 Y2153Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:124398923 G>A maps to NM_207437.3 L3349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr12:124401029 C>T maps to NM_207437.3 F3465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:124315200 C>A maps to NM_207437.3 L1382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr12:124359911 G>A maps to NM_207437.3 K2573K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:124403342 C>T maps to NM_207437.3 L3667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:124401032 C>T maps to NM_207437.3 L3466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr12:124352130 C>T maps to NM_207437.3 Q2311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr12:124352141 C>T maps to NM_207437.3 L2314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:124408908 C>A maps to NM_207437.3 S3781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr7:21621560 T>G maps to NM_003777.3 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr7:21658810 A>T maps to NM_003777.3 K1455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:21640355 G>A maps to NM_003777.3 V1021V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:21628897 T>C maps to NM_003777.3 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:21678628 C>T maps to NM_003777.3 F1635F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:21826372 C>G maps to NM_003777.3 V3250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr7:21747377 T>G maps to NM_003777.3 L2210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr7:21904151 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr7:21723452 G>T maps to NM_003777.3 E1845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr7:21939679 G>A maps to NM_003777.3 K4422K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr7:21628978 C>T maps to NM_003777.3 F709F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr7:21745075 A>T did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr7:21932041 G>C did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr7:21599257 G>T maps to NM_003777.3 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr7:21920408 G>A maps to NM_003777.3 L4102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr7:21784150 G>A maps to NM_003777.3 L2757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:21840769 C>T maps to NM_003777.3 L3355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:21826249 C>T maps to NM_003777.3 L3209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr7:21640364 C>T maps to NM_003777.3 I1024I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:21631026 C>T maps to NM_003777.3 N833N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr7:21939643 A>G maps to NM_003777.3 K4410K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:21737788 C>T maps to NM_003777.3 F2053F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr7:21723421 T>C maps to NM_003777.3 F1834F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr7:21788242 C>G maps to NM_003777.3 L2859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr7:21721172 C>T maps to NM_003777.3 L1785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:57496604 T>C maps to NM_178504.4 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:57487119 G>C maps to NM_178504.4 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:76503683 G>A maps to ENST00000389840 S1476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr17:76490165 G>A maps to ENST00000389840 V2106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FH-01A-11D-A38G-08 chr17:76454651 C>T maps to ENST00000389840 A3310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FM-01A-11D-A38G-08 chr17:76475639 C>T maps to ENST00000389840 T2595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr17:76497362 G>T maps to ENST00000389840 R1782R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:76490237 G>A maps to ENST00000389840 I2082I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:76557990 G>C maps to ENST00000389840 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:76487557 G>A maps to ENST00000389840 I2198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr17:76447592 G>A maps to ENST00000389840 A3550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr17:76567028 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:76533458 C>A maps to ENST00000389840 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr17:76433875 C>T maps to ENST00000389840 E3954E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr17:76562779 G>T maps to ENST00000389840 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:76451809 G>A maps to ENST00000389840 F3348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr17:76451911 G>T maps to ENST00000389840 V3314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr17:76521177 G>A maps to ENST00000389840 F1255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr17:76554222 G>A maps to ENST00000389840 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr17:76490791 C>G maps to ENST00000389840 L2037L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr17:76481698 C>G maps to ENST00000389840 L2458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:7701999 G>A maps to NM_020877.2 E2841E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:7702524 C>T maps to NM_020877.2 I2888I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:7700819 C>T maps to NM_020877.2 L2684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr17:7722540 C>T maps to NM_020877.2 C3610C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr17:7722573 C>A maps to NM_020877.2 L3621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr17:7721268 G>C maps to NM_020877.2 L3414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:7673954 C>G maps to NM_020877.2 L1393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr17:7680152 G>A maps to NM_020877.2 L1668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr17:7674652 C>T maps to NM_020877.2 I1456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr17:7695371 C>T maps to NM_020877.2 G2346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr17:7689455 T>A maps to NM_020877.2 V2048V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:7636550 G>A maps to NM_020877.2 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr16:21073925 C>T maps to NM_017539.1 L1199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr16:21069496 G>A maps to NM_017539.1 V1278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:21063187 G>A maps to NM_017539.1 A1347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:21086797 C>T maps to NM_017539.1 V1018V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:21136610 G>C maps to NM_017539.1 S430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr16:20975224 A>G maps to NM_017539.1 N3327N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr16:21133385 G>A maps to NM_017539.1 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr16:20999095 C>T maps to NM_017539.1 S2267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:20999080 G>C maps to NM_017539.1 V2272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:21115864 C>A maps to NM_017539.1 E765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:20975263 G>A maps to NM_017539.1 I3314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:20996880 C>A maps to NM_017539.1 E2395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr16:21042570 G>A maps to NM_017539.1 I1745I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr16:20975341 G>A maps to NM_017539.1 D3288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr16:21078641 C>T maps to NM_017539.1 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:20975125 G>A maps to NM_017539.1 N3360N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:21151925 G>T maps to NM_017539.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:21110071 C>T maps to NM_017539.1 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:20975167 G>A maps to NM_017539.1 I3346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:20996931 C>A maps to NM_017539.1 E2378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr16:20986703 G>A maps to NM_017539.1 Q2704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr16:20944670 T>C maps to NM_017539.1 K4052K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr5:13780975 G>A maps to NM_001369.2 F2971F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr5:13700902 G>A maps to NM_001369.2 D4523D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr5:13792243 C>T maps to NM_001369.2 L2769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:13865841 A>G maps to NM_001369.2 Y1430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr5:13737393 G>A maps to NM_001369.2 Q3808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr5:13913869 G>A maps to NM_001369.2 D506D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr5:13913929 G>A maps to NM_001369.2 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr5:13823434 G>C maps to NM_001369.2 L2208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr5:13708300 G>A maps to NM_001369.2 I4423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr5:13844960 G>C maps to NM_001369.2 V1752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr5:13830161 G>A maps to NM_001369.2 N2074N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr5:13701545 C>A did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr5:13894898 G>C maps to NM_001369.2 S764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr5:13916455 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:13862844 G>A maps to NM_001369.2 I1536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr5:13753589 G>A maps to NM_001369.2 L3542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr5:13862766 G>A maps to NM_001369.2 F1562F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr5:13923436 G>A maps to NM_001369.2 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr5:13759059 G>A maps to NM_001369.2 L3438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr5:13721339 G>A maps to NM_001369.2 I4016I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr5:13781026 C>A maps to NM_001369.2 L2954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr5:13839556 C>T maps to NM_001369.2 K1930K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr5:13901513 G>A maps to NM_001369.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr5:13866330 G>A maps to NM_001369.2 Q1372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr2:84806794 C>T maps to NM_001370.1 Q741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr2:84811349 G>C maps to NM_001370.1 V819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:84806721 A>G maps to NM_001370.1 A716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr2:84804493 A>T maps to NM_001370.1 R680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr2:84780157 G>A maps to NM_001370.1 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr2:196722317 C>A maps to NM_018897.2 E2733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr2:196865505 G>A maps to NM_018897.2 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:196636428 C>T maps to NM_018897.2 L3796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:196877530 G>A maps to NM_018897.2 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:196729193 G>C maps to NM_018897.2 V2395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:196718189 C>T maps to NM_018897.2 E2886E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr2:196729559 G>A maps to NM_018897.2 F2273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:196740420 G>A maps to NM_018897.2 I2088I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:196849370 T>C maps to NM_018897.2 E606E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr2:196718120 G>A maps to NM_018897.2 L2909L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr2:196698975 A>G maps to NM_018897.2 P3018P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr6:38819420 G>T maps to ENST00000327475 G1801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:38957822 C>T maps to ENST00000327475 F4351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr6:38794052 G>A maps to ENST00000327475 L1311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr6:38810630 T>C maps to ENST00000327475 L1587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:38743528 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:38840388 G>A maps to ENST00000327475 T2344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr6:38941540 A>T maps to ENST00000327475 V4198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr6:38867555 C>A maps to ENST00000327475 S3011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr6:38875730 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr6:38883065 G>A maps to ENST00000327475 V3339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr6:38893922 C>G maps to ENST00000327475 L3673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr6:38743561 T>C maps to ENST00000327475 Y587Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr6:38835878 G>A maps to ENST00000327475 L2233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr6:38854692 C>T maps to ENST00000327475 R2784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr6:38957804 G>A maps to ENST00000327475 K4345K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr6:38705720 G>C maps to ENST00000327475 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr6:38980097 G>C maps to ENST00000327475 L4481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr6:38885055 A>G maps to ENST00000327475 A3382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr17:11572853 G>A maps to NM_001372.3 G1032G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:11522878 C>G maps to NM_001372.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:11648334 C>T maps to NM_001372.3 F2111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:11725279 C>T maps to NM_001372.3 I2917I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr17:11666909 C>G maps to NM_001372.3 G2383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr17:11648244 G>A maps to NM_001372.3 K2081K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr17:11607638 C>G maps to NM_001372.3 L1757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr17:11806136 G>A maps to NM_001372.3 E3836E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr9:34514408 C>T maps to NM_012144.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr9:34517425 C>T maps to NM_012144.2 I654I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr9:34512189 C>T maps to NM_012144.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr9:34517359 C>G maps to NM_012144.2 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr9:34501150 G>A maps to NM_012144.2 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:72285871 C>T maps to NM_023036.4 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:72308332 G>A maps to NM_023036.4 K562K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:72297243 C>T maps to NM_023036.4 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr17:72285797 T>A maps to NM_023036.4 L178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr9:33034304 G>A maps to NM_001539.2 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:47005477 C>A maps to NM_005880.3 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr15:78566537 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr15:78566602 C>T maps to NM_018602.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr15:78566698 C>T maps to NM_018602.3 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr15:78557110 G>A maps to NM_018602.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr19:14627646 G>A maps to NM_006145.1 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr3:186302325 C>T maps to NM_016306.4 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:186299203 G>A maps to NM_016306.4 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:74114727 C>T maps to NM_017626.4 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr10:74098042 C>T maps to NM_017626.4 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr10:74095689 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr10:74114613 G>A maps to NM_017626.4 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:73681095 C>T maps to NM_153614.2 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr4:100867638 G>A maps to NM_001031723.2 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr2:220147643 G>A maps to NM_006736.5 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr2:220145383 C>T maps to NM_006736.5 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr1:78470866 C>T maps to NM_007034.3 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:78481926 C>G maps to NM_007034.3 S337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr9:34993316 G>A maps to NM_001135005.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:34997057 C>A maps to NM_001135005.1 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr9:34996274 C>T maps to NM_001135005.1 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr7:157160088 A>G maps to NM_058246.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:157177651 G>T maps to NM_058246.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr7:157177702 G>T did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr22:41257776 G>A maps to NM_145174.1 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:108213697 G>A maps to NM_012328.2 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr10:22208773 C>A maps to NM_022365.3 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:183640137 G>A maps to NM_018981.1 K787K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:6697332 C>A maps to NM_018198.3 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:6696216 C>T maps to NM_018198.3 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr1:6704688 C>T maps to NM_018198.3 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:6741079 C>A maps to NM_018198.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr10:69571356 G>A maps to NM_021800.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:132211336 C>T maps to NM_015268.3 Q1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr3:132235270 C>T maps to NM_015268.3 Q1831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr3:132181318 C>A maps to NM_015268.3 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:132185189 G>A maps to NM_015268.3 E672E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:132215490 C>T maps to NM_015268.3 F1380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr3:132230062 G>A maps to NM_015268.3 L1756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr3:132247061 C>G maps to NM_015268.3 L2137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr3:132207200 C>T maps to NM_015268.3 I1109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr3:132172487 G>T maps to NM_015268.3 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr3:132169585 C>G maps to NM_015268.3 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr3:132257124 G>A maps to NM_015268.3 *2244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr3:132226190 A>G maps to NM_015268.3 Q1703Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:56215781 C>G maps to NM_032364.5 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr12:56221697 G>A maps to NM_032364.5 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr13:43643081 G>A maps to NM_013238.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr1:15870927 G>A maps to NM_015291.2 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr1:15870966 C>T maps to NM_015291.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:15890789 C>T maps to NM_015291.2 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:15892464 C>T maps to NM_015291.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:15894521 C>A maps to NM_015291.2 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr1:15886127 G>C maps to NM_015291.2 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr7:102960100 G>A maps to NM_014377.1 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr12:49743188 C>T maps to NM_024902.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:31447883 G>T maps to NM_181706.4 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr2:25180825 G>A maps to NM_016544.2 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr2:25194755 C>T maps to NM_016544.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr13:96409942 C>T maps to NM_006260.4 Q147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr13:96375562 A>T maps to NM_006260.4 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr13:96438197 C>T maps to NM_006260.4 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr7:73097378 G>A maps to NM_032317.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr11:64000220 C>T maps to NM_005528.3 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr8:67012264 G>C maps to NM_033105.4 *200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:27501156 G>A maps to NM_173650.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr1:65849956 C>T maps to ENST00000371069 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr1:65854978 C>T maps to ENST00000371069 Q412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr1:65871787 C>T maps to ENST00000371069 N821N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr1:65858196 C>T maps to ENST00000371069 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:65849922 C>T maps to ENST00000371069 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:65871610 G>A maps to ENST00000371069 P762P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:65849993 C>A maps to ENST00000371069 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr17:40169377 G>A maps to NM_003315.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:40169362 C>T maps to NM_003315.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr17:40148406 C>T maps to NM_003315.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr10:75005769 G>A maps to NM_015190.3 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:75006493 G>A maps to NM_015190.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:75005765 G>A maps to NM_015190.3 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr23:153631495 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:2286828 C>T maps to NM_001374.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:2287903 C>G maps to NM_001374.2 S243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr3:58178461 G>A maps to NM_004944.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:58196495 C>T maps to NM_004944.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:58186732 C>T maps to NM_004944.2 W179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr3:58194030 G>A maps to NM_004944.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr19:12991619 C>T maps to NM_001375.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:84867739 A>G maps to NM_021233.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:140052880 C>T maps to NM_194249.2 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr5:140052114 G>A maps to NM_194249.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr2:230272011 C>T maps to NM_139072.3 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:230341867 G>A maps to NM_139072.3 Q417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr2:230456364 C>T maps to NM_139072.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:230377517 G>A maps to NM_139072.3 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr11:6532653 C>T maps to NM_144666.2 R463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr11:6592101 C>T maps to NM_144666.2 Q4454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:130981397 C>T maps to ENST00000372923 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr9:131010867 G>T maps to ENST00000372923 E638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr12:32873664 C>T maps to ENST00000381000 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:32866192 C>T maps to ENST00000381000 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr19:10897323 G>T maps to NM_001005361.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:10897349 C>T maps to NM_001005361.2 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:10886553 C>T maps to NM_001005361.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr19:10916621 G>A maps to NM_001005361.2 K508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr19:10883299 A>G maps to NM_001005361.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr19:10912998 C>T maps to NM_001005361.2 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr19:10916640 C>T maps to NM_001005361.2 Q515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:10906751 C>T maps to NM_001005360.2 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr19:10916633 C>T maps to NM_001005361.2 I512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:10939860 C>T maps to NM_001005361.2 I736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:10941027 C>G maps to NM_001005361.2 P839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:172357751 A>G maps to ENST00000359070 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:172017793 C>G maps to ENST00000359070 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr10:101715547 C>T maps to ENST00000342239 K561K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:101639648 G>T maps to ENST00000342239 L1513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr10:101716852 G>C maps to ENST00000342239 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:101716847 G>C maps to ENST00000342239 S128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr10:101637012 G>A maps to ENST00000342239 L1567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr19:10265425 G>A maps to NM_001130823.1 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:10246919 G>A maps to NM_001130823.1 L1511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:10250948 G>A maps to NM_001130823.1 F1193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr19:10267136 G>A maps to NM_001130823.1 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr19:10291224 G>T maps to NM_001130823.1 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr19:10262139 T>C maps to NM_001130823.1 K733K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr2:25469552 G>A maps to NM_175629.1 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr2:25457183 G>A maps to NM_175629.1 L901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr2:25523025 C>T maps to NM_175629.1 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr2:25458691 G>A maps to NM_175629.1 F827F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:25472525 C>T maps to NM_153759.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr2:25457234 C>T maps to NM_175629.1 A884A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr21:45681065 G>C maps to NM_013369.2 S26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr21:45666348 C>T maps to NM_013369.2 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr21:45670791 T>C maps to NM_013369.2 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:220251130 C>T maps to NM_012100.2 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr10:98064409 C>T maps to NM_004088.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr10:98079146 G>A maps to NM_004088.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr20:44439564 C>A maps to NM_052951.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr20:44424003 G>C maps to NM_052951.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:94343391 C>T maps to NM_014597.4 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:94337723 C>G maps to NM_014597.4 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr16:30018384 C>T maps to NM_003586.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr16:30021405 G>A maps to NM_003586.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:128923777 C>T maps to ENST00000398025 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr10:128841363 C>T maps to ENST00000398025 Q692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr10:128925982 C>T maps to ENST00000398025 T913T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr10:128840894 C>T maps to ENST00000398025 Q652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:225751217 T>A maps to NM_014689.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr2:225651828 G>A maps to NM_014689.2 D1855D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:225738787 G>T maps to NM_014689.2 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:225739014 G>A maps to NM_014689.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:117722119 G>A did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr23:117788596 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:117679987 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:117761529 G>A did not map to a codon.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr23:117770338 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr23:117814456 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr23:117743311 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:117815187 T>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:117788638 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr23:117758545 A>G did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr23:117817072 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr5:169507183 G>A maps to NM_004946.2 E1728E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:169122854 C>T maps to NM_004946.2 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:169469045 C>T maps to NM_004946.2 V1262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr5:169463547 G>A maps to NM_004946.2 E1218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr5:169463517 G>C did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr5:169122826 C>G maps to NM_004946.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr5:169101350 G>C maps to NM_004946.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr5:169267849 T>A maps to NM_004946.2 I931I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr5:169096310 C>G maps to NM_004946.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr5:169143251 C>T maps to NM_004946.2 I659I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr5:169507228 C>G maps to NM_004946.2 L1743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr3:51101877 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr3:51266208 A>T maps to NM_004947.4 K589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:51317568 C>T maps to NM_004947.4 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:51418782 C>T maps to NM_004947.4 V1962V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr3:51112864 T>C maps to NM_004947.4 Y181Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr3:51184033 G>A maps to NM_004947.4 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr7:111379264 G>T maps to ENST00000428084 S1719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:111541795 C>T maps to ENST00000428084 K418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:111400252 G>A maps to ENST00000428084 F1382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:111541854 C>A maps to ENST00000428084 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr7:111580177 G>A maps to ENST00000428084 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr7:111368415 G>A maps to ENST00000428084 R1948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr7:111368599 C>T maps to ENST00000428084 P1886P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr7:111398778 C>A maps to ENST00000428084 P1410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr8:25234818 A>G did not map to a codon.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr8:25181400 C>T maps to NM_024940.6 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr8:25203030 C>T maps to NM_024940.6 L886L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-4Z-AA7M-01A-11D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:11323950 C>T maps to ENST00000319867 L1464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr19:11313295 C>T maps to ENST00000319867 S1777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr19:11325226 A>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:62943448 G>A maps to ENST00000371140 F1852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:62993830 G>A maps to ENST00000371140 L1309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr1:62970399 G>A maps to ENST00000371140 L1555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr9:340276 G>A maps to NM_203447.3 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr9:434791 G>A maps to NM_203447.3 K1632K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:422090 G>A maps to NM_203447.3 K1399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:429847 C>T maps to NM_203447.3 A1540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:377194 C>T maps to NM_203447.3 V808V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr9:372261 C>T maps to NM_203447.3 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr9:336615 C>A maps to NM_203447.3 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:429826 C>G maps to NM_203447.3 L1533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr9:336579 A>T did not map to a codon.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr9:429742 C>T maps to NM_203447.3 F1505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr9:428427 C>T maps to NM_203447.3 L1469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr9:428429 G>A maps to NM_203447.3 L1469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr9:439364 C>T maps to NM_203447.3 Q1734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr9:340195 C>T maps to NM_203447.3 I518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr9:441371 C>G maps to NM_203447.3 L1770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr13:99452628 C>T maps to ENST00000428223 K1957K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr13:99520265 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr13:99452658 G>A maps to ENST00000428223 I1947I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr13:99532220 G>T maps to ENST00000428223 Y958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr13:99537284 G>A maps to ENST00000428223 I774I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr13:99489836 G>A maps to ENST00000428223 L1386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr2:74784210 G>A maps to NM_001381.3 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:74783530 G>T maps to NM_001381.3 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr8:21767042 G>A maps to NM_003974.2 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr8:21767042 G>A maps to NM_003974.2 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr5:176936499 G>T maps to NM_024872.2 Y70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr16:57508775 G>A maps to NM_018110.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr18:67365703 G>A maps to NM_152721.5 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMW-01A-11D-A42E-08 chr18:67345051 C>A maps to NM_152721.5 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:3465125 G>A maps to ENST00000389653 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:131709435 G>C maps to NM_014908.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:131709108 C>T maps to NM_014908.3 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:131843463 C>T maps to NM_020438.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr6:31938206 C>T maps to NM_005510.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr6:31939431 C>T maps to NM_005510.3 K7K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:31938784 C>A maps to NM_005510.3 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr21:34951850 C>T maps to NM_017613.2 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr21:34953733 G>A maps to NM_017613.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr21:34951766 C>T maps to NM_017613.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr6:83848137 C>T maps to NM_015018.2 L1459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr6:83877884 G>A maps to NM_015018.2 *2466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr6:83841921 T>C maps to NM_015018.2 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr6:83839158 C>G maps to NM_015018.2 S758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr6:83848843 C>T maps to NM_015018.2 Q1695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr6:83848596 T>A maps to NM_015018.2 S1612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:83848843 C>T maps to NM_015018.2 Q1695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr6:83847183 G>A maps to NM_015018.2 K1141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr6:83838958 C>G maps to NM_015018.2 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr21:37665709 C>T maps to NM_005128.2 F2246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr21:37595609 C>G maps to NM_005128.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr21:37571420 C>T maps to NM_005128.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr21:37642412 C>T maps to NM_005128.2 Q1864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr21:37603049 C>T maps to NM_005128.2 S656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr21:37618603 G>A maps to NM_005128.2 L1442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr21:37665827 G>T maps to NM_005128.2 E2286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr21:37665691 C>T maps to NM_005128.2 I2240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr21:37665712 C>T maps to NM_005128.2 F2247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr21:37586780 C>T maps to NM_005128.2 D352D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr21:37650590 G>A maps to NM_005128.2 R1969R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr21:37600117 C>T maps to NM_005128.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr21:37618315 C>G maps to NM_005128.2 V1346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr21:37617892 C>T maps to NM_005128.2 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr21:37581180 G>T maps to NM_005128.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr21:37584326 C>G maps to NM_005128.2 S279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr21:37618359 C>G maps to NM_005128.2 S1361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr21:37602932 G>A maps to NM_005128.2 W617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr21:37605252 G>A maps to NM_005128.2 K834K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr21:37618231 C>T maps to NM_005128.2 L1318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr19:2213578 C>T maps to ENST00000221482 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr19:2213554 C>T maps to ENST00000221482 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:2210631 G>T maps to ENST00000221482 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:2213596 G>A maps to ENST00000221482 Q539Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:2213855 G>A maps to ENST00000221482 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:2216698 G>A maps to ENST00000221482 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:2216302 G>A maps to ENST00000221482 K649K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:2216318 G>T maps to ENST00000221482 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr19:2222098 C>T maps to ENST00000221482 T977T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:2208971 C>T maps to ENST00000221482 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:2213963 C>A maps to ENST00000221482 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:2222506 C>T maps to ENST00000221482 V1113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:2222185 C>G maps to ENST00000221482 L1006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:2226779 C>G maps to ENST00000221482 L1420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:2222542 C>T maps to ENST00000221482 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:2216761 G>A maps to ENST00000221482 S802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:2217019 G>C maps to ENST00000221482 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:2214471 C>G maps to ENST00000221482 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr11:118968194 G>A maps to NM_001382.3 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr11:118968248 C>T maps to NM_001382.3 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr11:118968637 G>A maps to NM_001382.3 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr11:118967722 G>C maps to NM_001382.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr11:118967722 G>C maps to NM_001382.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr11:118972284 G>C maps to NM_001382.3 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:118972317 G>A maps to NM_001382.3 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr16:89703950 C>T maps to NM_004413.3 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr16:89696853 C>G maps to NM_004413.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr16:68024028 C>T maps to NM_022355.2 K305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr16:68021778 C>T maps to NM_022355.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr16:68021534 G>A maps to NM_022355.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr16:68009901 C>A maps to NM_022357.3 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr16:68010123 G>A maps to NM_022357.3 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr16:68009694 G>A maps to NM_022357.3 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr16:68009820 G>A maps to NM_022357.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr16:68011732 C>A did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr16:68010678 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr16:68011251 C>T maps to NM_022357.3 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:68012511 G>A maps to NM_022357.3 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:38709683 G>A maps to NM_001135155.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:38713254 G>A maps to NM_001135155.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr19:38703010 G>A maps to ENST00000416611 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr19:38713042 G>C maps to NM_001135155.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr11:65113141 G>T maps to NM_006268.3 G215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr11:65113159 C>T maps to NM_006268.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr14:73138023 C>T maps to NM_012074.3 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr14:73159897 G>A maps to NM_012074.3 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr17:1936946 G>A maps to NM_001383.3 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr17:1939320 G>T maps to NM_001383.3 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr17:1939335 G>A maps to NM_001383.3 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr17:1944475 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr1:44437341 G>A maps to NM_001384.4 K256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:44435912 G>A maps to NM_001384.4 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr1:101490987 G>A maps to NM_015958.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr1:101456176 C>T maps to NM_015958.2 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr1:155112685 G>A maps to NM_018973.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:155112690 C>T maps to NM_018973.3 W39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:116485504 A>G maps to NM_020868.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:116066831 C>T maps to NM_020868.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:116447416 G>T maps to NM_020868.3 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr2:116535410 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr2:116599836 C>G maps to NM_020868.3 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr2:116525964 T>C maps to NM_020868.3 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:116548708 G>A maps to NM_020868.3 K528K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr2:116066897 C>T maps to NM_020868.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr2:116257165 G>T maps to NM_020868.3 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:66272177 C>T maps to NM_005700.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr2:162873276 C>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr7:154672606 G>A maps to NM_130797.2 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr7:154561136 G>A maps to NM_130797.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr7:154595662 G>A maps to NM_130797.2 K499K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr7:154684051 G>A maps to NM_130797.2 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:154598702 G>T did not map to a codon.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr7:154564586 C>T maps to NM_130797.2 H357H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr9:140006400 G>T maps to NM_013379.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr15:65759414 G>A maps to NM_197960.2 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr15:65808021 C>T maps to NM_197960.2 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr15:65792943 C>T maps to NM_197960.2 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr19:4683569 C>G maps to ENST00000357909 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:4700227 C>T maps to ENST00000357909 K437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr3:109031404 C>T maps to NM_138815.3 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr12:7864222 C>T maps to NM_199286.2 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:109050828 C>T maps to NM_018189.3 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr3:109046870 C>T maps to NM_018189.3 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr3:109052768 T>A maps to NM_018189.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr6:74063702 G>A maps to NM_001025290.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:54139968 G>C maps to NM_001012728.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr19:54140100 T>A maps to NM_001012728.1 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr19:54140181 C>T maps to NM_001012728.1 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:168683487 G>C maps to NM_001937.4 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr12:64020260 G>A maps to NM_173812.4 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr19:32930032 A>G maps to NM_001172774.1 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr8:95802119 G>A maps to NM_181787.2 V718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:32264362 G>C maps to ENST00000452582 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:32264362 G>A maps to ENST00000452582 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr1:97771775 T>G maps to NM_000110.3 P712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr1:98205965 G>A maps to NM_000110.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr1:97839178 C>A maps to NM_000110.3 E666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:98039505 T>C maps to NM_000110.3 E383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr1:98060675 C>T maps to NM_000110.3 Q299Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr1:97848005 A>C maps to NM_000110.3 A639A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr1:98015253 T>C maps to NM_000110.3 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr8:105441798 G>A maps to NM_001385.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:105456548 C>A maps to NM_001385.2 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr8:105463491 C>T maps to NM_001385.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr8:105405046 C>A maps to NM_001385.2 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr8:105463581 C>T maps to NM_001385.2 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr8:26484808 G>T maps to NM_001197293.1 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr5:146778785 G>A maps to NM_001197294.1 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr10:134018388 C>T maps to NM_006426.2 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr10:134006278 C>A maps to NM_006426.2 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr10:134013860 G>A maps to NM_006426.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr10:134014487 G>C did not map to a codon.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr2:27121540 G>A maps to NM_020134.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr2:27162913 C>T maps to NM_020134.3 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:74749804 G>C maps to NM_133637.2 S466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr2:74749884 C>T maps to NM_133637.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr2:74751325 A>G maps to NM_133637.2 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:93812390 G>A maps to NM_001938.2 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:102314992 G>C did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:102315036 G>A maps to NM_018370.2 *239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:111674047 G>A maps to NM_178454.4 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr5:174869070 G>C maps to NM_000794.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr5:174868815 G>A maps to NM_000794.3 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr11:113286177 G>A maps to ENST00000355319 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr11:113295145 G>A maps to ENST00000355319 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:113286259 G>A maps to ENST00000355319 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr11:113283434 C>T maps to ENST00000355319 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:113850097 C>T maps to NM_000796.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:113847751 G>A maps to NM_000796.3 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr4:9784852 C>T maps to NM_000798.4 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr4:9784852 C>A maps to NM_000798.4 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr4:9784900 C>T maps to NM_000798.4 N416N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr4:9783853 G>A maps to NM_000798.4 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr4:9783919 C>T maps to NM_000798.4 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr4:9783892 C>T maps to NM_000798.4 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr22:31816284 G>A maps to NM_004147.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr17:18005254 G>A maps to NM_001388.3 Q250Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr17:18003718 C>T maps to NM_001388.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:50599214 G>A maps to NM_001080520.1 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:100497934 C>T did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr23:100513301 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr23:100509501 G>A did not map to a codon.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr23:100503111 C>T did not map to a codon.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr23:100492730 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:100497373 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:100490870 C>T did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:100497445 T>A did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr18:28737510 C>G maps to NM_024421.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr18:28710777 C>G maps to NM_004948.3 L837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr18:28714067 C>T maps to NM_024421.2 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr18:28737510 C>G maps to NM_024421.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr18:28737470 G>A maps to NM_024421.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr18:28648097 T>C maps to ENST00000438199 G876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr18:28672096 C>T maps to ENST00000438199 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr18:28654727 G>A maps to ENST00000438199 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr18:28611014 G>T maps to NM_001941.3 S93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr18:28581658 C>G maps to NM_001941.3 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr18:28576943 G>C maps to NM_001941.3 S769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr18:28612236 G>A maps to NM_001941.3 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FH-01A-11D-A38G-08 chr18:28611031 C>T maps to NM_001941.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr21:42080496 G>A maps to NM_001389.3 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr21:41447092 G>A maps to NM_001389.3 L1587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr21:41457655 C>T maps to NM_001389.3 R1335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr21:41496163 G>A maps to NM_001389.3 I1218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:41741076 G>A maps to NM_001389.3 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr21:41711076 G>A maps to NM_001389.3 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr21:42218551 G>A maps to NM_001389.3 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr21:41452088 G>T maps to NM_001389.3 T1470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr21:41710046 G>A maps to NM_001389.3 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr21:41725467 C>T maps to NM_001389.3 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr21:41668000 G>T maps to NM_001389.3 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr11:117389265 G>A maps to NM_020693.2 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:117307859 G>A maps to NM_020693.2 F1626F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:117391941 G>T maps to NM_020693.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:117306393 C>T maps to NM_020693.2 K1674K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:117352704 G>A maps to NM_020693.2 N904N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr11:117299106 C>G maps to NM_020693.2 S2093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr8:120859262 G>A maps to NM_024094.2 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr21:38600635 G>A maps to NM_006052.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr21:38390384 A>T maps to NM_018962.2 K151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr6:116757644 C>T maps to NM_013352.2 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr18:65180300 C>T maps to NM_032160.2 W525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr18:65180489 C>T maps to NM_032160.2 Q462Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr18:65181722 C>T maps to NM_032160.2 Q51Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr18:28919962 C>G maps to NM_001942.2 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr18:28935011 G>C maps to NM_001942.2 V951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr18:28916509 C>G maps to NM_001942.2 S400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr18:28934969 G>C maps to NM_001942.2 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:29102103 G>A maps to NM_001943.3 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr18:29111174 C>T maps to NM_001943.3 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr18:29116270 A>G maps to NM_001943.3 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr18:29121246 G>A maps to NM_001943.3 W657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr18:29111071 G>A maps to NM_001943.3 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr18:29049226 T>G maps to NM_001944.2 P604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr18:29038997 C>T maps to NM_001944.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr18:29055782 A>T maps to NM_001944.2 K854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr18:28956888 C>T maps to NM_001134453.1 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr18:28989424 C>G maps to NM_001134453.1 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr20:35396440 G>C maps to NM_001145315.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:7581075 G>A maps to NM_004415.2 V1551V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:7583090 C>T maps to NM_004415.2 Q1866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr6:7583744 C>T maps to NM_004415.2 Q2084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr6:7580190 C>G maps to NM_004415.2 L1256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr6:7565680 C>T maps to NM_004415.2 C289C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr6:7583320 C>A maps to NM_004415.2 L1942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr6:7559513 C>T maps to NM_004415.2 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr6:7567655 C>T maps to NM_004415.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:7570714 C>T maps to NM_004415.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr6:7585150 C>T maps to NM_004415.2 L2552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:7583212 C>T maps to NM_004415.2 I1906I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:7583434 C>G maps to NM_004415.2 L1980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:7584133 C>T maps to NM_004415.2 I2213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:7584625 C>A maps to NM_004415.2 I2377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:7584709 C>T maps to NM_004415.2 L2405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:7584877 C>T maps to NM_004415.2 L2461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:7584895 C>T maps to NM_004415.2 V2467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:7585150 C>T maps to NM_004415.2 L2552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:7585225 C>G maps to NM_004415.2 V2577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:7580472 G>A maps to NM_004415.2 K1350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:7580746 C>T maps to NM_004415.2 Q1442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:7583908 G>C maps to NM_004415.2 V2138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr4:88534105 C>T maps to NM_014208.3 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr4:88533841 C>T maps to NM_014208.3 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr6:56397221 G>A maps to ENST00000361203 P5465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr6:56401660 C>T maps to ENST00000361203 Q5351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr6:56482861 C>T maps to ENST00000281662 L2554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:56334712 G>A maps to ENST00000361203 Q7269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr6:56458792 G>A maps to ENST00000361203 L3921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:56417395 G>A maps to ENST00000361203 F5187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:56418127 C>T maps to ENST00000361203 V4943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr6:56342267 C>A maps to ENST00000361203 E6973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr6:56504130 C>A maps to ENST00000361203 E753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr6:56500397 G>A maps to ENST00000361203 Q848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr6:56350148 T>G maps to ENST00000361203 G6845G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr6:56464868 C>A maps to ENST00000361203 E3687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr6:56347627 C>T maps to ENST00000361203 L6874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr6:56496743 C>T maps to ENST00000361203 Q1089Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:56492864 G>A maps to ENST00000361203 Q1313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:56496822 G>C maps to ENST00000361203 S1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:56505345 G>A maps to ENST00000361203 Y484Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr6:56323850 G>C maps to ENST00000361203 P7528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr6:56485188 C>A maps to ENST00000281662 E1779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:56357770 G>A maps to ENST00000361203 L6626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:56336934 C>T maps to ENST00000370754 V5241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:56420410 C>T maps to ENST00000361203 L4745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr6:56417487 G>A maps to ENST00000361203 Q5157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr20:17587721 C>T maps to NM_006870.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr1:205132856 G>A maps to NM_015375.2 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr1:212245551 G>A maps to NM_016448.2 W344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr18:32418762 C>T maps to NM_001390.4 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:25803617 G>A maps to NM_021907.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr6:15627646 G>A maps to NM_032122.4 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr6:15593313 T>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr15:49935751 G>T maps to NM_001144955.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr15:49917390 C>G maps to NM_001144955.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr5:118264396 C>T maps to NM_173666.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr5:118274973 C>T maps to NM_173666.2 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:113515256 C>T maps to NM_004416.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr7:76132903 G>A maps to NM_020892.2 Q517Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr7:76111939 C>T maps to NM_020892.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:76112461 C>T maps to NM_020892.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr12:58002886 G>T maps to NM_178502.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:58002421 C>T maps to NM_178502.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr12:58002907 G>C maps to NM_178502.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr3:122283455 G>A maps to NM_138287.3 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr3:122289465 C>T maps to NM_138287.3 V700V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr3:122283308 C>T maps to NM_138287.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:58940199 G>A maps to NM_015177.1 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr11:58956680 C>T maps to NM_015177.1 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr11:58972186 C>T maps to NM_015177.1 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr11:58956662 G>A maps to NM_015177.1 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:45445632 C>T maps to NM_175940.1 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:45424172 C>T maps to NM_175940.1 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr15:45453039 C>A maps to NM_175940.1 I1236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr15:45439713 G>A maps to NM_175940.1 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr15:45455842 C>T maps to NM_175940.1 I1454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr15:45401812 C>T maps to NM_014080.4 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr15:45399045 G>A maps to NM_014080.4 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:45386348 C>T maps to NM_014080.4 *1549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr15:45399060 G>A maps to NM_014080.4 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr15:45386826 G>T maps to NM_014080.4 S1486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr15:45386799 G>A maps to NM_014080.4 F1495F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr15:45389562 C>G maps to NM_014080.4 L1240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr15:45387235 G>A maps to NM_014080.4 D1431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr15:45412484 C>T maps to NM_144565.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr15:45412382 G>A maps to NM_144565.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr15:45408926 G>A maps to NM_207581.3 W185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:76818086 G>C maps to NM_001003892.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr17:80019220 G>A maps to NM_022156.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:80018632 C>T maps to NM_022156.3 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:80019229 C>G did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr17:80018776 G>A maps to NM_022156.3 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:80019596 C>T maps to NM_022156.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:80020745 G>A maps to NM_022156.3 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr17:80019838 G>A maps to NM_022156.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr16:68071988 G>T maps to NM_017803.3 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr16:68087473 C>G maps to NM_017803.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr16:68112711 C>T maps to NM_017803.3 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr19:5786497 G>T maps to NM_020175.2 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr19:5787611 G>A maps to NM_020175.2 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr7:107215698 G>A maps to NM_181581.1 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:221879667 C>A maps to NM_007207.3 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:221912582 C>T maps to NM_007207.3 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr2:73993694 G>C maps to NM_003584.2 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr2:73993720 C>T maps to NM_003584.2 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:161719827 C>T maps to NM_007240.1 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:161721655 G>A maps to NM_007240.1 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:35872726 C>G maps to NM_007026.2 S118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr20:30450394 A>G maps to NM_080611.3 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:12630831 G>C maps to NM_030640.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:12630909 G>A maps to NM_030640.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:183948269 G>A maps to NM_080876.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:96809648 G>A maps to NM_004418.3 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:44703919 A>T did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr23:44703470 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr23:44703755 C>A did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr6:348189 C>T maps to ENST00000457386 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:348770 T>C maps to ENST00000457386 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:304647 C>T maps to ENST00000457386 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr1:167096929 C>A maps to NM_001080426.1 Y854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:167097697 G>T maps to NM_001080426.1 G1110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:167097271 C>G maps to NM_001080426.1 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr1:167096884 G>A maps to NM_001080426.1 K839K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr1:167096803 C>T maps to NM_001080426.1 C812C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr1:167064151 G>A maps to NM_001080426.1 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:167096653 C>A maps to NM_001080426.1 C762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:167097676 G>A maps to NM_001080426.1 R1103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr1:167096182 G>A maps to NM_001080426.1 K605K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-E7-A7DV-01A-11D-A339-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr2:241500313 C>T maps to NM_001033575.1 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:241500376 G>T maps to NM_001033575.1 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr17:41847126 G>A maps to NM_004090.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr8:29195958 C>T maps to NM_001394.5 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr8:29207675 C>T maps to NM_001394.5 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr10:112258060 C>A maps to NM_004419.3 S61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr10:112266721 C>G maps to NM_004419.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr10:112266778 C>A maps to NM_004419.3 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:112266754 C>T maps to NM_004419.3 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr10:112269919 G>A maps to NM_004419.3 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr12:89743338 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr12:89744425 G>A maps to NM_001946.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr3:52088319 C>G maps to NM_001947.3 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7N-01A-11D-A391-08 chr3:52088253 G>A maps to NM_001947.3 D218D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:52088013 G>A maps to NM_001947.3 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr3:52088052 G>A maps to NM_001947.3 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr3:52088157 G>C maps to NM_001947.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:1586885 C>G maps to NM_004420.2 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:1586966 G>T maps to NM_004420.2 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr11:1587038 G>A maps to NM_004420.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr23:152915711 C>G did not map to a codon.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr23:152914705 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr23:152915678 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:152915625 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr23:152914727 G>A did not map to a codon.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr15:48626676 G>A maps to NM_001025248.1 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:57669782 G>A maps to NM_001012729.1 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr1:1273368 G>A maps to ENST00000378888 Q568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:1273647 C>G did not map to a codon.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr17:7132984 G>A maps to NM_004422.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr17:7130412 C>T maps to NM_004422.2 E513E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:183883250 C>G maps to NM_004423.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:183888153 G>T maps to NM_004423.3 E588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr3:183885728 C>T maps to NM_004423.3 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr3:183885782 C>T maps to NM_004423.3 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr18:46860153 G>A maps to NM_017653.3 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr18:46889550 C>T maps to NM_017653.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr18:46904946 A>G maps to NM_017653.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr14:102461423 G>A maps to NM_001376.4 Q1145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr14:102514869 C>T maps to NM_001376.4 F4412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr14:102442047 G>C did not map to a codon.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr14:102483750 C>G maps to NM_001376.4 S2696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr14:102477156 G>T maps to NM_001376.4 S2162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr14:102452340 C>T maps to NM_001376.4 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr14:102493552 T>C maps to NM_001376.4 V2938V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr14:102482233 G>A maps to NM_001376.4 T2428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr14:102514235 G>A maps to NM_001376.4 K4363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr14:102466433 G>T maps to NM_001376.4 E1305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr14:102499628 G>A maps to NM_001376.4 K3407K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr14:102511009 C>T maps to NM_001376.4 A4327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr14:102494122 G>T maps to NM_001376.4 S3072S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr14:102492963 G>A maps to NM_001376.4 L2897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr14:102493543 G>C maps to NM_001376.4 L2935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr14:102505825 G>C maps to NM_001376.4 L3846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr14:102446828 G>T maps to NM_001376.4 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr14:102496232 G>T maps to NM_001376.4 L3240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr14:102446262 T>C maps to NM_001376.4 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr7:95457371 C>A maps to NM_004411.4 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr7:95442531 G>A maps to NM_004411.4 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:32582546 T>C maps to NM_016141.3 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr16:66766330 G>C maps to NM_006141.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:66783139 T>A maps to NM_006141.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr11:103270432 C>T maps to NM_001080463.1 R4074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:102980455 C>G maps to NM_001080463.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr11:103086496 G>A maps to NM_001080463.1 L2914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr11:103124074 C>G maps to NM_001080463.1 L3375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:103173928 C>T maps to NM_001080463.1 Q3742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr11:103306750 T>C maps to NM_001080463.1 L4156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr11:103052606 C>T maps to NM_001080463.1 L2157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr11:103349882 G>T maps to NM_001080463.1 E4283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr11:103153798 C>T maps to NM_001080463.1 A3632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr11:103006286 C>T maps to NM_001080463.1 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr2:44036904 G>A maps to NM_001193464.1 *353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr17:56164498 C>T maps to NM_080677.2 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr20:33114080 G>A maps to ENST00000374846 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr6:159057859 C>G maps to NM_006519.2 *114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr23:37705595 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr21:38862513 C>G maps to NM_001396.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr19:40316927 T>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:206822132 C>G maps to NM_003582.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:206821904 G>A maps to NM_003582.2 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr12:4722726 G>A maps to NM_003845.1 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr12:4722801 G>A maps to NM_003845.1 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr2:71748030 G>A maps to NM_001130987.1 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr2:71883289 A>C did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:71791216 C>T maps to NM_001130987.1 I813I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr2:71892339 C>T maps to NM_001130987.1 L1741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:71730409 C>T maps to NM_001130987.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr2:71894599 G>A maps to NM_001130987.1 V1804V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr2:71742874 C>T maps to NM_001130987.1 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:207559579 G>C maps to NM_001093730.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr2:207570578 G>A maps to NM_001093730.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr15:55727165 C>T maps to NM_130810.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr15:55790517 G>A maps to NM_130810.2 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr15:55759359 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:96238295 C>T maps to NM_198968.2 E771E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr13:96293692 C>G maps to NM_198968.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr13:96274733 G>A maps to NM_198968.2 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr13:96246296 T>C maps to NM_198968.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:137790533 C>T maps to NM_173543.2 E522E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr3:137822363 G>T maps to NM_173543.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:108355536 T>G maps to NM_014648.3 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr3:108407450 A>G maps to NM_014648.3 K1094K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr3:108363558 C>T maps to NM_014648.3 Q564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr20:32264923 G>C maps to NM_005225.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr20:32267643 C>T maps to NM_005225.2 Q163Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr20:32268188 G>A maps to NM_005225.2 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr1:23857243 C>T maps to NM_004091.3 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:23847563 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:20490416 C>G maps to NM_001949.3 S385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:20402594 C>T maps to NM_001949.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr8:86089813 G>A maps to ENST00000256117 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:11586616 C>A maps to NM_198256.2 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr2:11586603 C>T maps to NM_198256.2 *282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:77421678 A>G maps to NM_203394.2 C708C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr12:77436962 G>A maps to NM_203394.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr12:77439818 A>G maps to NM_203394.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr11:19252337 C>G maps to NM_024680.2 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:19256465 C>T maps to NM_024680.2 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr11:19256300 T>C maps to NM_024680.2 E252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr11:19252337 C>G maps to NM_024680.2 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr11:19246348 G>A maps to NM_024680.2 A820A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr16:2279639 C>T maps to NM_004424.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr16:2285350 C>T maps to NM_004424.3 I711I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:2273625 G>A maps to NM_004424.3 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr3:121575856 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:121554152 C>T maps to NM_018456.4 F7F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HQ-A5NE-01A-12D-A289-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr5:158223454 C>T maps to NM_024007.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr8:25745417 G>A maps to NM_022659.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr8:25902276 G>A maps to NM_022659.2 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr8:25745426 G>A maps to NM_022659.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr8:25708191 C>T maps to NM_022659.2 Q538Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr10:131761946 G>T maps to ENST00000355311 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr10:131671830 G>A maps to ENST00000355311 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr19:4236931 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr3:73111735 C>T maps to NM_018029.3 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:43636435 C>T maps to NM_001159936.1 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:43637292 G>A maps to NM_001159936.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr23:48382310 G>T did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr13:50235296 C>T maps to NM_032565.3 W143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr10:74899247 G>A maps to NM_001135752.1 Q447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr10:74908078 G>C maps to NM_001135752.1 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr10:74916340 T>C maps to NM_001135752.1 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr10:74896560 C>A maps to NM_001135752.1 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:74908105 C>T maps to NM_001135752.1 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:21605858 C>T maps to NM_001113347.1 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:21605737 G>A maps to NM_001397.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:184009971 C>T maps to NM_014693.3 F866F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr3:183995836 G>A maps to NM_014693.3 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr2:233345139 G>A maps to NM_004826.2 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr2:233346254 G>A maps to NM_004826.2 I650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr2:233349276 G>T maps to NM_004826.2 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr19:39321992 G>C maps to NM_001398.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr6:127611177 G>A maps to NM_001139510.1 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr1:53370431 C>G maps to ENST00000371522 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr1:53387302 G>T maps to ENST00000371522 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr10:135184202 C>T maps to NM_004092.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr1:150483595 C>G maps to ENST00000369049 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:150485786 G>C maps to ENST00000369049 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:150482399 C>T maps to ENST00000369049 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr9:95274342 G>A maps to NM_001393.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr9:95272312 G>A maps to NM_001393.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr9:95277371 G>A maps to NM_001393.3 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr9:95277071 G>A maps to NM_001393.3 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr19:11617115 G>A maps to NM_016581.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr19:11617240 C>A maps to NM_016581.3 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr3:172502561 G>A maps to ENST00000392692 Q598Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr6:139135699 T>C maps to NM_001195037.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr6:139206876 C>T maps to NM_001195037.2 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:139186274 C>T maps to NM_001195037.2 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:139203932 G>A maps to NM_001195037.2 T651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr6:139222120 C>T maps to NM_001195037.2 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr6:139186277 C>T maps to NM_001195037.2 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr23:68836298 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:69176893 C>A did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr23:68836393 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:68836525 C>G did not map to a codon.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr23:69255457 A>G did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr23:69253325 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr23:69253280 G>A did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr23:65824269 C>T did not map to a codon.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr23:65824288 T>A did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr15:74927825 G>C maps to NM_025083.3 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr15:74963866 G>C maps to NM_025083.3 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr15:74948409 C>A did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr16:67918014 C>T maps to NM_014329.3 L1390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr16:67909845 A>T did not map to a codon.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr16:67913802 C>T maps to NM_014329.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr16:67916348 C>T maps to NM_014329.3 I1098I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr16:67912684 C>G maps to NM_014329.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:67918029 C>T maps to NM_014329.3 L1395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr16:67913607 G>C maps to NM_014329.3 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr16:67913802 C>T maps to NM_014329.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:5229558 C>A maps to NM_014674.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr3:5229969 C>T maps to NM_014674.2 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:5246761 G>C maps to NM_014674.2 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr3:5249806 C>T maps to NM_014674.2 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr20:33703304 G>A maps to NM_018217.2 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr20:33719492 T>A maps to NM_018217.2 K266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr20:33711795 G>C maps to NM_018217.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr20:33735052 G>A maps to NM_018217.2 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr20:33735052 G>A maps to NM_018217.2 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:184675861 G>A maps to NM_025191.3 I706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr5:83402641 G>C maps to NM_005711.3 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr5:83362398 A>T maps to NM_005711.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:12292617 G>T maps to NM_001955.4 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr1:41945173 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:41945092 C>T maps to NM_001956.3 W175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr20:57875893 C>T maps to NM_207034.1 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr20:57876609 G>A maps to NM_207034.1 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr4:148406958 C>A maps to NM_001957.3 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr4:148463742 G>C maps to NM_001957.3 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr4:148463667 G>A maps to NM_001957.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr13:78477332 T>C maps to ENST00000377211 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr13:78477359 C>T maps to ENST00000377211 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:93245997 C>A maps to NM_003566.3 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr12:93210089 C>T maps to NM_003566.3 Q605Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr12:93210158 C>T maps to NM_003566.3 E582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr12:93174082 G>A maps to NM_003566.3 L1147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr11:85961446 C>G maps to ENST00000351625 S75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr11:85956303 G>C maps to ENST00000351625 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr6:74229728 A>G maps to NM_001402.5 H7H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr20:62120316 C>A maps to NM_001958.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr20:62129077 G>A maps to NM_001958.2 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr20:62120352 C>T maps to NM_001958.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr20:62120421 C>T maps to NM_001958.2 K371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:144668985 C>T maps to NM_032378.4 K376K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr8:144671789 C>A maps to NM_032378.4 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr8:144662723 C>T maps to NM_032378.4 K554K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr8:144671912 C>T maps to NM_032378.4 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr8:144671270 G>A maps to NM_032378.4 C327C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr19:3977233 G>A maps to NM_001961.3 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:3984132 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:3979970 C>A maps to NM_001961.3 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:3983207 G>T maps to NM_001961.3 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:3982046 G>A maps to NM_001961.3 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr19:3979976 G>A maps to NM_001961.3 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr3:128127100 G>C maps to NM_021937.3 *597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:36327381 G>A maps to NM_030636.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr7:36193941 C>T maps to NM_030636.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr7:36194373 C>T maps to NM_030636.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:36194052 C>G maps to NM_030636.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr7:36336719 C>T maps to NM_030636.2 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr8:49647689 C>T maps to NM_024593.3 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr8:49643940 T>C maps to NM_024593.3 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr17:60493444 C>T maps to NM_001144933.1 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr17:60493411 C>T maps to NM_001144933.1 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:60472494 C>A maps to NM_001144933.1 S197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr12:3765482 C>T maps to NM_001144958.1 Q284Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr17:28384796 G>A maps to NM_198529.3 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:28296146 A>T maps to NM_198529.3 K177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr17:28380459 G>A maps to NM_198529.3 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:28380874 G>T maps to NM_198529.3 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr17:28418976 C>G maps to NM_198529.3 L1342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr17:28405289 C>G maps to NM_198529.3 S932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr17:28405332 C>A maps to NM_198529.3 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr17:28380716 C>G maps to NM_198529.3 S582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:43972200 C>T maps to NM_022785.3 Q1132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr22:44004411 G>A maps to NM_022785.3 Y877Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr22:43976448 C>T maps to NM_022785.3 K1041K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr22:44031096 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr22:44112838 C>T maps to NM_022785.3 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr1:64027422 T>C maps to NM_032437.2 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr2:56108798 G>T maps to NM_001039349.1 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:56144827 G>C maps to NM_001039349.1 Y163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr2:56094294 C>A maps to NM_001039349.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr11:65638715 G>A maps to NM_016938.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr13:22077088 C>G maps to NM_152726.2 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr8:16963024 C>T maps to NM_181723.2 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:19959754 G>A maps to NM_144715.3 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:19975087 C>A maps to NM_144715.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr3:19930020 G>A maps to NM_144715.3 F616F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:52344528 C>T maps to NM_018100.3 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr6:52344501 C>T maps to NM_018100.3 N519N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr23:44108097 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr23:44091781 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr23:44037688 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr23:44089007 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:44120511 G>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr2:233527595 G>T maps to NM_025202.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr1:15736683 C>T maps to NM_024329.5 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:15736622 C>T maps to NM_024329.5 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:155104033 G>A maps to NM_004428.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr23:68060481 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr23:68060459 C>T did not map to a codon.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr23:68060144 C>T did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:68060223 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr13:107145642 C>T maps to NM_004093.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr13:107145675 G>A maps to NM_004093.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:7611545 G>A maps to NM_001406.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr17:7612892 G>A maps to NM_001406.3 *341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:132962329 C>T maps to NM_015137.3 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr8:133014901 G>A maps to NM_015137.3 E753E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr8:133008704 G>A maps to NM_015137.3 Q706Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr8:133014901 G>A maps to NM_015137.3 E753E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr8:132957120 T>C did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:23828630 G>A maps to NM_005864.2 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr15:82431175 G>A maps to NM_024580.5 V999V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr15:82443992 G>A maps to NM_024580.5 C934C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr15:82545071 G>A maps to NM_024580.5 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr17:42937867 G>A maps to NM_004247.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr17:42942370 C>T maps to NM_004247.3 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:42940196 C>G maps to NM_004247.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr17:42941052 G>A maps to NM_004247.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr17:42930715 G>A maps to NM_004247.3 Q837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr17:42929875 T>C maps to NM_004247.3 K872K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr17:42957997 G>A maps to NM_004247.3 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:110882117 C>T maps to NM_001963.4 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr4:110866375 G>A maps to NM_001963.4 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr4:110932596 G>T maps to NM_001963.4 E1204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr4:110866375 G>A maps to NM_001963.4 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr4:110925664 C>T maps to NM_001963.4 Q1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr4:110885638 C>A maps to NM_001963.4 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr4:110932609 G>T maps to NM_001963.4 *1208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr4:110866294 A>T maps to NM_001963.4 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:13635939 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr23:13607686 C>T did not map to a codon.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr9:139565432 G>A maps to NM_201446.1 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:32134564 C>T maps to NM_030652.2 H104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr5:38370442 G>A maps to ENST00000354891 Q197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr5:38406324 G>A maps to ENST00000354891 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr5:38352433 G>A did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr7:55214317 G>A maps to NM_005228.3 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:55241720 C>T maps to NM_005228.3 F723F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr7:55266488 G>A maps to NM_005228.3 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr19:41307022 C>T maps to NM_053046.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr5:137803553 C>A maps to NM_001964.2 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr5:137801497 C>T maps to NM_001964.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr10:64573653 G>C maps to NM_001136178.1 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr10:64575747 G>A maps to NM_001136178.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr10:64573587 G>A maps to NM_001136178.1 N270N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr8:22548612 G>C maps to NM_004430.2 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr8:22548690 G>C maps to NM_004430.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:73519499 G>A maps to NM_001965.3 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr2:73518587 G>C maps to NM_001965.3 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:73519117 G>A maps to NM_001965.3 Q413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr2:63092085 T>A maps to NM_015252.3 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr11:65349829 G>T maps to NM_001099409.1 E563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr11:65359466 C>T maps to NM_001099409.1 Q1460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:65357661 G>A maps to NM_001099409.1 L1388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr11:65349821 G>A maps to NM_001099409.1 W560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:64627437 G>A maps to NM_006795.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr11:64622200 C>T maps to NM_006795.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:48229177 C>T maps to NM_014601.3 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:48244214 G>A maps to NM_014601.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:48229210 C>T maps to NM_014601.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:48220243 C>G maps to NM_014601.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr19:48244457 G>T maps to NM_014601.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr2:31484564 C>T maps to NM_014600.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr2:31489522 C>T maps to NM_014600.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr2:31457561 C>G maps to NM_014600.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:42202031 C>T maps to NM_139265.3 K318K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr15:42193071 G>C maps to NM_139265.3 S466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr15:42193058 G>A maps to NM_139265.3 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr15:42193055 C>T maps to NM_139265.3 K471K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:34680083 G>A maps to NM_012153.4 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr11:34673323 C>T maps to NM_012153.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr11:34680083 G>C maps to NM_012153.4 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr3:184911021 C>T maps to NM_001966.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr9:140695357 C>T maps to NM_024757.4 I878I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr9:140707936 C>T maps to NM_024757.4 C1045C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr9:140729269 C>T maps to NM_024757.4 F1254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr9:140648654 C>G maps to NM_024757.4 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr9:140705989 C>T maps to NM_024757.4 C930C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr9:140728820 C>T maps to NM_024757.4 I1187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr6:31854611 C>T maps to ENST00000395728 V784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr6:31855423 G>C maps to ENST00000395728 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:31852766 G>A maps to ENST00000395728 I847I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:31854444 G>A maps to ENST00000395728 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr11:125448903 C>T maps to ENST00000278903 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:40030086 C>T maps to NM_153232.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:104698236 C>T maps to NM_001008394.1 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr12:104697750 C>T maps to NM_001008394.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr12:104697732 G>A maps to NM_001008394.1 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr17:39846123 G>A maps to NM_005801.3 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr17:39846393 C>T maps to NM_005801.3 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:40352531 G>A maps to NM_005875.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr7:6086640 T>C maps to NM_014413.3 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:37366872 C>T maps to NM_001135651.1 Q139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr2:37366799 G>A maps to NM_001135651.1 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:37336340 G>C maps to NM_001135651.1 S492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:88874948 G>A maps to NM_004836.5 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:88885438 C>A maps to NM_004836.5 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr2:88874769 G>C maps to NM_004836.5 S744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr2:88874948 G>A maps to NM_004836.5 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr2:88894995 A>G maps to NM_004836.5 Y208Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:88870499 C>G maps to NM_004836.5 V959V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr15:40241432 G>A maps to NM_001013703.2 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr15:40265856 C>T maps to NM_001013703.2 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr15:40241357 C>T maps to NM_001013703.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr15:40268619 G>A maps to NM_001013703.2 Q608Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr12:124109398 C>A maps to NM_001414.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr14:75471446 A>C maps to NM_014239.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr14:75469785 C>T maps to NM_014239.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr2:27591874 G>C maps to NM_172195.3 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:27589788 G>T maps to NM_172195.3 S363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr2:27590686 C>T maps to NM_172195.3 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr3:183860369 G>T maps to NM_003907.2 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:183860564 A>C did not map to a codon.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr3:183854513 G>T maps to NM_003907.2 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr3:183855952 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr3:183862398 C>T maps to NM_003907.2 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr1:36384757 C>T maps to NM_012199.2 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:36360779 C>T maps to NM_012199.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:36372535 G>A maps to NM_012199.2 K466K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:36367598 C>A maps to NM_012199.2 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr8:141561520 C>T maps to NM_012154.3 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr8:141549522 C>A maps to NM_012154.3 E689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr8:141561490 C>T maps to NM_012154.3 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr8:141567304 C>T maps to NM_012154.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr8:141551358 G>A maps to NM_012154.3 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr8:141549463 C>T maps to NM_012154.3 Q708Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr8:141559306 C>T maps to NM_012154.3 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr1:36479584 G>T maps to NM_024852.2 E448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr1:36437642 T>C maps to NM_024852.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr1:36397035 C>T maps to NM_024852.2 I3I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:36301441 G>A maps to NM_017629.2 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:36298148 C>T maps to NM_017629.2 Q453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:36301504 G>A maps to NM_017629.2 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:36306945 C>G maps to NM_017629.2 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:32684518 G>A maps to NM_003908.3 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:24086215 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr23:24084128 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:24073095 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr23:24086204 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:24091328 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr23:24086095 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr10:120817658 G>A maps to NM_003750.2 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:120803573 C>T maps to NM_003750.2 P913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr10:120796679 T>C maps to NM_003750.2 R1290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr10:120830513 G>A maps to NM_003750.2 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:2411473 C>T maps to ENST00000314800 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr7:2403296 G>T maps to ENST00000314800 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr7:2404032 G>A maps to ENST00000314800 W342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr7:2402752 C>T maps to ENST00000314800 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr22:36913460 C>A maps to NM_003753.3 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:109228655 C>T maps to NM_001568.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr8:109240614 C>G maps to NM_001568.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr8:109260901 G>T maps to NM_001568.2 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:8016017 G>A maps to ENST00000449102 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:8013369 C>A maps to ENST00000449102 S151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:39114741 C>T maps to NM_013234.2 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr19:39127541 C>T maps to NM_013234.2 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:39125631 G>A did not map to a codon.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr22:38266267 G>A maps to ENST00000262832 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr22:38266334 G>A maps to ENST00000262832 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr22:38259031 C>T maps to ENST00000262832 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr11:32615423 A>G maps to NM_006360.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:7480705 G>A maps to NM_001416.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr3:186506968 G>T maps to ENST00000440191 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:78110042 C>A maps to NM_014740.3 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:78115613 G>A maps to NM_014740.3 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:78115642 G>A maps to NM_014740.3 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:78111250 G>C maps to NM_014740.3 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:53421929 A>C maps to ENST00000438209 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr12:53433925 G>C did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr12:53412670 C>A maps to ENST00000438209 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr5:176072436 C>T maps to NM_001099408.1 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:233431864 A>G maps to NM_004846.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr2:233428955 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr2:233421128 G>A maps to NM_004846.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:71745637 C>T maps to NM_001134651.1 W126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:72179788 G>T maps to NM_004096.4 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr10:72164228 C>T maps to NM_004096.4 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr22:31884647 C>T maps to NM_019843.3 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr22:31859019 G>A maps to NM_019843.3 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr22:31850317 G>A maps to NM_019843.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr22:31838021 C>T maps to NM_019843.3 Q763Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr3:184041219 C>T maps to NM_001194947.1 Q712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr3:184040228 C>T maps to NM_001194947.1 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:184043094 C>A maps to NM_001194947.1 I972I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr3:184040743 T>G did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr3:184035527 G>T maps to NM_001194947.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:184049735 G>T maps to NM_001194947.1 E1501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:10821760 T>C maps to ENST00000429377 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr11:10821250 C>G maps to ENST00000429377 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:10822516 G>A maps to ENST00000429377 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:10823910 G>A maps to ENST00000429377 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:10825595 G>C maps to ENST00000429377 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:10821736 G>C maps to ENST00000429377 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:21307590 G>A maps to NM_001198801.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:21212780 A>G maps to NM_001198801.1 D759D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr1:21177810 C>A maps to NM_001198801.1 G1218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:21175998 G>C maps to NM_001198801.1 S1246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr1:21329219 G>A maps to NM_001198801.1 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:21268769 G>A maps to NM_001198801.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:21137291 C>T maps to NM_001198801.1 E1541E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:21137339 G>A maps to NM_001198801.1 I1525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:21268329 C>T maps to NM_001198801.1 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr7:73604636 G>A did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr7:73602030 T>G maps to NM_022170.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:73588772 G>A did not map to a codon.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr7:73609544 C>T maps to NM_022170.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:103803036 G>T maps to NM_183004.3 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:103804703 G>A maps to NM_183004.3 K160K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:7214696 C>A maps to NM_001143760.1 S130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:100011208 G>C maps to NM_015904.3 V1039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:99984992 G>A maps to NM_015904.3 K442K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:99993063 G>T maps to NM_015904.3 E603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr2:99995513 C>T maps to NM_015904.3 N625N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:33872045 G>A maps to NM_002212.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr20:33871997 G>A maps to NM_002212.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr20:33872176 G>C maps to NM_181466.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr20:33872188 G>A maps to NM_002212.2 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:48510707 G>T maps to NM_018696.2 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr19:856139 G>A maps to NM_001972.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr19:8038617 G>A maps to ENST00000351593 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr19:8046038 G>A maps to ENST00000351593 Y95Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr19:8038681 C>T maps to ENST00000351593 Q146Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr19:8038739 G>C maps to ENST00000351593 S127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:8028432 C>T maps to ENST00000351593 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7N-01A-11D-A391-08 chr19:11565541 C>T maps to NM_001420.3 W301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr19:11568910 G>A maps to NM_001420.3 Y226Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr19:11591417 G>A maps to NM_001420.3 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr19:11569273 T>A maps to NM_001420.3 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:50666657 T>C maps to NM_021952.3 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:50610765 C>T maps to NM_021952.3 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr1:50642769 T>G maps to NM_021952.3 L87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr13:41515450 G>A maps to NM_172373.3 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr13:41507793 G>A maps to NM_172373.3 Q543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr13:41533089 G>C maps to NM_172373.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr13:41507749 G>A maps to NM_172373.3 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr13:41517239 G>A maps to NM_172373.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr4:139993173 A>C maps to ENST00000379550 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr4:140005338 C>T maps to NM_006874.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr1:201980325 C>A maps to NM_004433.4 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:201981808 C>T maps to NM_004433.4 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr1:201981145 G>A maps to NM_004433.4 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr1:201981083 G>A did not map to a codon.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:129200941 C>A did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr23:129206252 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr23:129208116 C>G did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr23:129203613 C>G did not map to a codon.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr23:129206252 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:129200775 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr23:129206341 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:129203379 G>A did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:37770272 G>A maps to NM_052906.3 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr22:37771106 G>A maps to NM_052906.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr22:37771337 C>T maps to NM_052906.3 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr23:47500812 A>G did not map to a codon.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr23:47500684 C>T did not map to a codon.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr12:96640928 C>G maps to NM_005230.2 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:205589785 G>A maps to NM_001973.2 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:18632760 C>T maps to NM_006532.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr15:44067579 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr15:44067924 C>A maps to NM_025165.2 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:37298856 G>A maps to NM_014800.9 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr7:37355563 T>A maps to NM_014800.9 K27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr7:37298952 A>C maps to NM_014800.9 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr20:45008909 G>C maps to ENST00000439931 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr20:45022240 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:45012096 C>T maps to ENST00000439931 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:67233111 G>A maps to NM_024712.3 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:67237767 C>T maps to NM_024712.3 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr4:141463726 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr4:141458649 G>A maps to NM_153702.3 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:85617503 C>T maps to NM_032213.4 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr2:85604590 C>T maps to NM_001135023.1 H244H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr2:85604470 G>A maps to NM_001135023.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:85590233 G>A maps to NM_001135023.1 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr1:43830025 C>T maps to NM_022821.2 W196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr6:11005634 G>A maps to NM_017770.3 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr10:103987406 G>A maps to NM_152310.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr10:103988840 C>T maps to NM_152310.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr10:103986331 T>C maps to NM_152310.1 H9H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:53138101 G>A maps to ENST00000370918 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr5:60083197 C>T maps to NM_024930.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr5:60067825 T>C maps to NM_024930.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr18:33722263 C>G maps to ENST00000442325 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr18:33744581 C>T maps to ENST00000442325 R701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr18:33744589 G>A maps to ENST00000442325 W703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr18:33734811 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr18:33754519 A>C maps to ENST00000442325 A864A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr8:27954793 G>C maps to NM_018091.5 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr8:27954742 C>T maps to NM_018091.5 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:31648698 G>A maps to ENST00000395934 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:48525556 C>T maps to NM_022142.4 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr19:48511944 C>T maps to NM_022142.4 Y7Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr1:79383665 C>A maps to NM_022159.3 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr1:79387373 G>C maps to NM_022159.3 S394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr1:79383519 G>C maps to NM_022159.3 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:79385972 G>A maps to NM_022159.3 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:79404908 G>T maps to NM_022159.3 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr1:79403907 C>A maps to NM_022159.3 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr1:79470875 G>T maps to NM_022159.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:79385975 G>A maps to NM_022159.3 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:49706753 G>A maps to NM_198449.2 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr23:153609240 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:153608351 G>C did not map to a codon.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr23:153608139 C>G did not map to a codon.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr17:48452830 G>T maps to NM_001166131.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr17:48456575 C>T maps to NM_001166131.1 D420D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr16:1825953 C>G maps to NM_001010865.1 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr22:29627007 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr2:27301965 C>G maps to NM_007046.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr18:2891228 C>T maps to NM_032048.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr18:2892353 G>A maps to NM_032048.2 Q743Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr18:2891873 G>A maps to NM_032048.2 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr18:2913062 A>C did not map to a codon.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr18:2913086 T>C maps to NM_032048.2 D949D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr18:2885066 T>C maps to NM_032048.2 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr20:39991161 C>T maps to NM_052846.1 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr20:39990248 G>A maps to NM_052846.1 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr20:39991631 G>A maps to NM_052846.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr14:100375680 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:100405532 G>T did not map to a codon.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr14:100384168 C>T maps to NM_001008707.1 V620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr14:100317291 C>G maps to NM_001008707.1 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr14:100380514 G>C did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr19:46141892 C>A did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:62376049 G>A maps to ENST00000278845 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:62372640 G>C maps to ENST00000278845 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr11:62376854 T>C maps to ENST00000278845 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr2:42396762 C>T maps to NM_019063.3 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:42488300 G>T maps to NM_019063.3 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:42522290 G>A maps to NM_019063.3 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:42543132 C>T maps to NM_019063.3 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr14:89124636 G>A maps to ENST00000380664 G1257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr14:89171300 G>A maps to ENST00000380664 Q652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr14:89148327 C>T maps to ENST00000380664 L1010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr14:89123765 C>A maps to ENST00000380664 G1320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr16:10637429 G>A maps to NM_001424.4 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr16:10631800 G>A maps to NM_001424.4 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr19:48832669 C>T maps to NM_001425.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:6926453 G>C maps to ENST00000381407 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:6928194 C>T maps to ENST00000381407 F756F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:6928164 G>A maps to ENST00000381407 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:6926453 G>A maps to ENST00000381407 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr19:6926513 C>T maps to ENST00000381407 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:6924747 C>G maps to ENST00000381407 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr19:6913662 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:14863200 C>T maps to NM_013447.2 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr19:14862399 G>A maps to NM_013447.2 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:14758013 C>A maps to NM_032571.3 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr2:73160941 G>A maps to NM_004097.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:73160998 G>A maps to NM_004097.2 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:73161037 G>A maps to NM_004097.2 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr10:119303149 C>A maps to NM_004098.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr10:119303134 C>T maps to NM_004098.3 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:119600618 G>A maps to NM_001426.3 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr2:119604404 C>T maps to NM_001426.3 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr2:119604364 G>A maps to NM_001426.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:119600672 G>A maps to NM_001426.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr4:71508030 C>T maps to NM_031889.2 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr4:71508535 G>T maps to NM_031889.2 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr4:71500194 G>A maps to NM_031889.2 Q127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:73930720 G>A maps to NM_003633.2 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr11:94862451 C>T maps to NM_015036.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr12:48110176 G>A maps to NM_001172439.1 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr12:48110278 G>A maps to NM_001172439.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr12:48111319 C>T maps to NM_001172439.1 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:130592028 G>A maps to NM_001114753.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr9:130605387 G>A maps to NM_001114753.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:130580996 G>A maps to NM_001114753.1 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr9:130581078 G>C maps to NM_001114753.1 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr17:77079566 C>T maps to NM_001042573.1 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr17:77075619 C>T maps to NM_001042573.1 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr17:77082388 C>A maps to NM_001042573.1 A730A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr10:25304826 G>A maps to NM_145010.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:8927304 C>T maps to NM_001428.2 K105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:8932037 G>A maps to NM_001428.2 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr12:7025641 G>A maps to NM_001975.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr12:7030903 C>G maps to NM_001975.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr17:4858862 G>T maps to NM_053013.3 G277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr17:4858804 C>A maps to NM_053013.3 Y257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:4859246 C>T maps to NM_053013.3 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr4:83369071 G>A did not map to a codon.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr13:43935580 G>A maps to NM_001127615.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:43798218 A>C maps to NM_001127615.1 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:129803976 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr23:129771249 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr23:129771261 C>A did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr23:129790590 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr23:129801713 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr23:129801556 A>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:111430910 C>G maps to NM_001977.3 S381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:111452429 G>T maps to NM_001977.3 E602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:111464012 G>A maps to NM_001977.3 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr4:111430913 C>G maps to NM_001977.3 S382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr4:111441438 C>T maps to NM_001977.3 N548N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr4:111430913 C>G maps to NM_001977.3 S382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:132201158 T>C maps to NM_006208.2 Y695Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr6:132203594 C>T maps to NM_006208.2 Y737Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr8:120577109 G>A maps to NM_006209.3 F791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:120631536 C>T maps to NM_006209.3 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr8:120628513 T>G maps to NM_006209.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr8:120620214 T>C maps to NM_006209.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr8:120638955 T>C maps to NM_006209.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr8:120651011 C>T maps to NM_006209.3 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr8:120598529 A>G maps to NM_006209.3 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr8:120606088 A>G maps to NM_006209.3 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr6:131979527 G>A maps to NM_005021.3 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr6:131979501 A>G maps to NM_005021.3 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr6:131971179 G>A maps to NM_005021.3 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:131958568 G>A maps to NM_005021.3 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr6:46129304 G>A maps to NM_021572.4 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr6:46129185 G>A maps to NM_021572.4 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr4:185012380 G>C maps to NM_153343.3 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr4:185012518 G>A maps to NM_153343.3 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr4:185012344 G>C maps to NM_153343.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr17:77708846 G>C maps to NM_178543.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr17:77709074 G>A maps to NM_178543.3 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:77709182 C>T maps to NM_178543.3 H247H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr17:77709309 G>T maps to NM_178543.3 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr17:77711736 A>G maps to NM_178543.3 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr17:77709176 C>T maps to NM_178543.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:150599890 G>A maps to ENST00000369009 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr22:40161510 G>C maps to NM_152512.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr22:40140186 G>A maps to NM_152512.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr22:40139833 C>T maps to NM_152512.3 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr22:40161510 G>A maps to NM_152512.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:97607264 C>T maps to NM_001098175.1 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr10:97625980 G>A maps to NM_001098175.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr10:97624561 C>T maps to NM_001098175.1 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:97605317 C>T maps to NM_001098175.1 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:97605350 C>T maps to NM_001098175.1 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr10:97602248 C>G maps to NM_001098175.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr9:139945380 G>C maps to NM_203468.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr9:139945963 G>A maps to NM_203468.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:139943282 G>C maps to NM_203468.1 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr9:139945801 G>T maps to NM_203468.1 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:40457434 G>A maps to NM_001248.2 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:40464879 G>A maps to NM_001248.2 Q401Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:40453375 C>G maps to NM_001248.2 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr8:23290507 C>T maps to NM_004901.3 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr8:23290507 C>T maps to NM_004901.3 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr20:25203474 G>A maps to NM_001247.2 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:101445632 G>A maps to NM_020354.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr10:101445608 C>G maps to NM_020354.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr9:140332527 G>A maps to NM_001033113.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr3:27760354 G>A maps to ENST00000449599 Y396Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr22:41547873 C>G maps to NM_001429.3 S952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr22:41551099 C>T maps to NM_001429.3 Q1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr22:41574468 G>T maps to NM_001429.3 E2252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr22:41513288 C>T maps to NM_001429.3 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr22:41572403 C>T maps to NM_001429.3 R1645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr22:41573078 C>G maps to NM_001429.3 L1788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr22:41573837 C>G maps to NM_001429.3 L2041L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr22:41573888 C>G maps to NM_001429.3 L2058L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr22:41513765 C>T maps to NM_001429.3 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr22:41547923 G>T maps to NM_001429.3 E969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr22:41513679 C>G maps to NM_001429.3 S195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr22:41566487 G>A maps to NM_001429.3 Q1455Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr22:41537059 C>G maps to NM_001429.3 Y629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr22:41543839 G>A did not map to a codon.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr22:41565611 G>A maps to NM_001429.3 K1426K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr22:41569697 G>C maps to NM_001429.3 L1563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr22:41551099 C>T maps to NM_001429.3 Q1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr22:41574215 G>A maps to NM_001429.3 Q2167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr22:41545869 C>T maps to NM_001429.3 Q829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr22:41521960 C>T maps to NM_001429.3 Q275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr22:41551099 C>T maps to NM_001429.3 Q1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr22:41553349 G>T maps to NM_001429.3 E1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr22:41531854 C>T maps to NM_001429.3 Q523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr22:41574075 C>T maps to NM_001429.3 Q2121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr22:41553244 C>T maps to NM_001429.3 Q1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr22:41568616 G>T maps to NM_001429.3 E1523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr22:41536228 G>T maps to NM_001429.3 E616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr22:41537114 C>T maps to NM_001429.3 R648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr22:41551099 C>T maps to NM_001429.3 Q1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:132490705 C>G maps to ENST00000333577 L1031L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:132502127 C>T maps to ENST00000333577 I1360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:132522553 G>A maps to ENST00000333577 P2076P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:132502202 G>A maps to ENST00000333577 A1385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:132475179 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:132539677 C>T maps to ENST00000333577 I2639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr12:132547110 G>A maps to ENST00000333577 Q2769Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr12:132547113 G>A maps to ENST00000333577 Q2770Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr12:132547116 G>A maps to ENST00000333577 Q2771Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr12:132547134 G>A maps to ENST00000333577 Q2777Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr12:132547065 C>G maps to ENST00000333577 L2754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr12:132466882 C>T maps to ENST00000333577 Q633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:132547110 G>A maps to ENST00000333577 Q2769Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:132547116 G>A maps to ENST00000333577 Q2771Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:132547119 G>A maps to ENST00000333577 Q2772Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:132497606 C>T maps to ENST00000333577 F1201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr12:132472264 C>T maps to ENST00000333577 Q783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr12:132491246 C>A maps to ENST00000333577 V1079V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr2:46611756 G>A maps to NM_001430.4 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:46609642 C>T maps to NM_001430.4 I789I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr2:46583347 G>A maps to NM_001430.4 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr2:46583933 G>C maps to NM_001430.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:46583939 C>G maps to NM_001430.4 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr2:46588115 C>T maps to NM_001430.4 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:29438878 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:29379625 C>A maps to NM_001166005.1 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:29359652 C>T maps to NM_001166005.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:29391519 C>T maps to NM_001166005.1 I678I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr20:34782185 C>T maps to NM_012156.2 D451D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr20:34770227 C>T maps to NM_012156.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr20:34807702 C>T maps to NM_012156.2 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:34776318 C>T maps to NM_012156.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:34785869 C>T maps to NM_012156.2 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr20:34807737 C>G maps to NM_012156.2 S804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr20:34773197 C>T maps to NM_012156.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr6:131216208 G>C maps to NM_001431.3 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr6:131206306 G>A maps to NM_001431.3 Q588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr6:131190960 C>T maps to NM_001431.3 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr6:131220669 C>T maps to NM_001431.3 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr6:131277439 C>T maps to NM_001431.3 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:131191266 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr6:131277155 G>T maps to NM_001431.3 S157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr18:5397425 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr18:5398075 G>A maps to NM_012307.2 R806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr18:5489113 C>A maps to NM_012307.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr18:5478389 G>A maps to NM_012307.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr5:111504514 G>C maps to NM_022140.3 S618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:111519794 G>A maps to NM_022140.3 Q514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr5:111576459 G>T maps to NM_022140.3 C281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr5:111570402 G>T maps to NM_022140.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr9:111970251 A>G maps to NM_019114.3 C610C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr9:112042114 G>A maps to NM_019114.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr9:112020458 G>A maps to NM_019114.3 C250C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr15:43498759 G>A maps to NM_000119.2 N492N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:21926965 C>T maps to ENST00000265800 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:149519349 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr7:37960489 C>T maps to NM_017549.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr7:37989949 G>A maps to NM_017549.3 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr4:75178019 C>T maps to ENST00000413830 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr7:143090896 G>A maps to NM_005232.4 L855L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr7:143095509 C>T maps to NM_005232.4 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr7:143095482 C>T maps to NM_005232.4 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr7:143098437 G>C maps to NM_005232.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr7:143095497 C>T maps to NM_005232.4 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr7:143095085 G>A maps to NM_005232.4 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:38197143 C>T maps to NM_001099439.1 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:38197173 G>A maps to NM_001099439.1 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:38185673 G>A maps to NM_001099439.1 F823F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:38192826 G>A maps to NM_001099439.1 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:38227611 C>T maps to NM_001099439.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr1:38227179 G>T maps to NM_001099439.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr1:16475401 G>A maps to NM_004431.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr1:16461534 C>T maps to NM_004431.3 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr1:16460020 C>A maps to NM_004431.3 E607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr1:16460033 C>T maps to NM_004431.3 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:16462251 C>T maps to NM_004431.3 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr1:16459783 C>A maps to NM_004431.3 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr1:16456899 G>T maps to NM_004431.3 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:16459809 C>A maps to NM_004431.3 E640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr1:16477415 C>T maps to NM_004431.3 W43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:89259449 C>G maps to NM_005233.5 Y198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr3:89456491 C>G maps to NM_005233.5 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr3:89259356 G>A maps to NM_005233.5 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr3:89480499 T>C maps to NM_005233.5 Y779Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr3:89259371 T>A maps to NM_005233.5 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr3:89259299 T>C maps to NM_005233.5 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr3:89499461 C>T maps to NM_005233.5 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr3:89445005 G>A maps to NM_005233.5 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr2:222298866 G>A maps to NM_004438.3 Q831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr2:222347093 G>A maps to NM_004438.3 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr4:66230765 G>A maps to NM_004439.5 N735N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr4:66467437 G>A maps to NM_004439.5 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:66231706 C>A maps to NM_004439.5 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr4:66356359 C>A maps to NM_004439.5 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr4:66230733 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr4:66231718 G>A maps to NM_004439.5 Q661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr4:66217175 C>T maps to NM_004439.5 V813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr4:66201675 C>T maps to NM_004439.5 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr4:66270150 C>A maps to NM_004439.5 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:96706688 T>C maps to NM_001080448.2 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr3:97311454 G>T did not map to a codon.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr3:97185301 G>T maps to ENST00000514100 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr3:97466365 C>T maps to NM_001080448.2 F1076F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-UY-A78K-01A-11D-A339-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:94068096 G>A maps to NM_004440.3 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:93969198 T>A did not map to a codon.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr6:93955098 T>C maps to NM_004440.3 Q933Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr6:93982042 T>G maps to NM_004440.3 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:94129049 G>A maps to NM_004440.3 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr1:22919900 G>A maps to NM_020526.3 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:22924701 G>C maps to NM_020526.3 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:22927527 C>T maps to NM_020526.3 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr1:22927831 C>T maps to NM_020526.3 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr1:22902807 G>A maps to NM_020526.3 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:22924262 G>A maps to NM_020526.3 E675E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr3:134670622 G>A maps to NM_004441.4 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:134967279 G>A maps to NM_004441.4 E873E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:134920359 C>G maps to NM_004441.4 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr3:134670664 C>T maps to NM_004441.4 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:23233201 G>C did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:23111207 G>A maps to ENST00000400191 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:23189567 G>T maps to ENST00000400191 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:23233233 G>C maps to ENST00000400191 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr3:184295483 C>T maps to NM_004443.3 N506N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:184299391 G>A maps to NM_004443.3 T993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr3:184298212 C>T maps to NM_004443.3 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr3:184290926 C>T maps to NM_004443.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr3:184290794 G>A maps to NM_004443.3 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr7:100410819 G>A maps to NM_004444.4 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:142566062 T>C maps to NM_004445.3 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr7:142568643 C>A maps to NM_004445.3 S1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr7:142568016 T>C maps to NM_004445.3 C886C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr1:226026376 C>T maps to NM_001136018.2 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:226030076 G>A maps to NM_001136018.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:27361251 C>T maps to ENST00000458037 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr8:27358514 C>A maps to ENST00000458037 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr8:27364480 G>A maps to ENST00000458037 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr8:27401984 C>G maps to ENST00000458037 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr19:15341818 G>T maps to NM_001142886.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr19:15338268 G>A maps to NM_001142886.1 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr19:15338451 C>T maps to NM_001142886.1 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr1:92511152 C>T maps to NM_173567.4 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:92515896 C>T maps to NM_173567.4 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr6:145956522 G>A maps to NM_005670.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:37033277 G>A maps to NM_014805.3 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:37033450 G>C maps to NM_014805.3 S373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr19:56200275 G>A maps to NM_001130071.1 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr19:56204329 C>T maps to NM_001130071.1 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:56190130 C>G maps to NM_001130071.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr19:56206595 C>G maps to NM_001130071.1 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr19:56206574 C>T maps to NM_001130071.1 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:19215375 C>T maps to NM_014964.4 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:48614132 G>A maps to NM_017957.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:48618873 G>A maps to NM_017957.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:100320677 C>G maps to NM_000799.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr7:100320698 C>T maps to NM_000799.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:11493834 G>A maps to NM_000121.3 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr19:11489166 C>T maps to NM_000121.3 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr8:144942234 G>A maps to NM_031308.1 F1729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr8:144942387 G>A maps to NM_031308.1 I1678I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:144943482 C>G maps to NM_031308.1 L1313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr8:144946755 G>A maps to NM_031308.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:144940698 C>T maps to NM_031308.1 E2241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:144947097 C>T maps to NM_031308.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:144940860 G>A maps to NM_031308.1 L2187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr8:144942582 G>A maps to NM_031308.1 F1613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr8:144943014 G>C maps to NM_031308.1 L1469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr8:144940773 G>A maps to NM_031308.1 V2216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr8:144940653 G>A maps to NM_031308.1 P2256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr8:144940344 C>T maps to NM_031308.1 V2359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr8:144945879 G>A maps to NM_031308.1 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr8:144941424 C>T maps to NM_031308.1 E1999E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:220162080 G>A maps to NM_004446.2 Q876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:220208270 C>T maps to NM_004446.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr1:220142228 G>A maps to NM_004446.2 L1486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:220174522 G>T maps to NM_004446.2 S713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:51929377 G>A maps to NM_001981.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:51934201 C>T maps to NM_001981.2 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr1:51869161 C>A maps to NM_001981.2 E574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr1:51912717 T>C maps to NM_001981.2 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:16535905 G>A maps to ENST00000455140 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:16532170 G>A maps to ENST00000455140 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:16495954 G>A maps to ENST00000455140 F744F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:16528406 C>T maps to ENST00000455140 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr19:16532278 C>T maps to ENST00000455140 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr12:15803920 G>A maps to NM_004447.5 Q424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr12:15803940 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr12:15815013 A>G maps to NM_004447.5 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:15818801 A>G maps to NM_004447.5 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:15803791 G>A maps to NM_004447.5 Q467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr12:15822337 G>A maps to NM_004447.5 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr12:15822383 C>T maps to NM_004447.5 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr12:15822601 G>C maps to NM_004447.5 S121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr12:15807189 G>T maps to NM_004447.5 S380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:15807105 G>T maps to NM_004447.5 S408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:15823803 G>A maps to NM_004447.5 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr19:55598800 G>T maps to NM_133180.2 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:55594760 G>A maps to NM_133180.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr19:55597505 G>A maps to NM_133180.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr11:721617 G>A maps to NM_022772.3 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:720213 C>T maps to NM_022772.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:721668 G>A maps to NM_022772.3 K291K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr11:721617 G>A maps to NM_022772.3 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:110301958 C>T maps to NM_139053.1 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr1:110301280 G>A maps to NM_139053.1 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr1:110294320 G>A maps to NM_139053.1 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr1:110301185 C>T maps to NM_139053.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr2:26609374 C>T maps to NM_033505.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:91366757 C>G did not map to a codon.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr17:27187543 C>T maps to NM_005702.2 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:27186106 G>A maps to NM_005702.2 Q362Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr17:27185604 G>A maps to NM_005702.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr5:96132898 C>T maps to NM_016442.3 K259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr5:96136616 G>C maps to NM_016442.3 S204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr5:96139221 G>A maps to NM_016442.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr5:96249153 C>T maps to NM_001130140.1 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr5:96215595 C>T maps to NM_001130140.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr5:96244712 C>G maps to NM_001130140.1 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr5:96244817 C>A maps to NM_001130140.1 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr23:48687713 C>G did not map to a codon.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr23:48687773 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:37884047 C>G maps to NM_004448.2 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:37884179 C>T maps to NM_004448.2 F1217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:37879819 G>A maps to NM_004448.2 A705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr17:37872106 C>T maps to NM_004448.2 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr17:37872617 C>G maps to NM_004448.2 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr17:37866351 C>A maps to NM_004448.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr17:37868199 C>T maps to NM_004448.2 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:37883948 G>A maps to NM_004448.2 V1140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:37881040 G>A maps to NM_004448.2 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:37865655 G>A maps to NM_004448.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr17:37868681 C>T maps to NM_004448.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr17:37881978 G>C maps to NM_004448.2 L915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr17:37864602 C>G maps to NM_004448.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr17:37864713 G>A maps to NM_004448.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:37871730 C>T maps to NM_004448.2 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:65349977 C>T maps to ENST00000506030 F944F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr5:65372199 C>T maps to ENST00000506030 V1347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr12:56480393 G>C maps to NM_001982.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr12:56491633 C>G maps to NM_001982.2 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:56492570 C>T maps to NM_001982.2 F907F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:56495808 T>C maps to NM_001982.2 L1333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:56477580 G>A maps to NM_001982.2 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:56490339 C>A maps to NM_001982.2 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr12:56492345 T>C maps to NM_001982.2 D893D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr12:56495057 C>T maps to NM_001982.2 L1139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:212530178 G>T maps to NM_005235.2 C580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr2:212522498 G>A maps to NM_005235.2 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr2:212522504 G>T maps to NM_005235.2 G640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:212288889 G>A maps to NM_005235.2 V952V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr12:1292586 G>A maps to NM_178040.2 K719K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr12:1291201 C>T maps to NM_178040.2 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr12:1219411 C>T maps to NM_178040.2 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:56468429 C>T maps to ENST00000460849 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr3:56026124 C>A maps to ENST00000460849 E739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:56026146 C>T maps to ENST00000460849 E731E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:45920134 G>C maps to NM_202001.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr19:45868142 G>A maps to NM_000400.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr19:45856033 G>C maps to NM_000400.3 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:45860916 C>G maps to NM_000400.3 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr2:128036774 T>C maps to NM_000122.1 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:128016991 T>C maps to NM_000122.1 E699E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:128015225 C>T maps to NM_000122.1 R765R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:128051121 C>T maps to NM_000122.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr2:128029014 C>T maps to NM_000122.1 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr2:128036837 C>G maps to NM_000122.1 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr16:14042114 C>T maps to NM_005236.2 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:103515211 G>A maps to NM_000123.2 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:50678884 G>A maps to NM_000124.2 Q1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr10:50740775 G>A maps to ENST00000515869 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr10:50708621 C>G maps to NM_000124.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr10:50732713 C>T maps to ENST00000515869 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:71427163 A>T did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr23:71426403 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr23:71427802 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:71427660 G>T did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:71426415 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:71428440 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:71427454 C>G did not map to a codon.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr5:60186871 C>T maps to NM_000082.3 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:75250496 C>G maps to NM_001432.2 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr4:75248367 A>G maps to NM_001432.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr19:42752673 C>A maps to NM_006494.2 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr19:42752823 G>C maps to NM_006494.2 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:42753747 G>A maps to NM_006494.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr21:39947588 G>A maps to NM_001136154.1 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr5:172359484 T>G maps to NM_001031711.2 Y196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr12:29498395 G>A maps to NM_016570.2 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr12:29523099 T>C maps to NM_016570.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr12:29523095 G>A maps to NM_016570.2 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr12:29496107 G>A maps to NM_016570.2 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr20:34145205 C>G maps to ENST00000447986 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr8:8887447 C>T maps to NM_153332.3 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr16:20811623 C>T maps to NM_001142725.1 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr16:20811724 C>G did not map to a codon.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr8:618596 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr8:623492 C>A maps to NM_207332.1 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:54028616 G>A maps to NM_015701.3 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:54036355 C>T maps to NM_015701.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr2:54028960 T>C maps to NM_015701.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr2:54028966 G>A maps to NM_015701.3 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr10:101943527 C>A maps to NM_001100626.1 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr1:43308815 G>A maps to NM_018538.3 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr1:43308794 G>A maps to NM_018538.3 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr2:158182009 G>A maps to NM_001009959.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr9:5810172 G>A maps to NM_024896.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr9:5830742 T>C maps to NM_024896.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr16:23702713 C>T maps to NM_033266.3 E851E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr16:23706102 G>C maps to NM_033266.3 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr16:23706108 G>A maps to NM_033266.3 I728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr16:23724592 C>T maps to NM_033266.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr16:23713553 C>A maps to NM_033266.3 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:23716427 G>A maps to NM_033266.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:23724502 C>T maps to NM_033266.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:23713553 C>T maps to NM_033266.3 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr16:23722242 G>A maps to NM_033266.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:23706376 C>T maps to NM_033266.3 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr14:53119988 G>A maps to NM_014584.1 Q285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:236393547 C>A maps to NM_019891.3 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:236389642 G>A maps to NM_019891.3 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:15068614 G>A maps to NM_152321.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:15073906 C>A maps to NM_152321.2 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:8074238 G>A maps to NM_018948.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr7:64452732 G>C maps to NM_001007253.3 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:124623757 G>A maps to NM_138961.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr18:19154690 T>C maps to NM_052911.2 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr18:19154592 G>C maps to NM_052911.2 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr20:13695733 C>T maps to NM_016649.3 K781K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr12:53662887 G>A maps to NM_012291.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr12:53670541 G>A maps to NM_012291.4 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr12:53687249 C>T maps to NM_012291.4 L2119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr12:53668711 G>T maps to NM_012291.4 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr12:53676184 C>G maps to NM_012291.4 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr12:53673529 G>A maps to NM_012291.4 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr12:53685628 C>G maps to NM_012291.4 V1892V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr12:53670983 C>T maps to NM_012291.4 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:53668686 G>T maps to NM_012291.4 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr12:53663770 C>T maps to NM_012291.4 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr12:53682465 C>G maps to NM_012291.4 S1564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:6505988 G>A maps to NM_031475.2 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:6488464 C>G maps to NM_031475.2 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr1:6511675 C>T maps to NM_031475.2 F643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr6:152382164 C>T maps to NM_001122741.1 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr14:64701803 C>G maps to NM_001437.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr14:64727308 G>A maps to NM_001437.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr14:64701716 C>T maps to NM_001437.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr8:95674783 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:95653663 C>T maps to NM_017697.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr8:95680447 C>G maps to NM_017697.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr8:95653663 C>T maps to NM_017697.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr8:95690515 G>A maps to NM_017697.3 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr16:68269813 C>G maps to NM_024939.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:64082559 C>G maps to NM_004451.3 S277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr14:76964692 G>A maps to NM_004452.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr14:76928978 C>A maps to NM_004452.3 C163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr14:76964701 G>A maps to NM_004452.3 Q401Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:216692577 G>A maps to NM_001438.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr1:216737706 G>C maps to NM_001438.2 S239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:216850700 G>A maps to NM_001438.2 D63D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:216850552 G>A maps to NM_001438.2 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr23:103499059 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr23:103499469 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:103499165 T>G did not map to a codon.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr23:103494919 G>C did not map to a codon.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr23:103498919 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:103495518 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr23:103495475 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr12:56531824 C>A maps to NM_001184796.1 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr12:56536836 C>G maps to NM_001184796.1 P1018P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:56536447 C>T maps to NM_001184796.1 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:56531078 G>A maps to NM_001184796.1 E630E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr12:56532788 G>T maps to NM_001184796.1 E872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr12:56528163 G>A maps to NM_001184796.1 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr12:56526286 C>G maps to NM_001184796.1 S356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr12:56525268 C>T maps to NM_001184796.1 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr7:158528299 C>T did not map to a codon.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr7:158560362 C>T maps to NM_020728.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr7:158534302 T>A maps to NM_020728.2 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr7:158540923 G>A maps to NM_020728.2 F562F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:158560446 G>A maps to NM_020728.2 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:138174085 C>T maps to NM_031913.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:138195289 G>A maps to NM_031913.3 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:138187707 C>T maps to NM_031913.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:67630884 G>A maps to NM_019002.3 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:67632390 C>T maps to NM_019002.3 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr5:137846292 T>A maps to NM_004730.2 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr19:51857427 G>A maps to NM_001014763.1 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr19:51853642 G>A maps to NM_001014763.1 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:51857658 G>A maps to NM_001014763.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:51856529 G>A maps to NM_001014763.1 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:22797220 C>T maps to NM_001039481.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr12:22826479 G>A maps to NM_018638.4 Q366Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr1:204106291 C>T maps to NM_018208.2 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:204106258 G>C maps to NM_018208.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr21:40191550 G>A maps to NM_005239.4 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:40191556 C>T maps to NM_005239.4 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr21:40194792 C>T maps to NM_005239.4 Q464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr7:13978871 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:13949260 G>A maps to NM_004956.4 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr7:13978848 C>T maps to NM_004956.4 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr7:13978872 T>A did not map to a codon.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr7:13946144 A>G maps to NM_004956.4 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr7:13940452 A>G maps to NM_004956.4 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:41606895 C>T maps to NM_001079675.1 E368E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:41610075 G>A maps to NM_001079675.1 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr17:41622707 C>A maps to NM_001079675.1 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr17:41622708 G>T maps to NM_001079675.1 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:41606502 C>T maps to NM_001079675.1 K410K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:41622349 G>A maps to NM_001079675.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr3:185766490 G>A maps to NM_004454.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr3:185798860 A>G maps to NM_004454.2 Y112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr3:185797612 C>A maps to NM_004454.2 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:12037407 C>T maps to NM_001987.4 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:12022356 G>T did not map to a codon.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr12:12006394 G>T maps to NM_001987.4 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:12043946 G>A maps to NM_001987.4 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr12:12022562 G>A maps to NM_001987.4 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr6:36336704 C>A did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr6:36343649 G>C maps to NM_016135.2 S102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr6:36343675 G>A maps to NM_016135.2 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:5733342 C>T maps to NM_153717.2 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr4:5624325 G>A maps to NM_147127.4 D813D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr4:5564655 C>T maps to NM_147127.4 E1282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr17:29645897 G>C maps to NM_001003927.2 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:29632418 G>C maps to NM_006495.3 S70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr17:29632165 C>T maps to NM_006495.3 Q154Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr1:93101857 C>T maps to NM_005665.4 V460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr19:7927311 G>A maps to NM_001159944.1 A613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:74005808 G>A maps to NM_001988.2 L1159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr17:74003231 G>A maps to NM_001988.2 Y2018Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr17:74015619 G>A maps to NM_001988.2 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr17:74004085 C>A maps to NM_001988.2 E1734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:74003726 G>A maps to NM_001988.2 I1853I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr17:74011019 G>A maps to NM_001988.2 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr17:74005730 C>T maps to NM_001988.2 K1185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr17:74019585 C>T maps to NM_001988.2 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr17:74006000 C>G maps to NM_001988.2 L1095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr17:74004161 G>A maps to NM_001988.2 I1708I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr17:74004347 G>A maps to NM_001988.2 L1646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr7:27285923 G>A maps to NM_001989.3 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:176947096 C>A maps to NM_001080458.1 G170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr22:29669815 G>A maps to NM_013986.3 Q63Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:140262392 C>A maps to NM_017820.3 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr9:140250820 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:242048725 G>A maps to NM_006027.4 Q774Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr1:242042604 C>G maps to NM_006027.4 S690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:242023907 C>T maps to NM_006027.4 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr1:242042338 T>A maps to NM_006027.4 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:56737392 C>T maps to NM_018261.3 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr4:56757479 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:599130 T>C maps to NM_018303.4 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:592472 C>T maps to NM_018303.4 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr6:532571 G>C maps to NM_018303.4 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr6:617744 G>C maps to NM_018303.4 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr6:592508 G>C maps to NM_018303.4 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr6:617831 A>G maps to NM_018303.4 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:617744 G>A maps to NM_018303.4 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr5:458067 G>A maps to ENST00000315013 W416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr5:462320 G>T maps to ENST00000315013 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr5:453800 T>A maps to ENST00000315013 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr5:464427 G>A maps to ENST00000315013 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr5:464493 C>T maps to ENST00000315013 N591N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr5:454014 C>T maps to ENST00000315013 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr16:67218810 G>A maps to NM_178516.3 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:132990734 C>T maps to NM_021807.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:132937918 C>A maps to NM_021807.3 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:132937898 C>T maps to NM_021807.3 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:132990734 C>G maps to NM_021807.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:57711055 C>A maps to ENST00000340918 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr14:57689134 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr10:94733955 G>A maps to NM_019053.4 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr10:94688172 G>A maps to NM_019053.4 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr2:72802652 G>A maps to NM_015189.1 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr2:72968483 C>T maps to NM_015189.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr2:72722560 T>C maps to NM_015189.1 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr17:74080124 C>T maps to NM_001145297.2 K689K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:74093985 G>A maps to NM_001145297.2 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:74081810 C>G maps to NM_001145297.2 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:231472147 G>A maps to NM_175876.3 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:231471481 C>T maps to NM_175876.3 K670K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr3:38565703 C>T maps to NM_005107.3 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:38565819 G>A maps to NM_005107.3 E358E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr10:99205530 C>A maps to NM_016046.3 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr10:99205548 G>A maps to NM_016046.3 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr1:11148179 C>T maps to NM_001001998.1 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr1:11147609 C>G maps to NM_001001998.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr1:11159776 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:11132176 C>A maps to NM_001001998.1 E737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr1:11136910 G>A maps to NM_001001998.1 I658I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr1:11137482 G>A maps to NM_001001998.1 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr8:145134874 G>A maps to NM_019037.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr8:145135365 G>A maps to NM_019037.2 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr13:37580264 C>T maps to NM_181503.2 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr4:122723855 T>G maps to NM_001034194.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr11:108382970 G>C maps to NM_015065.2 S1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr11:108412451 G>A maps to NM_015065.2 C69C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr11:108409777 G>C maps to NM_015065.2 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:108464257 C>T maps to NM_015065.2 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr11:108384052 G>C maps to NM_015065.2 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr11:108381113 G>C maps to NM_015065.2 S1707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr8:119122780 G>A maps to NM_000127.2 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:118847772 C>T maps to NM_000127.2 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr8:119122832 C>A maps to NM_000127.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr8:119122469 C>A maps to NM_000127.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr8:119122826 G>C maps to NM_000127.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr8:118812030 G>A maps to NM_000127.2 Q721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr11:44135764 G>C maps to NM_000401.3 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr11:44228469 C>T maps to NM_000401.3 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:44129412 G>T maps to NM_000401.3 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr11:44146518 C>G maps to NM_000401.3 Y341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:44255774 G>T maps to NM_000401.3 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr1:26349271 C>T maps to NM_004455.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr8:72123471 C>T maps to NM_000503.4 E539E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr8:72246339 G>C maps to NM_000503.4 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr8:72211938 T>A maps to NM_000503.4 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr8:72234076 G>A maps to NM_000503.4 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr8:72127943 C>T maps to NM_000503.4 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr20:45633579 G>C did not map to a codon.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr20:45630088 G>A maps to ENST00000360649 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr20:45797817 C>G maps to ENST00000360649 S342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr20:45618708 G>A maps to ENST00000360649 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:28365385 G>T maps to NM_001990.2 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:28320056 G>C maps to NM_001990.2 S386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr1:28362170 G>C maps to NM_001990.2 S82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr6:133827305 T>C maps to ENST00000452339 D424D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr6:133836457 G>A did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr6:133849924 G>A maps to ENST00000452339 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr6:133769306 T>A maps to ENST00000452339 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:133802664 G>A maps to ENST00000452339 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr6:66204880 C>T maps to ENST00000370616 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:40874831 C>T maps to ENST00000264646 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:40864324 C>A maps to ENST00000264646 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:40855799 G>A maps to ENST00000264646 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:40876418 C>G maps to ENST00000264646 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:40874882 C>G maps to ENST00000264646 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr17:40870490 T>C maps to ENST00000264646 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:148512131 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:148514355 G>A maps to NM_004456.3 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr7:148511212 C>A maps to NM_004456.3 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:148526868 G>A maps to NM_004456.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr7:148523597 G>A maps to NM_004456.3 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr7:148529803 G>A maps to NM_004456.3 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:159204663 G>A maps to NM_001111077.1 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr6:159205677 G>A maps to NM_001111077.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr6:159206348 G>A maps to NM_001111077.1 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr6:159188082 G>A maps to NM_001111077.1 R542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr13:113803476 C>A maps to NM_000504.3 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr13:113803350 G>A maps to NM_000504.3 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr13:113783853 C>T maps to NM_000504.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:176831014 C>T maps to NM_000505.3 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr5:176830945 G>A maps to NM_000505.3 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr5:176831564 G>A maps to NM_000505.3 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr5:176831359 C>T maps to NM_000505.3 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr5:176831245 C>G maps to NM_000505.3 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr5:176831362 C>T maps to NM_000505.3 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr5:176829574 G>A maps to NM_000505.3 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:6152169 G>A maps to NM_000129.3 Q641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr6:6182375 T>C did not map to a codon.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr6:6318795 G>T maps to NM_000129.3 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr6:6145932 C>A maps to NM_000129.3 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:197024860 G>C maps to NM_001994.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr1:197026565 G>A maps to NM_001994.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr1:197029555 C>A maps to NM_001994.2 G249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr1:197032026 C>T maps to NM_001994.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:197032043 G>A maps to NM_001994.2 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr1:197031987 G>A maps to NM_001994.2 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:46749599 C>T maps to NM_000506.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr11:46750321 G>A maps to NM_000506.3 K469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr11:46742352 G>A maps to NM_000506.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:76029316 C>T maps to NM_001992.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr5:76029018 C>T maps to NM_001992.3 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr5:76028928 C>A maps to NM_001992.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr5:76129502 C>T maps to NM_005242.4 N357N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr5:75914342 C>T maps to NM_004101.2 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr5:75913508 G>T maps to NM_004101.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:17000939 C>T maps to NM_003950.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr19:17000711 G>A maps to NM_003950.2 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:17001212 C>T maps to NM_003950.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr1:94997898 G>T maps to NM_001993.4 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:169494147 T>C did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:169511936 G>C maps to ENST00000367796 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:169519104 G>A maps to ENST00000367796 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:169483550 C>A maps to ENST00000367796 *2230Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:169510460 G>A maps to ENST00000367796 F1294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:169511528 G>T maps to ENST00000367796 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:169498882 G>A maps to ENST00000367796 L1799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:169510772 G>C maps to ENST00000367796 V1190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:169494093 G>A maps to ENST00000367796 I1928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr1:169513702 G>A maps to ENST00000367796 F607F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:154158230 A>G did not map to a codon.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr23:154124397 C>G did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:154157863 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr23:154197728 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr23:154194884 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:154088778 C>T did not map to a codon.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr23:154194914 G>T did not map to a codon.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr23:154157893 C>A did not map to a codon.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr23:154090122 C>A did not map to a codon.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr23:154091364 A>T did not map to a codon.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr23:154156855 G>C did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:154221359 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:154197619 G>C did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr23:154227804 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:154225343 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:154158594 A>G did not map to a codon.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr23:154157346 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:154157099 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:154227851 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:154159708 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:154159889 C>A did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:154124390 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:154132252 G>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr23:154133154 T>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr23:154157719 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr23:154176072 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr23:154157486 A>G did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr23:138644014 T>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:138619284 T>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr23:138643821 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr23:138612940 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr16:74750317 C>T maps to NM_024306.4 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr1:46877298 C>G maps to NM_001441.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr23:57313382 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:57515265 C>G did not map to a codon.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr2:88425823 C>A maps to NM_001443.1 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr2:88425769 C>G maps to NM_001443.1 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr8:82439284 C>T maps to NM_001105281.1 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr5:159640783 G>A maps to NM_001040442.1 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr11:70052281 A>G maps to NM_003824.3 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:70049612 G>A maps to NM_003824.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr11:70052577 G>C maps to NM_003824.3 *209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:61570833 C>T did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:61580783 C>T maps to NM_013402.4 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:61570385 C>T maps to NM_013402.4 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:61644426 G>C maps to NM_021727.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:61643327 G>A maps to NM_021727.3 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:61645630 G>A maps to NM_021727.3 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr11:61647623 C>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr11:61645633 G>A maps to NM_021727.3 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr11:61646007 G>A maps to NM_021727.3 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr17:72888658 G>A maps to ENST00000310226 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:50941243 C>T maps to NM_007051.2 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:51005270 C>T maps to NM_007051.2 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:50956337 C>G did not map to a codon.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr1:51005321 C>A maps to NM_007051.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:51050453 A>G maps to NM_007051.2 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:80465455 C>T maps to NM_000137.1 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr15:80465389 C>T maps to NM_000137.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr15:80467380 G>T maps to NM_000137.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:1877385 C>T maps to NM_001018104.2 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:96072878 G>T maps to NM_016044.2 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:97751471 G>A maps to NM_199336.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr12:50283284 G>A maps to NM_012306.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:207087416 G>A maps to NM_005449.4 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr16:4664714 C>A maps to NM_145253.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr12:124798908 C>G maps to ENST00000389727 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr9:130742368 G>A maps to NM_001035254.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:130710380 G>A maps to NM_001035254.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:109103118 C>T maps to NM_001010883.2 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr1:109143229 C>T maps to NM_001010883.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:55172593 G>A did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr23:55185597 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr23:55172571 G>A did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr5:14602365 C>G maps to NM_019018.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr5:14609092 G>C maps to NM_019018.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:14602290 G>T did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr5:14602374 G>T maps to NM_019018.2 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr5:14601152 G>A maps to NM_019018.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr5:14678823 C>T maps to NM_138348.4 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr5:14693129 C>T maps to NM_138348.4 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr10:14816389 C>T maps to NM_031453.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr19:1881472 C>T maps to NM_031213.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr9:74489885 C>T maps to NM_016014.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr20:825767 C>T maps to NM_031424.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr8:59058878 G>C maps to NM_147189.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr8:59059538 C>T maps to NM_147189.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:45599 C>T maps to NM_001077710.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr2:46088 C>T maps to NM_001077710.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr11:58920184 A>G maps to NM_198847.2 K348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr11:58920670 G>A maps to NM_198847.2 E510E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr11:58920550 T>C maps to NM_198847.2 H470H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr11:58893254 G>A maps to NM_198947.3 W562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:58893518 C>G maps to NM_198947.3 S650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:58892922 C>T maps to NM_198947.3 C451C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr11:58892341 G>T maps to NM_198947.3 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr11:58893357 C>T maps to NM_198947.3 N596N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr20:2819521 C>G maps to NM_022760.3 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr20:2819392 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:38910247 G>A maps to NM_138389.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:153381911 C>G maps to ENST00000442256 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr3:57658152 G>A maps to NM_152678.2 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr22:50753331 C>G maps to NM_001001794.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr2:203630258 C>A maps to NM_173511.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr2:203630477 T>C maps to NM_173511.3 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr2:203590971 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr2:203589704 T>C maps to NM_173511.3 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr22:45726590 C>T maps to NM_017911.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr22:45719181 C>T maps to NM_017911.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr9:96305553 C>T maps to ENST00000333936 Q682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr9:96320267 C>T maps to ENST00000333936 Q910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:96233608 G>T maps to ENST00000333936 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr9:96233449 C>T maps to ENST00000333936 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr9:96259827 C>T maps to ENST00000333936 Q294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr9:96318704 C>T maps to ENST00000333936 L800L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-GC-A3RB-01A-12D-A21Z-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr9:96214619 C>G maps to ENST00000333936 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr9:96233437 G>T maps to ENST00000333936 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr9:96318697 C>G maps to ENST00000333936 S798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr9:96212867 C>A maps to NM_198841.2 G193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr23:54114293 C>A did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr23:54143002 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr23:54162952 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr23:54185804 A>G did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr23:54185902 C>G did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr23:54143100 T>A did not map to a codon.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr23:54186018 C>T did not map to a codon.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr23:54159250 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:54114377 C>T did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr9:71395442 C>T maps to NM_138333.3 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:133915912 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr23:133979244 T>C did not map to a codon.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr23:133963289 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:133941726 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:133988221 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr13:25744248 C>T maps to NM_152704.2 K503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr23:63411795 C>G did not map to a codon.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr23:63413138 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr23:63410226 C>A did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr23:63411968 C>A did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr23:63412289 C>T did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr23:63412574 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:63412574 C>T did not map to a codon.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr23:63412025 C>T did not map to a codon.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr23:63410940 C>T did not map to a codon.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr23:63412304 C>T did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:63410906 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:63412529 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:63412010 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr23:63411642 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr23:63410257 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:63411957 A>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:131520310 C>G maps to NM_001105195.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr2:131520439 G>C maps to NM_001105195.1 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr2:131520172 G>A maps to NM_001105195.1 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr13:51826226 C>T maps to NM_145019.2 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr13:51826063 C>T maps to NM_145019.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr13:51855295 C>T maps to NM_145019.2 C551C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr13:51825658 C>T maps to NM_145019.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr2:225265852 C>T maps to NM_001122779.1 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr19:17534561 G>A maps to NM_138401.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr19:17531135 C>G maps to NM_138401.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:129157917 C>T maps to NM_033446.1 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:129148858 T>C maps to NM_033446.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr9:129157881 C>T maps to NM_033446.1 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr9:129157851 A>G did not map to a codon.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr7:22985594 T>C maps to NM_032581.3 E393E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:23004146 G>A maps to NM_032581.3 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr2:201873709 G>A maps to NM_173822.3 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr23:134166412 G>A did not map to a codon.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr23:134166742 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:134166536 G>A did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:134166689 G>A did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr23:134185975 C>T did not map to a codon.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr23:134186000 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr23:134185861 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr23:134156398 C>T did not map to a codon.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr1:184787959 C>T did not map to a codon.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr1:184792382 C>G maps to NM_052966.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr1:184863262 C>T maps to NM_052966.2 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr9:130341207 C>T maps to NM_001035534.1 W3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:17644436 G>A maps to ENST00000335393 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr3:184062487 C>T maps to NM_144635.4 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:143053717 G>C maps to NM_001031690.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr7:143055950 G>A maps to NM_001031690.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr1:1179463 G>C maps to NM_001014980.1 S134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr1:1179863 G>C maps to NM_001014980.1 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr23:92964787 G>A did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr23:92964635 T>A did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr5:16479023 G>C maps to NM_001034850.1 S248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr5:16478158 G>T maps to NM_001034850.1 S286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr5:16475168 G>C maps to NM_001034850.1 S392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:71238129 G>C maps to NM_001162529.1 L1250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr6:71191810 C>T maps to NM_001162529.1 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr6:71185218 C>T maps to NM_001162529.1 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr6:71234833 C>T maps to NM_001162529.1 R683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr6:71269608 C>G maps to NM_001162529.1 L1511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:139278011 C>G maps to NM_015912.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:139144874 C>T maps to NM_015912.3 E1394E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr8:139151322 C>T maps to NM_015912.3 Q1269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr8:139153498 C>A maps to NM_015912.3 L1244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr8:139144999 G>A maps to NM_015912.3 L1353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr8:139153546 G>A maps to NM_015912.3 L1228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr4:89671698 G>A maps to NM_014883.2 Q606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:89702485 C>A maps to NM_014883.2 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr4:89660242 G>A maps to NM_014883.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr5:137278655 C>T maps to NM_016603.2 Q810Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr10:61028375 G>A maps to ENST00000442566 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr4:187078791 C>T maps to ENST00000356371 H507H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr4:187073127 G>A maps to ENST00000356371 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr2:286343 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:55077291 G>A maps to NM_176782.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr5:79797731 G>C maps to NM_205548.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr5:79837647 C>T maps to NM_205548.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr9:18928109 G>A maps to NM_153707.2 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr9:18950935 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr9:18941668 A>G maps to NM_153707.2 C129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:82575105 T>C maps to NM_001008226.1 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:108518059 G>T maps to NM_001080396.2 Y295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr13:108518237 G>T maps to NM_001080396.2 S236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr13:108518491 G>A maps to NM_001080396.2 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr13:107862947 G>T maps to NM_001080396.2 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr23:68725796 G>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:68749657 C>T did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:53122528 G>C maps to NM_001042693.1 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr11:6244845 G>A maps to NM_032127.3 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr11:6243698 G>A maps to NM_032127.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr11:6239788 C>T maps to NM_032127.3 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr11:6243777 G>C maps to NM_032127.3 S362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:116593032 C>T maps to NM_020940.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr10:116602894 C>T maps to NM_020940.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:62081095 G>A maps to ENST00000404929 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:62067208 C>T maps to ENST00000404929 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:62066590 G>T maps to ENST00000404929 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr14:74411203 G>C maps to NM_152445.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr3:122123147 G>A maps to NM_014367.3 Q67Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr21:35757938 G>T maps to NM_058182.4 *59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr9:140139594 G>A maps to NM_001001710.1 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:35563792 G>C maps to NM_001164310.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:11301722 C>T maps to NM_053279.2 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr11:73120685 C>A maps to ENST00000064778 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:131810475 T>C maps to NM_001009993.2 *196W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr2:131812887 G>A maps to NM_001009993.2 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr2:131812911 G>A maps to NM_001009993.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:98984365 C>G maps to NM_182562.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr5:118970105 G>A maps to ENST00000420106 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr10:15326104 C>G did not map to a codon.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr2:187626454 C>T maps to NM_177454.3 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr2:187626803 C>A maps to NM_177454.3 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr2:187615975 G>C maps to NM_177454.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:10235355 G>T maps to NM_199133.2 Y154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr5:10236712 C>T maps to NM_199133.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr5:99871656 C>T maps to NM_198507.1 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr5:99871244 C>A maps to NM_198507.1 S4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr4:84393398 C>T maps to NM_139076.2 K86K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr10:126490427 C>T maps to NM_032182.3 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr10:126505168 C>G maps to NM_032182.3 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr10:126517395 C>A maps to NM_032182.3 S177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:126519947 C>T maps to NM_032182.3 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr10:126523362 C>T maps to NM_032182.3 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:126490442 C>T maps to NM_032182.3 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr10:126518031 C>T maps to NM_032182.3 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr2:75720592 C>T maps to NM_032181.2 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr14:35546419 C>A maps to NM_173607.3 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:222919976 C>T maps to NM_207468.2 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:102703809 G>A maps to NM_001136123.1 G894G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr10:102709861 G>A maps to NM_001136123.1 Q1050Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr2:29274838 C>G maps to NM_199280.2 L980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr14:45432145 G>A maps to ENST00000361462 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr14:45542645 C>G maps to ENST00000361462 S1735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr14:45494994 C>G maps to ENST00000361462 S1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr14:45512887 G>C did not map to a codon.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr14:45431920 C>G maps to ENST00000361462 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr14:45432532 G>A maps to ENST00000361462 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:135418744 G>C maps to NM_205855.3 S167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr14:94395291 C>T maps to NM_138344.3 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:94394795 C>A maps to NM_138344.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:82444564 G>A maps to NM_175885.3 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr6:119297189 G>C maps to NM_024581.4 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr6:119301413 C>T maps to NM_024581.4 T730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr6:119324143 G>A maps to NM_024581.4 Q670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr6:119300684 T>C did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr6:119288117 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr6:119338030 C>A maps to NM_024581.4 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr12:49994063 G>C maps to NM_032130.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr10:15863725 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr7:30891837 G>C maps to NM_032222.2 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:30831103 C>G maps to NM_032222.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:30821704 C>G maps to NM_032222.2 S99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr9:71990747 C>T maps to NM_001127608.1 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:155220581 G>T maps to ENST00000368370 S333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:10911961 G>A maps to NM_001079512.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr4:91230190 C>G maps to NM_001145065.1 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr10:86198372 G>C maps to ENST00000372088 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr16:57206174 C>T maps to NM_024946.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr4:2661731 C>T maps to ENST00000324666 Q275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr4:2664577 G>T maps to ENST00000324666 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr4:2661670 G>A maps to ENST00000324666 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr4:2661736 G>A maps to ENST00000324666 Q276Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr4:2717760 C>T maps to ENST00000324666 L1212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr4:2695595 C>T maps to ENST00000324666 V738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr4:2692425 G>C maps to ENST00000324666 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr4:2659570 G>A maps to ENST00000324666 W160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr4:2691312 G>A maps to ENST00000324666 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr3:150421319 C>T maps to NM_152394.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr23:103411482 C>T did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:103411589 G>C did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr23:103431233 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:103411544 C>A did not map to a codon.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr3:68466475 G>A maps to NM_213609.2 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr12:62148676 G>A maps to NM_178539.3 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr3:68802169 C>T did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr22:48972291 G>A did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr22:48972291 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr22:49103649 C>A maps to ENST00000336769 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:66537026 G>C maps to NM_017565.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr17:66535529 G>A maps to NM_017565.3 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:179019500 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr1:179013135 C>T maps to NM_014864.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr10:51892704 G>C maps to NM_001005751.1 *1342Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr10:51829386 T>C maps to NM_001005751.1 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr10:47909769 C>T maps to NM_018232.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:46261180 C>T maps to ENST00000399588 Q598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr10:88994222 C>T maps to NM_001099338.1 Q799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr9:97082693 C>T maps to NM_017561.1 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:97082699 G>C maps to NM_017561.1 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr9:97083510 G>A maps to NM_017561.1 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr9:97088046 G>C maps to NM_017561.1 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr9:99699433 C>T maps to NM_001170741.1 H357H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr10:88911707 G>C maps to ENST00000298786 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr10:88939919 G>A maps to ENST00000298786 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr18:10671658 C>T maps to NM_022068.2 L2708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr18:10696491 G>A maps to NM_022068.2 L2178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:153741214 C>A did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr7:120991194 A>T did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:58631353 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:58631327 G>A maps to NM_138805.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr1:110586409 C>T maps to NM_033088.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:110592107 G>A maps to NM_033088.2 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:110581903 C>T maps to NM_033088.2 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr1:110587460 G>C did not map to a codon.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr1:110584461 G>A maps to NM_033088.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr1:110581816 C>T maps to NM_033088.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:110593663 G>A maps to NM_033088.2 W681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:129110494 C>G maps to ENST00000450266 S687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:20879525 G>A maps to NM_207334.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr10:120879961 C>G maps to NM_207009.2 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr10:120877093 G>A maps to NM_207009.2 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:82461732 G>A maps to ENST00000369756 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:27332435 C>G maps to NM_052943.3 *426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:79699184 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:79698391 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr23:79698074 C>T did not map to a codon.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr23:34149313 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr23:34149631 C>T did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:34149313 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr23:34148658 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr23:34150088 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr23:34149794 G>A did not map to a codon.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr23:34148721 C>G did not map to a codon.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr23:34148765 G>C did not map to a codon.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr23:34148160 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:34149300 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr23:34150374 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:34148132 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr23:34961454 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr23:34961689 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr23:34961581 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr23:34962423 C>T did not map to a codon.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr23:34961077 G>C did not map to a codon.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr23:34961467 G>A did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr23:34961686 C>G did not map to a codon.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr23:34960987 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:34962541 C>T did not map to a codon.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr23:34961522 C>T did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr23:34961553 G>T did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr23:34961554 C>A did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:34961899 A>T did not map to a codon.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:37028496 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr23:37029099 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr23:37027155 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr23:37027199 A>C did not map to a codon.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:37027544 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:37026773 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr23:37027609 C>A did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr23:37027155 C>G did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr23:37027155 C>G did not map to a codon.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr23:37027783 G>A did not map to a codon.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr23:37027113 C>T did not map to a codon.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr23:37029298 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:37027998 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr23:37027149 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:37027963 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:37029031 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr13:37584736 C>T maps to NM_001014286.2 Q718Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr13:37603940 G>A maps to NM_001014286.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr2:16747024 A>G maps to NM_030797.3 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:16743289 G>A maps to NM_030797.3 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:16743409 C>A did not map to a codon.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr2:16743409 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr2:16734263 G>A maps to NM_030797.3 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:153674217 G>C did not map to a codon.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr23:153673978 A>T did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:3850758 C>T maps to NM_012135.1 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:3850671 G>A maps to NM_012135.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr4:1656881 G>A maps to NM_001174070.1 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr4:1643301 G>A maps to NM_001174070.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr4:1643172 G>A maps to NM_001174070.1 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr10:126370703 G>A maps to NM_014661.3 C126C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr10:126370734 G>T maps to NM_014661.3 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:26153216 G>A maps to NM_001099626.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:26153135 G>A maps to NM_001099626.1 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr1:26153141 C>T maps to NM_001099626.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:26158515 G>A maps to NM_001099626.1 *293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr11:114393094 C>G maps to ENST00000424269 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr11:114569242 C>T maps to NM_182495.5 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:101540510 C>T maps to NM_145037.2 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:101540530 C>T maps to NM_145037.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr17:643743 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:30037952 G>A maps to NM_031478.4 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr16:30038106 G>A maps to NM_031478.4 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr23:152858022 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr23:152858158 G>T did not map to a codon.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr18:30050349 C>T maps to ENST00000269209 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr18:29848661 C>A maps to ENST00000269209 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr18:29867521 C>T maps to ENST00000269209 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr18:29867275 A>G maps to ENST00000269209 D428D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr18:29867338 C>T maps to ENST00000269209 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:177247810 G>A maps to NM_021165.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:177249586 C>G maps to NM_021165.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr1:177247762 C>T maps to NM_021165.2 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr1:177247922 T>G did not map to a codon.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr1:190068041 G>A maps to NM_199051.1 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:190129904 C>T maps to NM_199051.1 E359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:190067756 G>A maps to NM_199051.1 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr1:190068161 C>T maps to NM_199051.1 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr1:190067738 A>C maps to NM_199051.1 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr1:190068110 G>T maps to NM_199051.1 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr1:150972407 C>G maps to NM_001163258.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:150972347 G>A maps to NM_001163258.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:150974655 G>A maps to NM_001163258.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr15:59144161 C>T maps to NM_001040450.1 Q579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr15:59144043 A>G maps to NM_001040450.1 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr15:59144133 T>A maps to NM_001040450.1 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr17:6350811 C>G maps to NM_001195228.1 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:67575860 C>G maps to NM_001193523.1 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr16:67576932 G>T maps to NM_001193523.1 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr16:67575768 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr16:67575415 C>G maps to NM_001193523.1 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr16:67578264 C>T maps to NM_001193523.1 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr16:67580075 C>G maps to NM_001193523.1 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr16:67576461 C>T maps to NM_001193523.1 I611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:24865636 G>C maps to NM_014722.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:24873897 G>C maps to NM_014722.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr6:24850032 C>T maps to NM_014722.2 W315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr20:49211101 G>A maps to NM_080829.2 Q730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:49212712 C>T maps to NM_080829.2 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr20:49218694 G>A maps to NM_080829.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr20:49227395 G>A maps to NM_080829.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr20:49227395 G>A maps to NM_080829.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr20:49221195 C>A maps to NM_080829.2 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr20:49209002 G>A maps to NM_080829.2 Q815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr20:49209656 G>A maps to NM_080829.2 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr20:49212018 G>C maps to NM_080829.2 S642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:119438236 A>C did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr23:119402107 A>G did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr13:114503879 C>T maps to NM_182614.2 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr1:212799106 G>A maps to NM_153606.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr1:212798486 C>T maps to NM_153606.3 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr1:212799610 C>T maps to NM_153606.3 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:212798590 G>A maps to NM_153606.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:212798813 C>T maps to NM_153606.3 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:212798582 C>T maps to NM_153606.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr5:156592879 G>C maps to NM_130899.2 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr12:100042311 G>C maps to NM_153364.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr19:50978630 A>G maps to ENST00000391816 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr7:128355644 G>T maps to NM_032599.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:128355597 G>T maps to NM_032599.2 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:128355535 C>G maps to NM_032599.2 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr7:128317839 G>A maps to NM_001012454.3 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:128317716 C>A maps to NM_001012454.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr7:128315730 C>T maps to NM_001012454.3 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr1:78267137 A>G maps to NM_198549.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:78269065 C>G maps to NM_198549.2 S162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr1:78340673 G>A maps to NM_198549.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr9:131832214 C>T maps to NM_032809.2 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr9:43627186 C>T maps to NM_001145196.1 Q500Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr9:43625184 G>A maps to NM_001145196.1 Q1168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr9:43625134 C>T maps to NM_001145196.1 E1184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr9:90535925 A>C maps to NM_001145124.1 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr1:28086045 T>C maps to NM_001143912.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:28071218 C>T maps to NM_001143912.1 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr11:95516320 A>T maps to NM_144664.4 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr11:95504793 G>C maps to NM_144664.4 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr9:134136631 G>A maps to NM_033387.3 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:166039522 C>T maps to NM_001017961.3 W247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr5:94756034 T>C maps to NM_152548.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr2:38177729 G>A maps to NM_144713.3 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr15:41037302 G>A maps to NM_018145.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:41044230 C>G maps to NM_018145.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr15:41029864 G>A maps to NM_018145.1 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:87486537 C>T maps to NM_016033.2 *315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:87486542 C>T maps to NM_016033.2 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr8:87498731 G>C maps to NM_016033.2 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:54806294 C>T maps to NM_001010872.1 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr6:54806085 C>T maps to NM_001010872.1 Q773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:33875385 G>C maps to NM_178468.4 S399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:33874439 G>C maps to NM_178468.4 V714V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WY-01A-11D-A22Z-08 chr20:33879831 G>A maps to NM_178468.4 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr20:37580731 C>T maps to NM_030919.2 Q473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:37576604 G>A maps to NM_030919.2 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:37580798 C>G maps to NM_030919.2 S495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:49104485 G>A maps to NM_017708.3 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr22:40415272 C>T maps to NM_138435.2 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr22:40415260 C>T maps to NM_138435.2 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr22:40415994 G>A maps to NM_138435.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr17:18880970 G>A maps to NM_001039999.2 Q670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr17:18907092 G>A maps to NM_001039999.2 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr17:18882042 G>T maps to NM_001039999.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr8:144808669 G>A maps to NM_198488.3 F987F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr8:144808765 C>T maps to NM_198488.3 P955P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr8:144808837 C>T maps to NM_198488.3 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:14774213 C>T maps to NM_145175.2 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr2:14774708 C>G maps to NM_145175.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr2:14774945 C>G maps to NM_145175.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:127569331 C>T maps to NM_174911.4 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr8:127569295 G>A maps to NM_174911.4 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr8:127568857 C>T maps to NM_174911.4 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr8:127569334 G>C maps to NM_174911.4 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr8:127569343 G>A maps to NM_174911.4 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:65341110 G>A maps to NM_001098785.1 *190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr6:17601038 C>T maps to NM_016255.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr12:8375059 G>C maps to NM_018088.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr12:8375059 G>C maps to NM_018088.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr12:8374888 C>G maps to NM_018088.3 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr12:8375059 G>A maps to NM_018088.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr12:8376742 C>T maps to NM_018088.3 W64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr12:8375059 G>C maps to NM_018088.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr8:124810337 C>T maps to NM_144963.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr8:124796787 C>G maps to NM_144963.2 S261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr8:124787453 C>T maps to NM_144963.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr8:124799529 C>T maps to NM_144963.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr8:124812010 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr8:124818392 C>T maps to NM_144963.2 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr8:124812069 C>G maps to NM_144963.2 S585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr8:124787453 C>T maps to NM_144963.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr16:85143909 G>A maps to ENST00000393246 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:33813493 G>A maps to ENST00000395190 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr19:38896258 G>A maps to NM_174905.3 W245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr19:38893807 G>A maps to NM_174905.3 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr19:38896244 A>T maps to NM_174905.3 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr19:38897653 G>T maps to NM_174905.3 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr23:8995956 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr23:8997435 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr23:13061300 A>T did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:13058007 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:13056576 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:89862343 G>A maps to NM_000135.2 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr16:89869699 C>G maps to NM_000135.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr16:89813087 C>T maps to NM_000135.2 L1139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr16:89857864 G>C maps to NM_000135.2 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr16:89816262 G>A maps to NM_000135.2 L1038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr16:89816262 G>A maps to NM_000135.2 L1038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr16:89845228 C>T maps to NM_000135.2 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr16:89858461 C>T maps to NM_000135.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr16:89838137 G>C maps to NM_000135.2 S700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:89813042 G>A maps to NM_000135.2 F1154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr16:89851291 G>A maps to NM_000135.2 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr16:89831450 C>T maps to NM_000135.2 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr23:14863347 C>A did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:14861748 C>T did not map to a codon.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr23:14882864 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:14863384 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr23:14877337 A>G did not map to a codon.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr9:97897750 G>C maps to NM_000136.2 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:10138050 C>G maps to NM_033084.3 L1360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:10127603 C>T maps to NM_033084.3 L1111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr3:10094120 C>G maps to NM_033084.3 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr3:10106107 G>A maps to NM_033084.3 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr6:35426204 C>G maps to NM_021922.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr6:35426106 C>T maps to NM_021922.2 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr6:35426084 G>T maps to NM_021922.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr11:22647303 G>C maps to NM_022725.3 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:22647047 G>A maps to NM_022725.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr9:35077365 G>A maps to NM_004629.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr9:35077034 G>C maps to NM_004629.1 S237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr15:89807247 C>G maps to NM_001113378.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr15:89807247 C>T maps to NM_001113378.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr15:89804928 C>T maps to NM_001113378.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:58425730 G>A maps to NM_001114636.1 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:45605470 G>A maps to NM_020937.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr14:45658432 G>C maps to NM_020937.2 L1736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr14:45605268 G>A maps to NM_020937.2 W12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr14:45645028 C>A maps to NM_020937.2 P1024P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr14:45645526 C>G maps to NM_020937.2 L1190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr14:45642406 C>T maps to NM_020937.2 H770H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr14:45658162 A>C maps to NM_020937.2 A1646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr14:45605330 C>T maps to NM_020937.2 Q33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr14:45644761 T>C maps to NM_020937.2 S935S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr10:127684013 C>T maps to ENST00000368692 H141H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr2:163029726 G>C maps to NM_004460.2 S680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr2:163076435 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:13732281 G>A maps to NM_032228.5 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr11:13729535 C>G maps to NM_032228.5 S152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SU-01A-31D-A391-08 chr11:13743294 T>C maps to NM_032228.5 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr12:29469825 G>A maps to NM_018099.3 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr12:29485661 T>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr13:99092954 G>A maps to NM_005766.2 Q887Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:99083316 G>A maps to NM_005766.2 W642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr13:99037048 C>T maps to NM_005766.2 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr13:99020426 C>T maps to NM_005766.2 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr13:98865513 G>A maps to NM_005766.2 Q6Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr13:99040641 C>T maps to NM_005766.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr13:99040716 C>G maps to NM_005766.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr2:242373631 C>T maps to NM_014808.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr2:242415380 G>A maps to NM_014808.2 E747E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:5368820 C>T maps to NM_006567.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr19:13035074 C>T maps to NM_004461.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr2:223513456 A>G did not map to a codon.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr10:90750653 C>T maps to NM_000043.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:172628517 G>A maps to NM_000639.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:80041239 G>A maps to NM_004104.4 N1801N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:80043455 G>A maps to NM_004104.4 L1342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr17:80047251 C>T maps to NM_004104.4 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr7:150775944 C>G maps to NM_006712.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr7:150774981 G>A maps to NM_006712.3 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr7:150773874 G>C maps to NM_006712.3 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr2:170411685 G>A maps to NM_024622.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr2:170387906 G>C maps to NM_024622.3 S761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr2:170394619 C>T maps to NM_024622.3 Q659Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T4-01A-11D-A391-08 chr2:170387986 G>A maps to NM_024622.3 I734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr2:207652751 C>T maps to NM_014929.3 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7N-01A-11D-A391-08 chr5:7859576 G>A maps to NM_024091.3 Q654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:7867566 T>C maps to NM_024091.3 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BS-01A-21D-A26M-08 chr20:3127436 G>A maps to NM_021826.4 F760F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr20:3128234 G>C maps to NM_021826.4 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:3128966 G>C maps to NM_021826.4 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr20:3129476 G>A maps to NM_021826.4 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr4:187524926 G>A maps to ENST00000260147 Q3588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr4:187540590 G>C maps to ENST00000260147 L2386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr4:187541653 G>T maps to ENST00000260147 S2032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr4:187549508 G>A maps to ENST00000260147 Q1537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr4:187549806 G>T maps to ENST00000260147 I1478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr4:187539563 G>A maps to ENST00000260147 R2729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr4:187518863 G>A maps to ENST00000260147 Q4117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr4:187630569 G>A maps to ENST00000260147 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr4:187525599 C>A maps to ENST00000260147 P3496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr4:187524559 G>C maps to ENST00000260147 S3710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr4:187518320 G>A maps to ENST00000260147 Q4128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr4:187534350 G>A maps to ENST00000260147 F3128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr4:187525000 G>C maps to ENST00000260147 S3563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr4:187521282 G>A maps to ENST00000260147 Q3961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr4:187540390 G>C maps to ENST00000260147 S2453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr4:187542920 C>A maps to ENST00000260147 G1610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr4:187524559 G>T maps to ENST00000260147 S3710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr4:187540254 G>A maps to ENST00000260147 N2498N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr4:187629052 C>T maps to ENST00000260147 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr4:187517721 C>T maps to ENST00000260147 Q4327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr4:187628100 G>A maps to ENST00000260147 Q961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:187538245 G>A maps to ENST00000260147 I2999I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr5:150925746 G>A maps to NM_001447.2 I1647I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr5:150934192 G>A maps to NM_001447.2 T1225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr5:150934192 G>A maps to NM_001447.2 T1225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:150947808 C>T maps to NM_001447.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr5:150889706 G>A maps to NM_001447.2 F3978F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr5:150886889 G>A maps to NM_001447.2 L4114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr5:150891747 C>T maps to NM_001447.2 K3961K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr5:150946089 G>A maps to NM_001447.2 S801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr5:150935958 G>T maps to NM_001447.2 L1193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr5:150925436 C>A maps to NM_001447.2 E1751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr5:150924366 A>T maps to NM_001447.2 Y2107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr5:150897309 G>A maps to NM_001447.2 F3778F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr5:150885416 G>A maps to NM_001447.2 P4253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr5:150922707 G>A maps to NM_001447.2 F2660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr5:150923958 G>C maps to NM_001447.2 V2243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr5:150924129 G>C maps to NM_001447.2 L2186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr5:150924173 G>A maps to NM_001447.2 Q2172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:92087449 T>G maps to ENST00000298047 Y724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:92534005 C>T maps to ENST00000298047 V2609V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:92616260 C>T maps to ENST00000298047 R4213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:92086976 C>T maps to ENST00000298047 R567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:92534509 A>C maps to ENST00000298047 P2777P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr11:92086561 G>C maps to ENST00000298047 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr11:92087971 C>T maps to ENST00000298047 A898A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:92616452 G>A maps to ENST00000298047 R4277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr11:92616248 C>T maps to ENST00000298047 F4209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr11:92570843 C>T maps to ENST00000298047 L3414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr11:92616347 G>A maps to ENST00000298047 Q4242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr11:92088253 C>T maps to ENST00000298047 I992I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr11:92531923 C>T maps to ENST00000298047 P1915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:92616245 G>A maps to ENST00000298047 P4208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr11:92086015 G>T maps to ENST00000298047 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:92564866 C>A maps to ENST00000298047 I3187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr11:92565070 C>G maps to ENST00000298047 V3255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr11:92533568 C>T maps to ENST00000298047 L2464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr11:92087887 C>T maps to ENST00000298047 V870V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr11:92577488 C>A maps to ENST00000298047 R3652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr4:126242012 G>T maps to NM_024582.4 E1483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr4:126398432 C>T maps to NM_024582.4 V4139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr4:126371890 C>G maps to NM_024582.4 L3240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr4:126336817 C>T maps to NM_024582.4 R2234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr4:126398322 C>T maps to NM_024582.4 Q4103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr4:126337751 C>A maps to NM_024582.4 V2331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr4:126411828 G>T maps to NM_024582.4 E4618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr4:126237763 G>C maps to NM_024582.4 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:126371441 C>T maps to NM_024582.4 Q3091*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DK-A6AW-01A-11D-A30E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr4:126373057 C>T maps to NM_024582.4 P3629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:126372223 G>A maps to NM_024582.4 K3351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:126411453 C>T maps to NM_024582.4 Q4493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:126238819 C>T maps to NM_024582.4 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:126238825 C>T maps to NM_024582.4 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:126239281 C>G maps to NM_024582.4 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:126239577 C>G maps to NM_024582.4 S671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:126239779 C>A maps to NM_024582.4 V738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:126240343 C>A maps to NM_024582.4 G926G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:126240562 C>G maps to NM_024582.4 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:126241102 C>G maps to NM_024582.4 V1179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr4:126238268 C>T maps to NM_024582.4 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr4:126239450 C>A maps to NM_024582.4 R629R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr4:126238717 C>T maps to NM_024582.4 D384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr4:126371113 T>C maps to NM_024582.4 P2981P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr4:126240574 C>T maps to NM_024582.4 V1003V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr4:126373721 C>T maps to NM_024582.4 L3851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr4:126239264 C>T maps to NM_024582.4 Q567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr4:126239632 C>T maps to NM_024582.4 F689F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr4:126371953 G>A maps to NM_024582.4 K3261K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr4:126371927 C>T maps to NM_024582.4 Q3253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr4:126239152 C>T maps to NM_024582.4 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr4:126412187 C>A maps to NM_024582.4 T4737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr4:126372606 C>A maps to NM_024582.4 S3479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr4:126240796 G>A maps to NM_024582.4 V1077V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr4:126371548 C>A maps to NM_024582.4 Y3126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr4:126401009 C>A maps to NM_024582.4 Y4196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr23:150891176 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:150891173 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:150891135 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr23:150885799 G>T did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:73914309 G>A maps to ENST00000389570 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr17:73909786 C>T maps to ENST00000389570 Q1067Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr17:73906804 C>T maps to ENST00000389570 *1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr19:40331066 C>T maps to NM_001436.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:40331078 C>A maps to NM_001436.3 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:16111107 C>G maps to NM_017556.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr1:16095060 C>G maps to NM_017556.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr3:13669416 C>T maps to NM_001165035.1 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:13670761 C>T maps to NM_001165035.1 Q938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr2:112944788 C>A maps to NM_153214.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:112896279 C>T maps to NM_153214.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr15:48826366 G>A maps to NM_000138.4 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr15:48752455 G>C maps to NM_000138.4 T1761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:48720648 C>T maps to NM_000138.4 T2297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr15:48782132 T>C maps to NM_000138.4 R999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr15:48805818 A>G maps to NM_000138.4 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr15:48905225 G>T maps to NM_000138.4 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr15:48780690 C>A did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr15:48818330 G>A maps to NM_000138.4 C328C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr15:48714203 G>C maps to NM_000138.4 G2505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr15:48729224 G>A maps to NM_000138.4 I2143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr15:48757825 C>T maps to NM_000138.4 G1627G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr5:127622436 G>A maps to NM_001999.3 R2329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr5:127622541 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr5:127681160 G>A maps to NM_001999.3 T1035T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr5:127730941 C>T maps to NM_001999.3 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr5:127685048 A>G maps to NM_001999.3 R993R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr5:127653963 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr5:127595502 C>A maps to NM_001999.3 E2795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr5:127674744 C>A maps to NM_001999.3 E1118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr5:127627251 A>G maps to NM_001999.3 F2087F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:8136969 G>T maps to NM_032447.3 R2684R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr19:8193910 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:8175798 G>A maps to NM_032447.3 N1421N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr19:8201323 G>A maps to NM_032447.3 Y431Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr19:8188892 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr19:8161816 G>A maps to NM_032447.3 Y1787Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr19:8206967 G>A maps to NM_032447.3 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr19:8191376 C>T maps to NM_032447.3 G843G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr19:8201104 G>A maps to NM_032447.3 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr19:8161885 G>A maps to NM_032447.3 V1764V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr19:8140074 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:8151209 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr19:8191376 C>T maps to NM_032447.3 G843G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr19:8145967 G>A maps to NM_032447.3 Q2458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr19:8139985 G>A maps to NM_032447.3 F2557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr19:8155061 G>C maps to NM_032447.3 T2035T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:8131096 C>T maps to NM_032447.3 L2712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr9:97355852 G>A maps to NM_003837.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:30677858 G>A maps to ENST00000356166 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr7:102553589 C>T maps to NM_145032.3 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr7:102462557 G>T maps to NM_145032.3 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr12:1702938 G>A maps to NM_152441.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr12:1702296 G>A maps to NM_152441.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:1702041 C>T maps to NM_152441.2 E397E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr16:746931 C>T maps to NM_153350.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr5:107559914 T>C maps to NM_001163315.2 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr7:5540318 G>A maps to ENST00000312577 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr7:5540381 G>A maps to ENST00000312577 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr16:30937179 C>T maps to NM_001099784.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr3:33416784 C>T maps to NM_012157.3 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr3:33406160 G>A maps to NM_012157.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr3:33414760 T>C maps to NM_012157.3 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr3:33425581 C>T maps to NM_012157.3 C351C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr17:37427046 A>T did not map to a codon.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr17:37457265 C>T maps to NM_032875.2 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:77581815 G>A maps to NM_012158.2 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr13:77589586 G>C maps to NM_012158.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr13:77581699 T>C maps to NM_012158.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr6:99347251 T>C maps to NM_012160.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:99347211 G>A maps to NM_012160.3 Q417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr4:15626987 A>C maps to NM_012161.3 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:145580112 G>A maps to NM_012162.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr8:145579211 G>A maps to NM_012162.1 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr8:145582011 C>T maps to NM_012162.1 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr8:145582011 C>G maps to NM_012162.1 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr5:15936773 C>T maps to NM_012304.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr5:15928374 C>T maps to NM_012304.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr5:15936964 C>T maps to NM_012304.3 N382N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:67195735 C>T maps to NM_018378.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr16:67197578 C>T maps to NM_018378.2 C327C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr16:67197479 C>T maps to NM_018378.2 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr9:37537105 C>A did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr9:37529145 G>A maps to NM_012166.2 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr9:37529146 G>A maps to NM_012166.2 I560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:48046148 C>T maps to NM_001190274.1 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr2:48035566 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr8:28304752 G>A maps to NM_172366.2 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr10:5958226 C>T maps to NM_032807.3 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr10:5945103 C>T maps to NM_032807.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr10:5979158 C>T maps to NM_032807.3 S1067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr10:5959559 G>A maps to NM_032807.3 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr10:5952974 C>G maps to NM_032807.3 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr10:5951127 A>G maps to NM_032807.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:11708843 G>A maps to NM_012168.4 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:11708768 G>A maps to NM_012168.4 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr1:11708840 G>A maps to NM_012168.4 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:117610322 G>C maps to NM_033624.2 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:117595694 G>A maps to NM_033624.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr12:117612050 G>A maps to NM_033624.2 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr12:117628252 C>T maps to NM_033624.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:117604821 C>T maps to NM_033624.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr15:76225118 C>G maps to NM_147188.2 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr15:76225217 G>A maps to NM_147188.2 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr15:76222339 C>T maps to NM_147188.2 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr15:76225157 C>T maps to NM_147188.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr7:100189392 C>T maps to NM_012172.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr7:100187840 C>G maps to NM_012172.4 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr7:100192153 C>G maps to NM_012172.4 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr7:100192084 G>C maps to NM_012172.4 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr8:385663 C>G maps to NM_183421.1 S113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:39521862 G>A maps to NM_178820.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr19:39516068 C>G maps to NM_178820.3 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr19:39516074 C>T maps to NM_178820.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:39521873 G>A maps to NM_178820.3 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr1:224345126 C>T maps to NM_015176.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr11:33763507 C>G maps to NM_012175.3 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr11:33763480 G>A maps to NM_012175.3 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:146121438 G>A maps to NM_032145.4 R681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr8:124553194 G>A maps to NM_058229.2 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr8:124525575 C>T maps to NM_058229.2 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr14:39900842 G>T maps to NM_203301.3 S175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr14:55817980 G>A maps to NM_152231.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr14:55818154 T>C maps to NM_152231.1 D349D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr5:147820705 A>G maps to NM_205836.1 P1098P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr3:121345736 C>T maps to NM_016298.3 R704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr3:121345705 G>A maps to NM_016298.3 E693E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr2:73495885 C>A maps to ENST00000295133 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr2:73493784 G>A maps to ENST00000295133 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr2:73493785 G>A maps to ENST00000295133 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr2:73493770 C>T maps to ENST00000295133 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:16632349 C>T maps to NM_018994.1 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr1:16578085 C>T maps to NM_018994.1 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:16632312 G>A maps to NM_018994.1 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:16579617 G>A maps to NM_018994.1 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr1:16641715 C>T maps to NM_018994.1 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr1:16578100 G>A maps to NM_018994.1 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:101153668 T>C maps to NM_001029860.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:101153838 C>A maps to NM_001029860.3 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:101154328 C>T maps to NM_001029860.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr1:11716153 G>T maps to ENST00000376768 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr3:196311152 G>A maps to NM_001105573.1 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:46216532 G>C maps to NM_001080469.1 S74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr19:46216735 G>A maps to NM_001080469.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:46215529 G>T maps to NM_001080469.1 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr17:37119251 G>A maps to NM_001008777.2 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:153296352 G>A maps to NM_012177.3 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:11728997 G>T maps to NM_018438.5 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr22:32879975 C>T maps to NM_012179.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr22:32889254 G>A maps to NM_012179.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr22:32871362 C>G maps to NM_001033024.1 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr6:52957256 G>A maps to NM_012347.4 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:18668066 G>T maps to ENST00000395665 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:18653218 C>G maps to ENST00000395665 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:48423543 G>T maps to NM_207102.2 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr3:48423352 C>T maps to NM_207102.2 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr3:48423524 C>A maps to NM_207102.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:123550365 G>C maps to NM_012164.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:123527034 G>A maps to NM_012164.3 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr9:123540761 G>A maps to NM_012164.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr10:103433333 C>T maps to ENST00000331272 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr10:103371486 G>A maps to ENST00000331272 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr9:139835999 C>T maps to NM_018998.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr9:139836092 G>A maps to NM_018998.2 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr9:139836609 G>A maps to NM_018998.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr4:153253769 C>T maps to NM_033632.2 W321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr4:153244123 G>C maps to NM_033632.2 S678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr4:153244234 G>C maps to NM_033632.2 S641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:153332523 C>T maps to NM_033632.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr4:153247279 G>A maps to NM_033632.2 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr4:153273675 C>T maps to NM_018315.4 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr4:153332576 G>A maps to NM_033632.2 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr4:153244184 G>A maps to NM_033632.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr4:153273870 C>T maps to NM_018315.4 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr4:153258982 G>A maps to NM_033632.2 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr4:153251910 C>T maps to NM_033632.2 W365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr4:153247366 G>A maps to NM_033632.2 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr4:153332915 G>A maps to NM_033632.2 R14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr4:153273858 C>T maps to NM_018315.4 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr12:117365826 G>A did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr19:12800095 A>T maps to ENST00000380339 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr19:12800191 G>A maps to ENST00000380339 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr19:12805723 G>A maps to ENST00000380339 C146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr19:12807342 G>T maps to ENST00000380339 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:207135776 G>A maps to NM_001170631.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr19:55396830 C>T maps to NM_002000.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr19:55386784 G>C did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr19:55401021 C>T maps to NM_002000.2 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:159273847 C>T maps to ENST00000368115 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr1:159273883 G>A maps to ENST00000368115 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:7762140 C>T maps to NM_002002.4 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:75182719 C>T maps to NM_015962.4 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:40408700 C>A maps to NM_003890.2 G1380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr19:40368729 G>A maps to NM_003890.2 P4206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr19:40421169 C>T maps to NM_003890.2 V917V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:40408602 G>C maps to NM_003890.2 A1412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:40376655 C>T maps to NM_003890.2 E3922E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:40392508 G>C maps to NM_003890.2 L2665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr19:40360984 G>C maps to NM_003890.2 L5141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr19:40392610 C>T maps to NM_003890.2 P2631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr19:40368624 G>A maps to NM_003890.2 I4241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr19:40357463 G>A maps to NM_003890.2 I5283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:40368510 G>A maps to NM_003890.2 F4279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:40433167 G>A maps to NM_003890.2 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr19:40411865 C>T maps to NM_003890.2 A1254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:40354439 C>T maps to NM_003890.2 K5343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:40434058 G>A maps to NM_003890.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr19:40395941 G>A maps to NM_003890.2 T2485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr19:40392066 G>A maps to NM_003890.2 F2773F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr1:149760119 C>G maps to NM_000566.3 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr1:149763000 G>A maps to NM_000566.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:120930096 G>A maps to NM_001017986.2 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr1:161480705 T>A maps to NM_001136219.1 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:161476236 C>T maps to NM_001136219.1 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:161641317 C>G maps to NM_004001.4 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:161641407 C>T maps to NM_004001.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr1:161641371 C>T maps to NM_004001.4 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:161641317 C>T maps to NM_004001.4 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:161596034 A>T maps to ENST00000367964 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:50017148 C>T maps to NM_004107.4 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr19:50017193 G>A maps to NM_004107.4 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr19:17892530 G>A maps to NM_015122.2 R613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:17886293 C>T maps to NM_015122.2 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr19:17877489 G>T maps to NM_015122.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr5:72383915 G>C maps to NM_138782.2 *811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr5:72359713 G>A maps to NM_138782.2 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr11:72551972 G>A maps to ENST00000409314 F720F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr11:72726930 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:137804335 G>C maps to NM_002003.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr9:137804954 C>T maps to NM_002003.3 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:137809708 C>G maps to NM_002003.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr9:137801700 C>T maps to NM_002003.3 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr9:137777142 C>A maps to NM_004108.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:137777708 G>A maps to NM_004108.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr9:137777211 C>T maps to NM_004108.2 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:137779143 G>C maps to NM_004108.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:27695778 G>C maps to NM_003665.2 S283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:157776904 G>A maps to NM_052938.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:157766902 A>G maps to NM_052938.4 H402H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr1:157738477 A>G maps to NM_030764.3 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr1:157739893 G>A maps to NM_030764.3 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr1:157737210 C>T maps to NM_030764.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:157665208 G>A maps to NM_052939.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:157650525 C>T maps to NM_052939.3 Q664Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:157660180 C>T maps to NM_052939.3 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:157557730 A>G maps to NM_031282.2 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:157490993 C>T maps to NM_031281.2 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr1:157514223 G>C maps to NM_031281.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr1:157514226 C>T maps to NM_031281.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:157514313 C>T maps to NM_031281.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr1:157514816 C>G maps to NM_031281.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr1:159784074 G>A maps to NM_001004310.2 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr1:159777974 G>A maps to NM_001004310.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:161681928 C>T maps to NM_001184866.1 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:161681202 C>A maps to NM_001184866.1 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:161697034 A>T did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:161696643 G>A maps to NM_001002901.2 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr1:161697271 G>A maps to NM_001002901.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:161695647 C>T maps to NM_001002901.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:161696694 C>T maps to NM_001002901.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:161696748 G>A maps to NM_001002901.2 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr11:111746265 G>A maps to NM_138378.1 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:111749796 C>T maps to ENST00000428306 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr17:72859252 G>A maps to ENST00000442102 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr17:72859207 G>A maps to ENST00000442102 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:72861002 C>T maps to ENST00000442102 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr18:55226415 C>T maps to NM_001012515.2 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr18:55218000 G>C maps to NM_001012515.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr19:4792856 C>T maps to NM_018708.2 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:4792708 G>A maps to NM_018708.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:4793480 C>T maps to NM_018708.2 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:4792858 G>A maps to NM_018708.2 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr15:68582397 C>T maps to NM_015322.3 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr15:68582601 T>C maps to NM_015322.3 Y302Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr15:68583477 G>A maps to NM_015322.3 K594K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:114879142 G>A maps to NM_020177.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:114860256 G>A maps to NM_020177.2 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr5:108436118 G>A maps to NM_005246.2 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr5:108436172 C>T maps to NM_005246.2 D667D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr5:108290633 G>A did not map to a codon.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr2:97370380 A>G maps to NM_001113382.1 T2078T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:97368023 C>G maps to NM_001113382.1 S1750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr8:125022908 C>T maps to NM_001039112.2 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:124975539 A>C maps to NM_001039112.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr8:125113409 C>T maps to NM_001039112.2 N1652N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr8:125058087 G>A maps to NM_001039112.2 E890E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr8:125082840 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr8:125107170 C>T maps to NM_001039112.2 L1529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr8:125025759 C>T maps to NM_001039112.2 I637I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr8:125047529 C>T maps to NM_001039112.2 R767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr8:125035721 C>G maps to NM_001039112.2 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr7:19184847 G>A maps to NM_152898.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr20:6057945 C>T maps to NM_017671.4 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SU-01A-31D-A391-08 chr20:6068459 G>A maps to NM_017671.4 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr20:6065826 C>T maps to NM_017671.4 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr20:6078251 G>A maps to NM_017671.4 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr14:53386042 G>C maps to NM_001134999.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr14:53347816 C>G maps to NM_001134999.1 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr14:53386037 C>T maps to NM_001134999.1 W65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:63974871 C>T maps to NM_178443.2 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr11:63990597 C>T maps to NM_178443.2 D587D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr11:63990555 C>T maps to NM_178443.2 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr11:63978861 C>T maps to NM_178443.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr15:91428340 C>T maps to NM_002005.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr15:91432631 C>T maps to NM_002005.3 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr3:186370287 G>T maps to NM_014375.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr3:186369029 T>C maps to NM_014375.2 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:186362597 C>T maps to NM_014375.2 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr3:186362657 G>A maps to NM_014375.2 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr11:125333377 A>G did not map to a codon.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr7:121942122 C>T maps to NM_001024613.2 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:62357988 G>C maps to NM_018008.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:62357988 G>C maps to NM_018008.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:35842753 G>A maps to NM_005303.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:35940870 G>A maps to NM_005306.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:35940648 C>T maps to NM_005306.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr19:35850451 G>A maps to NM_005304.3 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr19:35850668 A>C maps to NM_005304.3 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr4:155506819 C>G maps to NM_000508.3 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr4:155508039 G>A maps to NM_000508.3 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr4:155505985 C>G did not map to a codon.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr23:54496453 C>A did not map to a codon.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr23:54497827 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:54473865 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr23:54496794 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr23:54496483 G>A did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr23:54491998 C>G did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr23:54472665 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:54482986 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:36982666 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr6:36995302 G>T maps to NM_173558.3 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:95784613 G>A maps to NM_033086.2 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:95738560 C>G maps to NM_033086.2 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr9:95772610 C>T maps to NM_033086.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr9:95778074 C>T maps to NM_033086.2 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:32760949 G>T maps to NM_139241.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr12:32751510 C>G maps to NM_139241.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:14941940 C>G maps to NM_152536.3 A1062A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:14862488 G>T maps to NM_152536.3 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr3:14862506 G>A maps to NM_152536.3 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:95603477 C>A maps to NM_018351.3 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:95485585 C>G did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr5:44388752 G>C maps to NM_004465.1 S11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr3:191888333 C>A maps to NM_021032.4 G176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr3:191861851 A>G maps to NM_021032.4 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr3:192125826 C>T maps to NM_021032.4 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:191888292 C>T maps to NM_021032.4 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:192125871 C>T maps to NM_021032.4 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:138286238 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr23:137939731 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr23:137717742 A>G did not map to a codon.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr23:137790982 A>T did not map to a codon.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr23:137715035 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr23:137715049 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr13:103053995 A>T maps to NM_175929.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:103054019 T>C maps to NM_175929.2 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr13:102521170 G>A maps to NM_175929.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:76709727 G>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:76709655 G>C did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr5:170883751 C>T maps to NM_003862.2 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr4:123813436 G>A maps to NM_002006.4 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr8:16859520 G>A maps to NM_019851.2 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:49259603 C>T maps to NM_019113.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr12:4479898 G>A maps to NM_020638.2 N122N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:4479727 C>A maps to NM_020638.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:81207684 G>A maps to NM_004464.3 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr10:103534600 G>C maps to NM_033163.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr10:103530307 C>T maps to NM_033163.3 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr4:15937937 G>C maps to NM_005130.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:38271716 C>T maps to NM_001174067.1 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr8:38279348 G>A maps to NM_001174067.1 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr10:123258015 T>C maps to ENST00000351936 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr10:123310938 T>C maps to ENST00000351936 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr10:123276935 G>C maps to ENST00000357555 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr10:123279495 G>A maps to ENST00000351936 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr4:1808043 C>T maps to NM_000142.4 Q674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr4:1807558 C>T maps to NM_000142.4 D576D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr4:1806087 G>T maps to NM_000142.4 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr4:1803655 C>T maps to NM_000142.4 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr4:1801110 G>A maps to NM_000142.4 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr4:1806111 C>T maps to NM_000142.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr4:1804678 C>A maps to NM_001163213.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:176523643 C>T maps to NM_213647.1 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr5:176520307 C>T maps to NM_213647.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr4:1018309 C>T maps to NM_021923.3 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr4:1016162 G>A maps to NM_021923.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr4:155526063 C>T maps to ENST00000407946 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr4:155530853 C>T maps to ENST00000407946 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr4:155527887 G>A maps to ENST00000407946 H374H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr1:60139744 C>G maps to NM_001113411.1 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:60139744 C>G maps to NM_001113411.1 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:60228254 G>C maps to NM_001113411.1 *576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:60139744 C>G maps to NM_001113411.1 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr8:17739538 G>A maps to NM_201552.1 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:17739571 G>C maps to NM_201552.1 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr8:17731904 G>A maps to NM_201552.1 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:76828690 C>G maps to NM_006682.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:27950378 C>A maps to NM_005248.2 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr1:27941025 G>T maps to NM_005248.2 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr1:27948110 G>A maps to NM_005248.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:241675334 C>A maps to NM_000143.3 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:241665790 G>T maps to NM_000143.3 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:153897463 C>T maps to NM_033393.2 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:153896614 G>A maps to NM_033393.2 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr4:153893635 G>A maps to NM_033393.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr3:59737966 C>A maps to NM_002012.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr23:135289282 T>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:135291435 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:135290109 A>T did not map to a codon.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr2:105984104 G>A maps to ENST00000344213 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr2:105979820 G>A maps to ENST00000344213 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr2:105977787 G>A maps to ENST00000344213 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:67265986 A>C maps to NM_013241.2 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:33952675 G>A maps to NM_025135.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr18:34310607 G>C did not map to a codon.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr18:34174751 C>T maps to NM_025135.2 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr18:34273301 C>T maps to NM_025135.2 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr9:133780648 G>C maps to NM_001145106.1 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:133799255 G>A maps to NM_001145106.1 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr9:133780795 G>C maps to NM_001145106.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr11:65653031 G>A maps to NM_198897.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr12:108910838 G>A maps to NM_007076.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr12:108912273 C>G maps to NM_007076.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:108912879 A>G maps to NM_007076.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr23:15371213 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr23:15376160 G>C did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr2:164466370 C>A maps to NM_018086.2 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:164467837 A>G maps to NM_018086.2 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:164468308 C>T maps to NM_018086.2 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr2:164466679 T>C maps to NM_018086.2 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr7:50514655 G>A maps to NM_022116.3 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:76124426 C>A maps to NM_015687.2 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr6:76124590 G>C maps to NM_015687.2 S33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr6:76023320 G>A maps to NM_015687.2 Q743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr6:76024128 G>C maps to NM_015687.2 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr6:76063418 C>T maps to NM_015687.2 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr6:76072606 C>T maps to NM_015687.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr6:76024848 G>A maps to NM_015687.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr3:99567198 G>A maps to NM_001042459.1 V1107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr3:99567512 G>A maps to NM_001042459.1 Q1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr4:54280808 A>C maps to NM_030917.3 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr4:54248501 G>A maps to NM_030917.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr7:100884113 G>C maps to NM_016068.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr14:24601572 G>T maps to NM_203402.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr19:56103935 G>C maps to NM_032836.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr19:56104595 G>A maps to NM_032836.2 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr11:35640855 G>A maps to NM_014344.3 Q224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr11:35640996 C>T maps to NM_014344.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr17:39977231 C>T maps to NM_021939.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:39978062 G>A maps to NM_021939.3 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr7:30066097 G>C maps to NM_017946.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr9:115950729 A>G maps to ENST00000446284 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:115930781 C>G maps to ENST00000446284 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:115931550 T>A maps to ENST00000446284 T1171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr20:1352809 G>A maps to NM_054014.3 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr2:24285947 G>A maps to NM_004116.3 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:64010753 C>T maps to NM_057092.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr12:2907948 C>T maps to NM_002014.3 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr6:35586901 G>C maps to NM_001145775.1 S160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr7:72754660 C>T maps to NM_003602.3 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr7:72744160 C>T maps to NM_003602.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:179343040 G>T maps to ENST00000350591 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr2:179330541 G>A maps to ENST00000350591 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr19:18650528 C>T maps to NM_012181.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr7:33028145 G>A maps to NM_007270.3 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr7:33044803 C>T maps to NM_007270.3 H518H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr7:33028193 T>A maps to NM_007270.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr19:47260077 C>T maps to NM_024301.4 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:154962649 T>A maps to NM_025207.4 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:154956262 C>G maps to NM_025207.4 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:154962919 G>A maps to NM_025207.4 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:154956530 G>T maps to NM_025207.4 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:154956262 C>G maps to NM_025207.4 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:17116969 C>G maps to NM_144997.5 *580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr17:17124812 T>C maps to NM_144606.5 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr1:152284481 C>T maps to NM_002016.1 E960E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr1:152281715 C>T maps to NM_002016.1 G1882G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:152285219 G>T maps to NM_002016.1 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr1:152284111 G>A maps to NM_002016.1 Q1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:152285756 C>T maps to NM_002016.1 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr1:152286241 C>A maps to NM_002016.1 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:152276030 C>T maps to NM_002016.1 S3777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:152276090 G>A maps to NM_002016.1 T3757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr1:152277089 G>A maps to NM_002016.1 H3424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr1:152283896 G>A maps to NM_002016.1 H1155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:152282195 G>A maps to NM_002016.1 S1722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:152282165 C>T maps to NM_002016.1 Q1732Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:152284088 C>T maps to NM_002016.1 Q1091Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr1:152275826 G>A maps to NM_002016.1 S3845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr1:152280710 G>T maps to NM_002016.1 A2217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr1:152283713 T>G maps to NM_002016.1 A1216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr1:152284325 A>C maps to NM_002016.1 T1012T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr1:152278757 A>G maps to NM_002016.1 S2868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:152281451 A>T maps to NM_002016.1 S1970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:152283395 A>T maps to NM_002016.1 S1322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr1:152287124 G>A maps to NM_002016.1 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr1:152282757 G>C maps to NM_002016.1 S1535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr1:152280456 G>C maps to NM_002016.1 S2302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr1:152282138 C>A maps to NM_002016.1 G1741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:152278715 C>T maps to NM_002016.1 R2882R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr1:152276117 G>A maps to NM_002016.1 H3748H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr1:152278025 T>C maps to NM_002016.1 G3112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:152326407 G>C maps to NM_001014342.2 S1285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr1:152326142 A>T maps to NM_001014342.2 A1373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr1:152325719 C>T maps to NM_001014342.2 S1514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr1:152324295 G>C maps to NM_001014342.2 S1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr1:152325729 G>C maps to NM_001014342.2 S1511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:152325881 T>A maps to NM_001014342.2 T1460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:152327683 G>A maps to NM_001014342.2 Q860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:152329498 G>A maps to NM_001014342.2 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr1:152327054 A>G maps to NM_001014342.2 S1069S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr11:128642863 C>T maps to NM_002017.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr11:128642863 C>T maps to NM_002017.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr11:128680486 G>A maps to NM_002017.3 W321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr17:18155331 G>A maps to NM_002018.2 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr17:18156959 G>C maps to NM_002018.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr17:18155373 C>T maps to NM_002018.2 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr14:21556226 C>T maps to NM_018071.3 A1496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr14:21541244 C>T maps to NM_018071.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr14:21543088 G>T maps to NM_018071.3 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr8:142490056 G>A maps to NM_207414.2 L310L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-AA77-01A-11D-A391-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-FD-A5BZ-01A-11D-A289-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-FD-A5BZ-01A-11D-A289-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr8:142506564 T>C maps to NM_207414.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr8:142446093 C>G maps to NM_207414.2 L1158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr8:142481284 C>A maps to NM_207414.2 E626*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HQ-A2OF-01A-11D-A26M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr8:142451329 C>T maps to NM_207414.2 Q997Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr9:84609659 C>T maps to NM_001001670.2 I1425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr9:84607085 G>A maps to NM_001001670.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr9:84607838 G>T maps to NM_001001670.2 G818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr9:84606452 C>T maps to NM_001001670.2 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr9:84608318 C>T maps to NM_001001670.2 S978S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr9:84607131 C>T maps to NM_001001670.2 Q583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr9:84606578 C>G maps to NM_001001670.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr9:84606359 G>A maps to NM_001001670.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr23:153581395 C>A did not map to a codon.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:153588176 G>A did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:153580932 G>A did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:153580629 C>A did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:153577784 C>T did not map to a codon.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr23:153592463 C>T did not map to a codon.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr23:153593317 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:153580261 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr23:153595201 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr23:153588463 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr23:153587898 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:153593627 C>G did not map to a codon.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr23:153593529 C>T did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr23:153588565 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:153578565 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr23:153599342 G>C did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:153596244 C>T did not map to a codon.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr23:153588590 G>A did not map to a codon.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr23:153588591 C>G did not map to a codon.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr23:153596051 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:153583034 A>C did not map to a codon.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr23:153585850 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr23:153580034 C>A did not map to a codon.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr23:153577881 A>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr3:58155464 C>T maps to NM_001164317.1 L2553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr3:58120490 C>T maps to NM_001164317.1 Q1586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr3:58062848 C>T maps to NM_001164317.1 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:58109121 C>T maps to NM_001164317.1 L1143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:58106995 C>T maps to NM_001164317.1 F964F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr3:58139210 C>T maps to NM_001164317.1 P2190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:58134448 C>T maps to NM_001164317.1 N2018N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr3:58134541 C>T maps to NM_001164317.1 F2049F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr3:58111395 T>C maps to NM_001164317.1 S1329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr3:58154323 C>T maps to NM_001164317.1 I2483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr3:58095301 G>A did not map to a codon.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr3:57994443 C>T maps to NM_001164317.1 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr3:57994581 C>T maps to NM_001164317.1 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:58141726 C>T maps to NM_001164317.1 I2302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:128490514 G>A maps to NM_001458.4 A1792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr7:128471002 C>G maps to NM_001458.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:128494914 G>T maps to NM_001458.4 E2362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr7:128494235 G>A maps to NM_001458.4 L2231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr7:128485244 C>A maps to NM_001458.4 V1242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr7:128484780 A>T maps to NM_001458.4 K1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr7:128496691 G>T maps to NM_001458.4 E2458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr7:128484746 G>A maps to NM_001458.4 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:128489028 C>T maps to NM_001458.4 L1640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr7:128483609 C>T maps to NM_001458.4 V930V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr7:128470903 C>T maps to NM_001458.4 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr7:128481539 C>A maps to NM_001458.4 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr6:30698321 G>C maps to NM_005803.2 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr17:27207751 G>A maps to ENST00000394906 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:27207617 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:27207778 G>C maps to ENST00000394906 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr11:63885482 G>T maps to NM_013280.4 E582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr11:63885421 G>T maps to NM_013280.4 V561V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr14:86087956 C>G maps to NM_013231.4 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr14:86088061 C>G maps to NM_013231.4 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr14:86088100 T>C maps to NM_013231.4 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr14:86089432 A>G maps to NM_013231.4 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr14:86088024 C>G maps to NM_013231.4 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr14:86088675 C>A maps to NM_013231.4 S273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr14:86089001 C>T maps to NM_013231.4 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr14:86087880 G>A maps to NM_013231.4 W8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr14:86089504 C>T maps to NM_013231.4 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr20:14307450 C>G maps to NM_198391.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr20:14306970 G>T maps to NM_198391.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7N-01A-11D-A391-08 chr13:28908174 C>T maps to NM_002019.4 V860V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr13:28896410 C>G maps to NM_002019.4 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr13:28897020 C>T maps to NM_002019.4 K953K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr13:29008207 G>C maps to NM_002019.4 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr13:29012387 C>T maps to NM_002019.4 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr13:28589745 C>T maps to NM_004119.2 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr13:28610100 G>A maps to NM_004119.2 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr13:28623558 G>C maps to NM_004119.2 S333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr13:28610151 C>T maps to NM_004119.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:49982224 C>T maps to NM_001459.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr5:180057287 C>T maps to NM_182925.4 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:180048703 G>A maps to NM_182925.4 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr5:180058713 G>A maps to NM_182925.4 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:180041110 G>A maps to NM_182925.4 D1096D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr5:180046740 C>T maps to NM_182925.4 G857G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr5:180040066 G>A maps to NM_182925.4 C1125C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr5:180048836 G>C maps to NM_182925.4 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr5:180057239 A>G maps to NM_182925.4 N166N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:213032135 C>T maps to NM_014053.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:213037119 G>A maps to NM_014053.2 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:213032441 C>T maps to NM_014053.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:213046047 A>G maps to NM_014053.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr14:76045320 G>A maps to NM_017791.2 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:76045554 G>A maps to NM_017791.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:76045893 C>T maps to NM_017791.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:76045401 C>T maps to NM_017791.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr14:76107312 C>A maps to NM_017791.2 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr14:76107348 C>G maps to NM_017791.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr15:33358804 G>C maps to NM_001103184.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:33359340 G>A maps to NM_001103184.2 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:33359295 C>A maps to NM_001103184.2 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr1:240370515 C>T maps to ENST00000406993 Q945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:240372002 C>T maps to ENST00000406993 Y1440Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr1:240256017 C>T maps to ENST00000406993 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr1:240286612 C>T maps to ENST00000406993 Q727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr1:240255998 C>G maps to ENST00000406993 S340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:240341298 C>T maps to ENST00000406993 R764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:240374492 G>A maps to ENST00000406993 K1484K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr1:240371090 C>T maps to ENST00000406993 P1136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr1:240458165 C>T maps to ENST00000406993 Q1543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr1:240371519 C>T maps to ENST00000406993 P1279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:240370472 G>A maps to ENST00000406993 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:43323890 C>T maps to NM_005892.3 F1077F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr17:43316383 C>T maps to NM_005892.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr17:43309807 C>T maps to NM_005892.3 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr17:43315962 G>A maps to NM_005892.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:153484986 G>A maps to NM_052905.3 Q780Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:153483148 G>C maps to NM_052905.3 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr2:153484917 G>A maps to NM_052905.3 K757K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr12:50059682 C>T maps to NM_175736.4 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr12:50044616 C>T maps to NM_175736.4 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr12:50048042 C>A maps to NM_175736.4 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:171244579 C>T maps to NM_002021.1 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:171251467 G>C maps to NM_002021.1 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:171249989 G>A maps to NM_002021.1 W231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:171178013 G>A maps to NM_001460.2 K446K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:171178010 G>A maps to NM_001460.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:171080102 C>T maps to NM_006894.5 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr1:171077238 C>A maps to NM_006894.5 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:171073095 G>A maps to NM_006894.5 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:171077280 C>T maps to NM_006894.5 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr1:171310782 G>A maps to NM_002022.1 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:171310692 A>G maps to NM_002022.1 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr1:171303597 C>A maps to NM_002022.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:146672878 G>C maps to NM_001461.2 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr23:147014277 A>G did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr23:147024794 A>T did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:147106394 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:147088241 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:147088267 G>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr2:216248845 G>A maps to NM_212482.1 S1597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr2:216248800 G>A maps to NM_212482.1 V1612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr2:216249685 C>T maps to NM_212482.1 P1542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr2:216256418 C>T maps to NM_212482.1 V1396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr2:216243954 G>A maps to NM_212482.1 L1840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:216271123 C>T maps to NM_212482.1 V941V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:216240427 G>A maps to NM_212482.1 G1967G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr2:216289907 G>C maps to NM_212482.1 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr2:216236838 C>T maps to NM_212482.1 P2169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr2:216279616 G>A maps to NM_212482.1 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr2:216236757 G>T maps to NM_212482.1 L2196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr2:216284072 G>A maps to NM_212482.1 Q571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr17:80706837 C>G maps to NM_022158.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr17:80708414 C>T maps to NM_022158.3 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr17:80684716 C>A maps to NM_024619.3 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr17:80676927 G>C maps to NM_024619.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr9:132658258 C>T maps to NM_015033.2 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:47745703 G>A maps to NM_015308.2 I780I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr6:159682220 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:159677591 C>T maps to NM_032532.2 I1701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr6:159655129 C>T maps to NM_032532.2 L1196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr6:159653693 C>G maps to NM_032532.2 S717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr6:159653934 C>T maps to NM_032532.2 G797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr6:159672433 C>A maps to NM_032532.2 P1645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr6:159687272 G>A maps to NM_032532.2 L1814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:159650895 C>T maps to NM_032532.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr3:171969089 A>C maps to NM_022763.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:172080473 C>T maps to NM_022763.3 F949F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:172080548 G>T maps to NM_022763.3 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr3:172025173 C>G maps to NM_022763.3 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:172070669 C>T maps to NM_022763.3 V864V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr3:172062048 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr2:27717244 G>T maps to NM_022823.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr2:27716337 G>A maps to NM_022823.2 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:109271378 C>T maps to NM_001144937.1 Q499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:109270676 C>T maps to NM_001144937.1 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr17:33454291 G>A maps to NM_017559.2 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr17:33454282 G>A maps to NM_017559.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:130982829 C>G maps to NM_133372.2 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr5:131006320 T>C maps to NM_133372.2 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:130980456 C>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:131007432 G>A maps to NM_133372.2 Q902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr5:131007604 G>A maps to NM_133372.2 I844I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:65521358 C>T maps to ENST00000448390 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr14:65528023 C>T maps to ENST00000448390 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr14:65507600 C>T maps to ENST00000448390 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr11:49227725 T>G did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:49176029 G>A maps to NM_004476.1 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:49179592 C>G maps to NM_004476.1 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr11:49176017 T>C maps to NM_004476.1 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr11:49175903 G>T maps to NM_004476.1 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr11:49227662 T>G maps to NM_004476.1 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:89424063 C>T maps to NM_153696.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:89424103 G>T maps to NM_153696.2 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr11:89424090 C>A maps to NM_153696.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr11:89402620 C>T maps to NM_153696.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:71932541 C>T maps to NM_001113536.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr14:75745826 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:75746725 C>T maps to NM_005252.3 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr14:75747934 C>A maps to NM_005252.3 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr19:45976149 G>A maps to NM_006732.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr19:45976194 C>T maps to NM_006732.2 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:45976194 C>T maps to NM_006732.2 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr11:65660634 C>A maps to NM_005438.3 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr2:28627026 C>T maps to NM_005253.3 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr2:28616604 C>T maps to NM_005253.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:38060824 C>T maps to NM_004496.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr14:38064162 C>T maps to NM_004496.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr20:22563276 G>A maps to NM_021784.4 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:22562718 G>A maps to NM_021784.4 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:22562625 G>A maps to NM_021784.4 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr19:46375734 C>T maps to NM_004497.2 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:46375739 G>A maps to NM_004497.2 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr19:46375805 C>T maps to NM_004497.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr9:79635343 G>A maps to NM_001013735.1 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr9:79634743 G>A maps to NM_001013735.1 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:1612340 G>A maps to NM_001453.2 *554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr6:1612317 C>T maps to NM_001453.2 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr16:86601424 C>T maps to NM_005251.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr1:47904408 G>A maps to NM_004474.3 W201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:63789286 G>A maps to NM_012183.2 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr9:117756 C>T maps to NM_207305.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr9:117909 G>A maps to NM_207305.3 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr2:114256932 G>T maps to NM_012184.4 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:114257297 C>T maps to NM_012184.4 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:70177732 G>C maps to NM_001126334.1 S84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr9:100616369 C>A maps to NM_004473.3 Y58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:47882466 C>T maps to NM_012186.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr16:86544387 G>A maps to NM_001451.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr6:1390559 C>A maps to NM_001452.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr6:1390700 C>T maps to NM_001452.1 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr14:29236559 C>T maps to NM_005249.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr14:29237879 G>A maps to NM_005249.3 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr14:29237360 C>T maps to NM_005249.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr10:129537069 G>A maps to NM_207426.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:74136182 C>T maps to NM_001454.3 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr12:8192481 G>A maps to NM_018416.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr1:42657333 G>A maps to NM_001198850.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr7:4794200 C>T maps to ENST00000450194 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr7:4794947 G>C maps to ENST00000450194 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr7:4800833 C>T maps to ENST00000450194 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr17:80545110 A>T maps to NM_004514.3 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr17:80529634 G>C maps to NM_004514.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:80478009 C>T maps to NM_004514.3 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr17:80559368 G>A maps to NM_004514.3 Q659Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr17:80477931 C>T maps to NM_004514.3 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:80541960 C>T maps to NM_004514.3 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr16:86612649 C>T maps to NM_005250.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:86612412 C>G maps to NM_005250.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:86612808 G>A maps to NM_005250.2 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr3:138665090 C>T maps to NM_023067.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:138665348 C>T maps to NM_023067.3 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:138665348 C>T maps to NM_023067.3 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:2968484 C>T maps to NM_202002.1 E575E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:2983164 G>A maps to NM_202002.1 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr12:2973566 C>T maps to NM_202002.1 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr12:2968460 C>T maps to NM_202002.1 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr17:26861964 C>A maps to NM_003593.2 S459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:26856165 C>T maps to NM_003593.2 Q252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr17:26864384 G>A maps to NM_003593.2 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:48602410 C>A maps to NM_002158.3 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr2:48586220 G>A maps to NM_002158.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:48573385 G>A maps to NM_002158.3 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:48602437 G>A maps to NM_002158.3 K384K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr2:48602107 C>T maps to NM_002158.3 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr14:89878790 C>T maps to NM_001085471.1 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr14:89878714 G>A maps to NM_001085471.1 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr13:41133686 T>C maps to NM_002015.3 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr6:108882524 G>A maps to NM_001455.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr6:108984896 G>A maps to NM_001455.3 Q287Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:108985223 C>T maps to NM_001455.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:108985622 C>T maps to NM_001455.3 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:70316778 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr23:70321315 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr23:70316732 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr23:70316508 C>T did not map to a codon.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr3:71050167 G>T maps to NM_032682.4 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:71037149 G>A maps to NM_032682.4 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:71102858 G>T maps to NM_032682.4 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr3:71101728 G>A maps to NM_032682.4 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:71021827 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr3:71021827 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr3:71026114 G>A maps to NM_032682.4 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr7:114304339 G>T maps to NM_148898.3 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:114299625 G>C did not map to a codon.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr7:114270014 A>G maps to NM_148898.3 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr7:114270014 A>G maps to NM_148898.3 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:49107795 C>G did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:49113895 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:41555232 C>G maps to NM_001012426.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr6:1313342 C>A maps to NM_033260.3 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:1313373 C>T maps to NM_033260.3 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr6:1313319 C>G maps to NM_033260.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr6:1313562 C>G maps to NM_033260.3 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr6:1313430 C>A maps to NM_033260.3 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr6:1313519 G>A maps to NM_033260.3 W194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr6:1313385 C>T maps to NM_033260.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr11:118850378 G>A did not map to a codon.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr23:55651070 T>G did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:55651014 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr23:55650513 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr23:55651071 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr23:55650326 G>A did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:126139116 C>T maps to NM_017547.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:126142910 G>A maps to NM_017547.3 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr11:126145303 C>T maps to NM_017547.3 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr11:126141491 G>A maps to NM_017547.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:36894042 C>T maps to NM_001102371.1 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr22:36892167 G>A maps to NM_001102371.1 H490H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr22:36894042 C>T maps to NM_001102371.1 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr20:30432976 G>A maps to NM_004118.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr1:74671392 C>T maps to NM_003838.3 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr1:74671226 C>A maps to NM_003838.3 S499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:74670825 T>C maps to NM_003838.3 Y365Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:74670980 C>G maps to NM_003838.3 S417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:52249917 G>A maps to NM_002029.3 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr19:52272426 G>A maps to NM_001005738.1 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr19:52272666 C>T maps to NM_001005738.1 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr10:95454652 G>A maps to NM_145246.4 Y87Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr4:79258927 C>T maps to NM_025074.6 S793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr4:79399117 C>T maps to NM_025074.6 I2667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:79430000 C>T maps to NM_025074.6 P3207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:79430150 C>T maps to NM_025074.6 V3257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr4:79461792 C>T maps to NM_025074.6 R3852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr4:79238533 C>G maps to NM_025074.6 S611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr4:79294004 C>G maps to NM_025074.6 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:79393413 G>A maps to NM_025074.6 T2484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr4:79430063 C>T maps to NM_025074.6 F3228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr4:79173676 C>T maps to NM_025074.6 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:79462136 G>A maps to NM_025074.6 V3966V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr4:79308852 C>T maps to NM_025074.6 Q1325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr4:79258945 C>T maps to NM_025074.6 F799F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr4:79385268 C>T maps to NM_025074.6 F2286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr4:79284665 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr4:79434692 G>A maps to NM_025074.6 L3387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr9:14759862 C>T maps to ENST00000380880 Q1750Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr9:14842623 G>C maps to ENST00000380880 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:14824957 G>A maps to ENST00000380880 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr9:14746433 C>T maps to ENST00000380880 W2060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:14750251 A>G maps to ENST00000380880 N1813N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:14812837 G>T maps to ENST00000380880 I958I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:14859370 G>A maps to ENST00000380880 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr9:14857747 C>G did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr9:14746391 C>T maps to ENST00000380880 Q2074Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:14805088 C>T maps to ENST00000380880 L1115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr9:14784510 G>A maps to ENST00000380880 I1436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr9:14863873 C>A maps to ENST00000380880 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr9:14801752 G>A maps to ENST00000380880 I1200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr9:14801791 C>T maps to ENST00000380880 L1187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr9:14806701 G>A maps to ENST00000380880 L1080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr13:39425117 C>T maps to NM_207361.4 D2205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr13:39446911 C>T maps to NM_207361.4 R2673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr13:39438669 G>A maps to NM_207361.4 W2637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr13:39263355 C>T maps to NM_207361.4 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:39433624 C>T maps to NM_207361.4 Q2473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr13:39262551 C>T maps to NM_207361.4 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr13:39262633 C>T maps to NM_207361.4 Q385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr13:39357306 G>A maps to NM_207361.4 L1914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr13:39261678 C>T maps to NM_207361.4 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr13:39266580 G>A maps to NM_207361.4 V1700V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr13:39265348 A>T maps to NM_207361.4 K1290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr13:39262551 C>T maps to NM_207361.4 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr13:39266034 C>G maps to NM_207361.4 V1518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr4:190862214 C>A maps to NM_004477.2 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr4:190884259 G>A maps to NM_004477.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr4:190876260 A>G maps to NM_004477.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr10:135438790 G>A maps to ENST00000443774 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr6:168475967 C>T maps to NM_024919.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr6:168467490 G>A maps to NM_024919.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr9:85913688 G>T maps to NM_174938.4 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr10:13782238 G>A maps to NM_018027.3 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:13708120 G>A maps to NM_018027.3 Q527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr10:13699485 G>A maps to NM_018027.3 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr10:13789761 C>T maps to NM_018027.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:13702440 G>A maps to NM_018027.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr3:69246183 G>C maps to NM_015123.1 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr15:44180389 C>T maps to NM_032892.3 E289E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr15:44166358 C>T maps to NM_032892.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr14:52187054 C>G maps to ENST00000344768 S436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr23:131233526 C>T did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr23:131234649 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr23:131212673 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:131212725 C>T did not map to a codon.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr11:65156901 C>G maps to NM_031904.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr9:37746198 C>T maps to NM_014907.2 T1390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr9:37746459 C>T maps to NM_014907.2 I1477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:37745631 C>T maps to NM_014907.2 F1201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr9:37708478 C>A maps to NM_014907.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr9:37745772 C>G maps to NM_014907.2 V1248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr9:37746351 G>A maps to NM_014907.2 G1441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:37745550 A>T maps to NM_014907.2 P1174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr9:37735727 C>T maps to NM_014907.2 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr9:37740459 G>A maps to NM_014907.2 E645E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr10:49440293 G>A maps to NM_001018071.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr10:49400846 G>C maps to NM_001018071.3 S682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr10:49376697 G>A maps to NM_001018071.3 V1159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr10:49452883 G>C maps to NM_001018071.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr10:49414969 G>A maps to NM_001018071.3 Q540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr23:12736509 C>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:12516859 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr23:12736322 C>G did not map to a codon.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr23:12516883 G>A did not map to a codon.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr23:12734894 C>T did not map to a codon.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr23:12725659 A>T did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:12724948 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr23:12736409 C>T did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:12736676 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:12712482 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:12735696 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:12736041 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr23:12734517 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:12736649 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:100177719 C>T did not map to a codon.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr12:69968167 C>T maps to NM_006654.3 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr6:41740659 G>A maps to NM_006653.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr13:32757158 A>G maps to NM_023037.2 E1014E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr13:32729675 C>T maps to NM_023037.2 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:32709060 C>T maps to NM_023037.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr13:32745307 G>A maps to NM_023037.2 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr13:32808827 C>A maps to NM_023037.2 S1882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr13:32826016 G>A maps to NM_023037.2 K2391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr13:32812067 C>T maps to NM_023037.2 F2121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr13:32835904 C>G maps to NM_023037.2 S2523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr13:32752543 C>G maps to NM_023037.2 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr13:32745268 C>T maps to NM_023037.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr13:32759285 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr13:32783173 G>C maps to NM_023037.2 L1401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr13:32802652 C>G maps to NM_023037.2 S1756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr13:32709247 C>G maps to NM_023037.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr13:32813912 G>A maps to NM_023037.2 T2194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr13:32868659 G>A maps to NM_023037.2 L2912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr13:32828504 C>T maps to NM_023037.2 L2464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr13:32705944 G>T maps to NM_023037.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr4:48622717 G>A maps to NM_015030.1 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:48605372 C>T maps to NM_015030.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr4:48578163 C>A maps to NM_015030.1 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:48517100 C>T maps to NM_015030.1 L2627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr4:48636379 G>A maps to NM_015030.1 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr4:48549696 G>A maps to NM_015030.1 R1660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr4:48588675 G>A maps to NM_015030.1 D570D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr4:48501603 C>T maps to NM_015030.1 Q2959Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:44974069 G>A maps to NM_032135.3 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr14:44975241 G>A maps to NM_032135.3 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr14:44975862 C>A maps to NM_032135.3 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr7:5633094 C>G maps to ENST00000340250 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr7:5633178 G>A maps to ENST00000340250 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:5645020 C>T maps to ENST00000340250 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:79503669 C>G maps to NM_001077182.2 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr7:127238524 C>T maps to NM_020369.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr7:127238538 G>A maps to NM_020369.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr19:4310510 G>A maps to NM_024333.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr19:4305962 C>T maps to NM_024333.2 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr19:4305977 G>A maps to NM_024333.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:4323175 C>G maps to NM_024333.2 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr15:83438619 G>C maps to NM_001007122.2 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr2:49190072 A>G maps to NM_000145.3 F629F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:49244634 G>A maps to NM_000145.3 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr2:49189907 G>A maps to NM_000145.3 Y684Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr2:49190753 G>T maps to NM_000145.3 C402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:49190702 T>G maps to NM_000145.3 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:49195961 C>T maps to NM_000145.3 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr2:49189931 G>A maps to NM_000145.3 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr15:39910415 G>A maps to NM_152597.4 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:186671525 C>T maps to NM_173651.2 L5920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:186671135 G>A maps to NM_173651.2 S5790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:186673739 G>C maps to NM_173651.2 L6658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr2:186697845 G>T maps to NM_173651.2 G6962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr2:186673330 C>G maps to NM_173651.2 S6522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr5:52778833 G>A maps to NM_013409.1 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr5:52778768 G>T maps to NM_013409.1 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:120128497 G>A maps to NM_007085.4 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr3:120121765 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:677927 G>A maps to NM_005860.2 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:677930 C>T maps to NM_005860.2 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr19:677930 C>T maps to NM_005860.2 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr5:132569151 G>A maps to NM_015082.1 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr5:132552956 G>T maps to NM_015082.1 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr4:162463735 C>T maps to NM_020116.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr4:162577545 C>G maps to NM_020116.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr4:162697122 G>A maps to NM_020116.3 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr4:162463735 C>T maps to NM_020116.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr4:162463812 G>A maps to NM_020116.3 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr21:47570312 G>A maps to ENST00000397748 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr21:47571573 C>T maps to ENST00000397748 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr11:61732221 C>A maps to NM_002032.2 G177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr11:61732364 T>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr23:31089857 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr23:31089911 G>T did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:31089731 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr23:31089817 C>A did not map to a codon.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr16:53967949 G>A maps to NM_001080432.2 R431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr16:53913759 C>G maps to NM_001080432.2 S327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:48340026 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr7:2275053 T>A maps to NM_013393.1 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr7:2275017 T>G maps to NM_013393.1 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr17:61904235 C>T maps to NM_017647.3 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr17:61898903 G>A maps to NM_017647.3 Q566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr17:61904003 C>T maps to NM_017647.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr17:61897623 C>T maps to NM_017647.3 K749K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr17:61901257 C>T maps to NM_017647.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr17:61901284 C>T maps to NM_017647.3 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr17:61902631 C>A maps to NM_017647.3 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr17:61904000 G>T maps to NM_017647.3 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:71318494 A>C maps to NM_018348.5 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:71319745 A>T maps to NM_018348.5 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr16:71318283 C>A maps to NM_018348.5 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:37426533 C>T maps to NM_015050.2 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr6:37429338 G>A maps to NM_015050.2 E370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:78444568 C>T maps to ENST00000436586 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr9:133470930 C>G maps to NM_003934.1 S49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr9:133499064 G>T maps to NM_003934.1 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr9:133506165 G>A maps to NM_003934.1 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr9:133499073 C>T maps to NM_003934.1 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr6:143825327 C>T maps to NM_032020.4 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr16:70499066 C>T maps to NM_145059.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr16:70504274 C>G maps to NM_145059.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:70506487 C>T maps to NM_145059.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr16:70513197 C>T maps to NM_145059.2 H1015H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr16:70508128 G>A maps to NM_145059.2 R625R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr23:44401283 T>C did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr23:154282926 C>A did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr15:91421500 C>T maps to NM_002569.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr15:91424196 C>T maps to NM_002569.2 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr15:91424882 C>A maps to NM_002569.2 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr15:91424678 G>A maps to NM_002569.2 Q652Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr15:91423193 C>T maps to NM_002569.2 I452I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr15:91423992 C>G maps to NM_002569.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:31195650 C>T maps to NM_004960.3 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr16:31195260 C>A maps to NM_004960.3 Y91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr16:31201393 C>A maps to NM_004960.3 S367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:31195545 C>T maps to NM_004960.3 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr16:31195650 C>T maps to NM_004960.3 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr19:49253608 G>A maps to NM_000148.3 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:49254223 G>A maps to NM_000148.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr19:49254076 G>A maps to NM_000148.3 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:33310998 C>T maps to ENST00000380081 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr8:33246681 G>A maps to ENST00000380081 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:49207214 C>T maps to NM_001097638.2 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr11:94278768 G>C maps to NM_002033.3 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr11:94278564 C>T maps to NM_002033.3 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:5866612 C>G maps to NM_002034.2 *375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr19:5866612 C>G maps to NM_002034.2 *375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr14:66136029 C>T maps to NM_178155.1 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr6:96651576 G>A maps to NM_006581.3 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:96651987 G>A maps to NM_006581.3 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr19:50311870 C>T maps to NM_025129.4 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:50315534 T>C maps to NM_025129.4 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr11:6503022 G>T maps to NM_012192.3 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr3:180693956 C>T maps to NM_005087.3 N581N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:180630520 C>T maps to NM_005087.3 Y16Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:180675668 C>T maps to NM_005087.3 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr3:180675619 A>G maps to NM_005087.3 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr17:7507214 G>A maps to NM_004860.3 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:35632063 C>T maps to NM_005031.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr19:35632084 C>T maps to NM_005031.3 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr19:35657214 C>T maps to NM_001164605.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:35657166 C>G maps to NM_001164605.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr5:39202999 G>A maps to ENST00000263405 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr5:39202486 G>C maps to ENST00000263405 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr3:46000913 G>A maps to NM_024513.2 F1186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:46008454 G>A maps to NM_024513.2 Q791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr3:46008896 C>T maps to NM_024513.2 Q643Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr3:46001007 G>C maps to NM_024513.2 S1155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr3:46008020 G>A maps to NM_024513.2 D935D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr3:46007804 C>G maps to NM_024513.2 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr3:46010024 G>A maps to NM_024513.2 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr6:111983076 G>A maps to NM_153047.1 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr6:112041146 A>C maps to NM_153047.1 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr3:197476898 G>A maps to NM_032288.6 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr7:90894809 C>T maps to NM_003505.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr7:90895307 C>T maps to NM_003505.1 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr7:90894815 C>T maps to NM_003505.1 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:90895016 C>T maps to NM_003505.1 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:90894809 C>T maps to NM_003505.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:90895664 C>T maps to NM_003505.1 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr7:90894908 G>T maps to NM_003505.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr7:90895379 G>A maps to NM_003505.1 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr7:90896135 C>T maps to NM_003505.1 V647V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr12:130648350 C>T maps to NM_007197.3 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr12:130648299 C>A maps to NM_007197.3 C271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr12:130648383 C>T maps to NM_007197.3 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr17:42635139 G>A maps to NM_001466.3 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr17:42636720 C>T maps to NM_001466.3 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr17:42636534 G>A maps to NM_001466.3 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr17:42636591 G>A maps to NM_001466.3 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr8:28378297 G>A maps to NM_017412.3 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr2:208633055 G>A maps to NM_003468.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr2:208633391 C>T maps to NM_003468.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr2:202900668 C>T maps to NM_003507.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:202899543 G>C maps to NM_003507.1 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr2:202900170 G>A maps to NM_003507.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:202900974 G>A maps to NM_003507.1 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr10:35928770 C>T maps to NM_031866.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr10:35928821 C>T maps to NM_031866.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr7:72848450 G>A maps to NM_003508.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr7:72850004 C>T maps to NM_003508.2 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:72849818 G>A maps to NM_003508.2 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr19:3526166 C>G maps to NM_001136198.1 S82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr19:3531969 G>A maps to NM_001136198.1 Q295Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr14:31066666 A>G maps to NM_017769.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr14:31074777 A>T maps to NM_017769.3 K360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr14:31071316 C>T maps to NM_017769.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr5:151179851 C>T maps to NM_198395.1 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr4:76582809 G>A maps to NM_203505.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr4:76580327 C>T maps to NM_203505.2 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr17:41063349 C>T maps to NM_000151.2 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr2:169764144 G>A maps to NM_021176.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr17:42148545 C>T maps to NM_138387.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr17:42152678 C>G maps to NM_138387.3 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr17:42148506 C>T maps to NM_138387.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr23:153760416 G>C did not map to a codon.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr23:153763387 G>T did not map to a codon.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr23:153761168 C>G did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr23:153762289 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr17:78084816 C>T maps to NM_001079804.1 Y543Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr17:78079574 G>T maps to NM_001079804.1 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr17:78078669 C>T maps to NM_001079804.1 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr4:144390254 G>A maps to NM_207123.2 K696K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr4:144359595 G>A maps to NM_207123.2 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr23:153940812 G>A did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr23:153944441 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr22:17472958 G>T maps to NM_001037814.1 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr22:17449259 C>T maps to NM_001037814.1 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:17472816 C>A maps to NM_001037814.1 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr22:17468985 G>A maps to NM_001037814.1 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr22:17472910 G>A maps to NM_001037814.1 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr22:17443703 C>T maps to NM_001037814.1 K548K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr17:7144968 C>G maps to NM_007278.1 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr16:75601961 C>T maps to NM_007285.6 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr6:29588976 G>A maps to NM_001470.2 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr6:29576386 G>A maps to NM_001470.2 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr6:29572738 G>T maps to NM_001470.2 V822V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:29577036 G>A maps to NM_001470.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr6:29589916 G>A maps to NM_001470.2 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr6:29572648 G>C maps to NM_001470.2 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr9:101068555 G>A maps to NM_005458.7 I692I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:101125089 G>A maps to NM_005458.7 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:27117527 G>T maps to NM_002040.3 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr21:27137083 C>T maps to NM_002040.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:50570912 G>C maps to NM_005254.5 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:151063030 C>T maps to NM_144618.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:151065681 G>T maps to NM_144618.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr1:151070407 C>T maps to NM_144618.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr5:161300199 C>T maps to NM_001127648.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr5:161322861 G>C maps to NM_001127648.1 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr5:161324340 G>A maps to NM_001127648.1 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:46390672 G>A maps to ENST00000507069 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:46388148 C>T maps to ENST00000507069 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:151358367 C>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:151366204 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr23:151424300 G>T did not map to a codon.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr23:151424260 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:151424362 G>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:151366255 T>C did not map to a codon.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr4:46979076 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:46973160 C>T maps to NM_000809.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr4:46979647 C>A did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr4:46930376 A>C maps to NM_000809.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr15:27126076 G>A maps to NM_000810.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr5:161113292 C>G maps to NM_000811.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr5:161119110 C>T maps to NM_000811.2 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr5:161128776 T>A maps to NM_000811.2 *454K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr5:161119154 C>G maps to NM_000811.2 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr4:47427923 C>G maps to NM_000812.3 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr4:47033933 C>T maps to NM_000812.3 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr4:47163453 G>T maps to NM_000812.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:47163396 G>A maps to NM_000812.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr4:47427751 C>A maps to NM_000812.3 S381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr4:47427857 C>T maps to NM_000812.3 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr4:47405720 C>A maps to NM_000812.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr5:160721254 G>A maps to NM_021911.2 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:160761888 G>T maps to NM_021911.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:160753386 G>A maps to NM_021911.2 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr5:160972280 C>T maps to NM_021911.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr15:26792967 A>T maps to NM_021912.4 L465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr15:26866498 G>T maps to NM_021912.4 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr1:1956491 A>G maps to NM_000815.4 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr1:1961618 C>G maps to NM_000815.4 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr23:151123199 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:151124308 A>G did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr23:151138850 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr23:151129819 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr23:151138713 G>A did not map to a codon.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr23:151124029 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:151124034 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr23:151129826 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr4:46043249 C>A maps to NM_173536.3 G385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr5:161528315 C>T maps to NM_198903.2 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr5:161580367 C>A maps to NM_198903.2 Y514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr5:161580265 G>C maps to NM_198903.2 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr15:27777981 C>T maps to NM_033223.4 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:27725812 G>T maps to NM_033223.4 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr15:27271919 C>T maps to NM_033223.4 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr15:27772696 C>T maps to NM_033223.4 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:170222426 C>G maps to NM_014211.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr23:151821060 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr23:151821097 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr23:151818287 C>A did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:151808854 G>A did not map to a codon.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr23:151818269 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr23:151821356 G>C did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:151806688 G>A did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr6:89981379 C>A maps to NM_002043.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:89974214 G>A maps to NM_002043.2 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:89978824 G>A maps to NM_002043.2 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr3:97744435 A>G maps to NM_001105580.1 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:97744471 C>T maps to NM_001105580.1 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr2:171700563 T>A maps to NM_000817.2 Y216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr2:171710423 C>G maps to NM_000817.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr10:26581832 T>C maps to NM_001134366.1 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr10:26559630 C>A maps to NM_001134366.1 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr10:26513551 G>A maps to NM_001134366.1 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr10:26558050 G>T maps to NM_001134366.1 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr10:26534902 C>T maps to NM_001134366.1 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr10:26581455 C>T maps to NM_001134366.1 N483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr10:26512835 C>T maps to NM_001134366.1 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr1:68152113 C>G maps to NM_001924.3 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:92220695 C>T maps to NM_006705.3 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:13065318 G>A maps to NM_052850.2 C124C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:49355830 C>A did not map to a codon.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr23:49355892 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr23:49355892 C>G did not map to a codon.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr4:843556 C>T maps to NM_005255.2 A1280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr4:875738 G>A maps to NM_005255.2 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:887188 C>T maps to NM_005255.2 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr4:845580 C>T maps to NM_005255.2 V1155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr4:861047 C>T maps to NM_005255.2 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr4:875822 C>G maps to NM_005255.2 G511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr4:844869 G>A maps to NM_005255.2 Q1171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr4:853436 C>T maps to NM_005255.2 P1080P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:65812871 G>A maps to NM_033036.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr14:88450814 G>A maps to NM_000153.2 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr14:88459415 C>T maps to NM_000153.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr14:88459325 G>A maps to NM_000153.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr14:88411994 G>A maps to NM_000153.2 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:24124666 C>T maps to NM_001008216.1 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:24125176 C>T maps to NM_001008216.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:73759153 G>A maps to ENST00000437911 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:73759141 G>A maps to ENST00000437911 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr15:49575788 G>A maps to NM_002044.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr15:49531512 C>G maps to NM_002044.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:38956809 G>A maps to NM_138801.2 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:38893362 G>A maps to NM_138801.2 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:38960688 C>T maps to NM_138801.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr2:38908552 C>T maps to NM_138801.2 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr18:33267147 C>G maps to NM_020474.3 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:151802336 G>A maps to NM_022087.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr7:151802369 C>A maps to NM_022087.2 Y209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr7:151791434 C>T maps to NM_022087.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr7:151818671 G>A maps to NM_022087.2 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr9:101608350 C>T maps to NM_024642.3 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr9:101606466 C>G maps to NM_024642.3 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr2:155098557 C>G maps to NM_052917.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr1:230391012 G>A maps to NM_004481.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:230415080 G>C maps to NM_004481.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:166627185 T>A maps to NM_004482.3 K9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr2:166621535 A>G maps to NM_004482.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr12:89917930 C>T maps to NM_003774.4 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr12:89917870 G>A maps to NM_003774.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr12:51757939 C>T maps to NM_007210.3 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:51759232 G>A maps to NM_007210.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:51759226 G>A maps to NM_007210.3 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:174239625 G>A maps to NM_017423.2 Q584Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr4:174235264 G>T maps to NM_017423.2 E516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr12:4853707 G>A maps to NM_017417.1 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr12:4835914 C>G maps to NM_017417.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr12:4830022 C>G maps to NM_017417.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr12:4855393 T>C maps to NM_017417.1 Y381Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr12:4854666 T>G maps to NM_017417.1 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr12:4835935 C>T maps to NM_017417.1 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr12:4881657 G>A maps to NM_017417.1 K603K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr12:132688235 C>A did not map to a codon.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr14:69814712 C>G maps to NM_020692.2 G511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr3:16217180 G>T maps to NM_054110.4 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr3:16250071 C>A maps to NM_054110.4 S325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr3:16254233 C>T maps to NM_054110.4 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr11:11394085 G>A maps to NM_198516.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr11:11362440 G>A maps to NM_198516.2 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr7:151664462 A>C maps to NM_145292.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr7:151711862 G>A maps to NM_145292.3 W387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr4:172735739 G>A maps to NM_001034845.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr4:173269793 G>A maps to NM_001034845.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:173734757 C>T maps to NM_001034845.2 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr4:172735775 C>T maps to NM_001034845.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:56688512 C>T maps to NM_033106.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr19:56688515 C>T maps to NM_033106.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr18:74962761 C>G maps to NM_001480.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr18:74980671 C>T maps to NM_001480.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:74073115 C>T maps to NM_003857.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr17:74071074 C>T maps to NM_003857.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr17:74071056 C>T maps to NM_003857.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr17:74073145 C>T maps to NM_003857.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr17:74071065 C>T maps to NM_003857.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:81411162 C>T maps to NM_022041.3 Q586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr16:81391456 C>G maps to NM_022041.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr11:62393545 G>A maps to NM_198335.2 Q928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr11:62393546 G>A maps to NM_198335.2 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr11:62393904 T>A maps to NM_198335.2 G864G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr11:62398116 G>A maps to NM_198335.2 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr11:62398081 C>T maps to NM_198335.2 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr11:62400084 G>A maps to NM_198335.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr11:62407193 C>G maps to NM_198335.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr11:62396346 G>A maps to NM_198335.2 Q714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:62397102 G>C maps to NM_198335.2 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr15:42568596 C>T maps to NM_198141.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr15:42613981 G>A did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr15:42632056 A>G maps to NM_198141.2 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr15:42602934 C>G maps to NM_198141.2 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr15:42631963 C>G maps to NM_198141.2 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:115395212 T>C maps to NM_001130064.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr12:6645749 C>G maps to NM_002046.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr12:6647114 T>C maps to NM_002046.3 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr19:36033256 G>C maps to NM_014364.4 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr5:57790588 G>T maps to NM_152687.2 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:128109129 C>T maps to NM_015635.2 Q1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr9:128065098 G>C maps to NM_015635.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr9:130027209 G>A maps to NM_032293.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:130027209 G>A maps to NM_032293.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:130083017 G>A maps to NM_032293.4 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr7:30662009 G>A maps to NM_002047.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:30651838 C>T maps to NM_002047.2 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr21:34876553 T>G maps to NM_001136006.1 A970A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:29706990 G>A maps to NM_152237.1 *338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr22:29704253 G>C maps to NM_152236.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr22:29708036 G>A maps to NM_152236.1 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr22:29708183 G>A maps to NM_152236.1 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr17:34073363 G>C maps to NM_139285.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr17:34071980 C>T maps to NM_139285.2 E845E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr17:34073006 G>T maps to NM_139285.2 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr17:34079686 C>T maps to NM_139285.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr17:34077329 C>T maps to NM_139285.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:34073060 G>A maps to NM_139285.2 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:34076185 G>C maps to NM_139285.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr17:34077314 C>T maps to NM_139285.2 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr17:34072351 G>A maps to NM_139285.2 Q722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:101017393 C>T maps to NM_174942.1 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr13:114523971 C>T maps to ENST00000357389 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:90106742 C>T maps to NM_001481.2 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr16:90109650 C>T maps to NM_001481.2 F445F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-UY-A9PB-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:48652248 G>T did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:48650255 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:48650376 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:48650545 C>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:48650589 C>T did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr23:48652417 C>G did not map to a codon.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr23:48650332 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr23:48650369 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:128199903 G>A maps to NM_032638.4 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr10:8115823 G>C maps to NM_001002295.1 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr10:8106046 C>T maps to NM_001002295.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr10:8100727 C>T maps to NM_001002295.1 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr10:8100268 G>T maps to NM_001002295.1 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:8100478 C>T maps to NM_001002295.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr8:11615911 G>A maps to NM_002052.3 Q419Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr20:61041538 C>T maps to NM_080473.4 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr20:61039960 G>A maps to NM_080473.4 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:19612020 G>A maps to ENST00000404158 K452K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr19:19613327 C>A maps to ENST00000404158 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr19:19606976 C>T maps to ENST00000404158 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:19612806 C>T maps to ENST00000404158 F530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr19:19609397 G>A maps to ENST00000404158 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr19:19606910 C>T maps to ENST00000404158 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr1:153782754 G>A maps to NM_020699.2 I560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:120884566 C>T maps to NM_176818.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:99821276 T>A maps to NM_178831.6 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WY-01A-11D-A22Z-08 chr22:30685447 C>G maps to NM_001037666.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr22:30682065 C>T maps to ENST00000434291 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:155207266 C>A maps to NM_001005742.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr9:35748497 C>T maps to NM_020944.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr4:22749627 T>A maps to NM_020973.3 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr4:22749054 C>T maps to NM_020973.3 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:81810575 G>C maps to ENST00000264326 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr10:104142017 C>T maps to NM_004193.2 I1835I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr10:104128190 G>A maps to NM_004193.2 Q952Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr1:89523876 G>C maps to NM_002053.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr1:89522717 G>C maps to NM_002053.2 S325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:89579941 G>A maps to NM_004120.3 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr1:89579890 C>T maps to NM_004120.3 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr1:89474710 C>T maps to NM_018284.2 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:89477537 G>A maps to NM_018284.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:89654465 C>T maps to NM_052941.4 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:89729418 C>T maps to NM_052942.3 Q454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:89735196 G>A maps to NM_052942.3 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:89735132 G>A maps to NM_052942.3 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr1:89845981 G>A maps to NM_198460.2 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:89834215 C>T maps to NM_198460.2 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:89844164 G>C maps to NM_198460.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr1:89618085 C>A maps to NM_207398.2 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr1:89637585 C>A maps to NM_207398.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr7:150845676 C>T maps to NM_001098834.1 *364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr7:150845867 G>A maps to NM_001098834.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:237075027 C>T maps to NM_001485.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr2:237075027 C>T maps to NM_001485.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr2:237074741 C>A maps to NM_001485.2 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr4:72622631 C>T did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr4:72629559 G>T maps to ENST00000504199 C208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr2:163204190 C>A maps to NM_012198.3 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:163213344 C>T maps to NM_012198.3 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:127223116 G>A maps to NM_024523.5 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr2:109091989 G>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr2:109092218 G>T maps to NM_181453.3 V991V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr2:109109089 C>T maps to NM_181453.3 Q1431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr2:109098271 G>A maps to NM_181453.3 Q1060Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr2:109086466 C>T maps to NM_181453.3 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:109087477 C>T maps to NM_181453.3 Q565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr19:13007148 C>T maps to NM_000159.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WY-01A-11D-A22Z-08 chr19:13002714 C>T maps to NM_000159.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr19:13007761 C>T maps to NM_000159.2 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr19:13007117 C>T maps to NM_000159.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:111849350 C>T maps to NM_001190259.1 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:111851949 C>T maps to NM_001190259.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr21:34142131 T>G maps to NM_016631.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr2:163003993 G>A maps to ENST00000233604 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr14:55310581 G>C maps to NM_001024070.1 S211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr14:55310785 G>A maps to NM_001024024.1 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr15:41056392 C>T maps to NM_005258.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr15:41056395 C>T maps to NM_005258.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr7:44190671 G>A maps to NM_000162.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:44193017 C>T maps to NM_000162.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:44192942 C>T maps to NM_000162.3 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:44193017 C>A maps to NM_000162.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr7:44187337 G>A maps to NM_000162.3 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr7:44186204 G>C maps to NM_000162.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr7:44186117 G>T maps to NM_000162.3 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr2:27731063 C>T maps to NM_001486.3 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr2:27730582 G>C maps to NM_001486.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:27728698 C>T maps to NM_001486.3 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr2:27745371 C>T maps to NM_001486.3 R540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:27746155 G>A maps to NM_001486.3 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:27746143 C>G maps to NM_001486.3 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:27730126 C>A maps to NM_001486.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr6:53370195 C>A maps to NM_001498.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr6:53372389 G>A maps to NM_001498.3 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr6:53379249 G>A maps to NM_001498.3 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:94370096 G>A maps to NM_002061.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr6:10874770 G>A maps to NM_004752.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:10874872 A>G maps to NM_004752.3 Y292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr6:10874963 G>C maps to NM_004752.3 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:10876752 C>T maps to NM_004752.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr12:120574331 C>A maps to NM_006836.1 E2328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:120575012 C>T maps to NM_006836.1 K2258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:120586010 G>A maps to NM_006836.1 L1562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:120591102 G>A maps to NM_006836.1 L1326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:120591171 G>A maps to NM_006836.1 L1303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr12:120565653 C>T maps to NM_006836.1 *2672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr12:120572125 G>C maps to NM_006836.1 S2429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:120569003 A>G maps to NM_006836.1 S2516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr12:120587839 G>C maps to NM_006836.1 L1439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:120582451 A>G maps to NM_006836.1 C1781C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:79118370 C>A maps to NM_001097636.1 Y358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr6:10556715 C>T maps to NM_001491.2 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr6:10621626 C>T maps to NM_145649.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr6:10586312 A>T maps to NM_145655.3 K31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr6:10529482 C>T maps to NM_145649.4 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr6:10626776 G>A maps to NM_145649.4 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:59910808 G>A maps to NM_004751.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:59911183 G>A maps to NM_004751.2 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr15:59911492 C>G maps to NM_004751.2 Y352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:74324902 G>A maps to NM_016591.2 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr5:74325124 G>C maps to NM_016591.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr15:57917988 C>T maps to NM_001018090.3 Q142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr15:57913882 C>T maps to NM_001018090.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr16:81116534 G>C maps to NM_004483.4 S153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr9:74764525 C>T maps to ENST00000238018 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr9:74842884 C>T maps to ENST00000238018 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr9:74863250 C>A maps to ENST00000238018 S453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr9:74842872 C>T maps to ENST00000238018 H279H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr8:75262800 C>T maps to NM_018972.2 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr8:75272519 G>T maps to NM_018972.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:118455279 C>T maps to NM_017686.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr1:118455249 G>A maps to NM_017686.3 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr16:19522208 T>C maps to NM_016641.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr19:18499743 G>C maps to NM_004864.2 *309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr19:18499552 G>C maps to NM_004864.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:48416477 C>G maps to NM_016204.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr10:48413871 C>T maps to NM_016204.1 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr10:48414501 G>C maps to NM_016204.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr12:7842974 G>A maps to NM_020634.1 F198F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-E5-A2PC-01A-11D-A202-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-FD-A3SJ-01A-12D-A22Z-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-FD-A5BX-01A-11D-A26M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr20:34025207 G>A maps to NM_000557.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr8:97156883 C>T maps to NM_001001557.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr8:97156940 C>T maps to NM_001001557.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr2:20871010 C>T maps to NM_182828.2 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr2:20870914 C>T maps to NM_182828.2 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr5:132198222 T>C maps to NM_005260.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:132197955 A>G maps to NM_005260.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:153670976 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr23:153665606 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr23:153668395 C>T did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr23:153670013 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:5810188 G>C maps to NM_001494.3 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr10:5810193 G>A maps to NM_001494.3 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr10:5808245 G>A maps to NM_001494.3 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr5:37816163 C>T maps to NM_001190468.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:57298050 G>A maps to NM_182569.3 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr23:69647193 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr23:69646847 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:69646311 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr23:69649384 C>T did not map to a codon.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr23:69649375 G>C did not map to a codon.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr23:69652258 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:69649411 C>A did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr16:30123467 C>T maps to NM_024307.2 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr16:30119559 G>A maps to NM_024307.2 R265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr11:76940220 A>G maps to ENST00000376217 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr11:76944072 G>A maps to ENST00000376217 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr11:76944075 G>A maps to ENST00000376217 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr11:76982211 C>T maps to ENST00000376217 W121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:76944217 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr11:75160075 C>T maps to NM_030792.6 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr11:75168776 C>T maps to NM_030792.6 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr12:58009630 G>T maps to NM_001111270.1 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr12:58006800 C>T maps to NM_001111270.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr12:58006839 C>T maps to NM_001111270.1 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr17:650820 G>A maps to NM_015721.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr17:650112 C>T maps to NM_015721.2 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr17:649461 G>C maps to NM_015721.2 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr5:154267889 G>T maps to NM_015465.3 L1469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:154308187 C>T maps to NM_015465.3 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:154272067 C>T maps to NM_015465.3 L1213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr5:154308190 C>T maps to NM_015465.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr5:154296708 C>T maps to NM_015465.3 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr5:154307067 C>T maps to NM_015465.3 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr5:154292598 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr2:39008787 C>T maps to NM_024775.9 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr19:45593707 T>C maps to NM_024707.2 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:14038305 C>G did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:14027075 G>T did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr23:14038305 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr23:14027260 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:17959298 T>C maps to NM_001130009.1 V411V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-A3WW-01A-22D-A23M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr17:42988716 G>A maps to NM_002055.3 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:42992743 G>C maps to NM_002055.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:92941705 G>A maps to NM_005263.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:92946169 G>A maps to NM_005263.3 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:135865145 C>T maps to NM_004188.4 C222C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:158384152 G>T maps to ENST00000264263 E546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:158383144 C>A maps to ENST00000264263 S486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr3:158364637 C>A maps to ENST00000264263 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr3:158369973 C>G maps to ENST00000264263 S279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:74018259 G>A maps to NM_032380.3 Q719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr5:74035893 C>G maps to NM_032380.3 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr6:13487044 G>A maps to NM_018988.2 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr6:13365751 C>T maps to NM_018988.2 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr16:67709543 G>A maps to NM_030819.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr16:67709744 C>T maps to NM_030819.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr16:67709390 C>G maps to NM_030819.3 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:67709504 C>T maps to NM_030819.3 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr16:67709612 G>C maps to NM_030819.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr16:67719480 C>T maps to NM_030819.3 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr2:69575327 C>T maps to ENST00000357308 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:69573054 G>A maps to ENST00000357308 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:179763569 C>T maps to NM_005110.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr5:179743796 A>T maps to NM_005110.2 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr5:179743769 G>A maps to NM_005110.2 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr5:179743975 A>G maps to NM_005110.2 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr10:117823914 T>A maps to NM_005264.4 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr5:137593629 G>C maps to NM_001496.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr6:55216286 G>T maps to NM_207410.2 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:23481469 G>A maps to NM_015044.4 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr17:73235615 G>A maps to NM_138619.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:73240752 C>A maps to NM_138619.2 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr17:73238530 C>T maps to NM_138619.2 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:73235513 C>T maps to NM_138619.2 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:30536734 G>A maps to NM_024051.3 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr7:30538493 T>C maps to NM_024051.3 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:30538451 G>A maps to NM_024051.3 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr2:85785669 C>T maps to NM_000821.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:85778162 C>T maps to NM_000821.4 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr2:85777173 C>T maps to NM_000821.4 V720V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr2:85779681 T>C maps to NM_000821.4 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:85781344 G>C maps to NM_000821.4 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr8:63938786 C>G maps to NM_003878.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr8:63939793 G>C maps to NM_003878.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr17:34937959 C>T maps to NM_024835.3 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr17:34916670 C>T maps to NM_024835.3 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr1:235505339 G>C maps to NM_001037277.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr1:235506023 G>T maps to NM_001037277.1 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr22:25023890 C>A maps to NM_005265.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:25016335 G>T maps to NM_005265.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:25023472 G>A maps to NM_005265.2 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr22:25011026 C>T maps to NM_005265.2 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr22:25023475 C>A maps to NM_005265.2 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr22:25010754 G>A maps to NM_005265.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr22:24622207 C>T maps to NM_001099781.1 E355E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr20:33433139 G>A maps to NM_178026.2 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr20:33440244 C>T maps to NM_178026.2 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr20:23966390 G>T maps to NM_178311.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:22988877 G>A maps to ENST00000215938 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:61995218 G>A maps to NM_000515.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:61994707 G>A maps to NM_000515.3 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr10:85901273 G>A maps to ENST00000436406 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr10:85909865 C>A maps to ENST00000436406 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr5:42718754 C>T maps to NM_000163.2 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr5:42718964 G>A maps to NM_000163.2 E452E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:31013634 C>T maps to NM_000823.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr7:31018735 G>A maps to NM_000823.3 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:31014104 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:172162970 C>A maps to NM_198407.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr3:172165522 A>T maps to NM_198407.2 C227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:172165774 G>A maps to NM_198407.2 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr3:172165525 G>A maps to NM_198407.2 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr3:172165990 G>A maps to NM_198407.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr3:172165398 G>A maps to NM_004122.2 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr3:172165708 G>A maps to NM_198407.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr11:59611385 G>C maps to NM_005142.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:59611370 G>C maps to NM_005142.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr11:59599269 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:100283074 G>A maps to NM_022574.4 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr7:100280338 C>T maps to NM_022574.4 W825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:100280766 G>C maps to NM_022574.4 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:233651881 T>G maps to ENST00000373566 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr2:233655997 C>A maps to ENST00000373566 S397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr2:233660832 C>G maps to ENST00000373566 S536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr2:233660927 C>T maps to ENST00000373566 Q568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr2:233710440 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr2:233710507 C>G maps to ENST00000373566 L1146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr7:150417211 G>A maps to NM_130759.3 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr7:150417943 C>T maps to NM_130759.3 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:150417148 C>T maps to NM_130759.3 N19N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr7:150417583 T>C maps to NM_130759.3 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr7:150390174 C>T maps to NM_015660.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:150390121 C>T maps to NM_015660.2 Q250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr7:150439442 A>G maps to ENST00000447239 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:150327200 G>C maps to ENST00000438845 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr7:150325267 G>A maps to ENST00000438845 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr7:150164397 C>T maps to NM_175571.2 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr7:150163827 C>G maps to NM_175571.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr7:150171305 A>T maps to NM_175571.2 K297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr7:150174540 G>A maps to NM_175571.2 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:102442446 T>C maps to NM_017676.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:102433154 G>A maps to NM_017676.2 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr5:102432326 C>T maps to NM_017676.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr20:25405845 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr8:41387762 G>T maps to NM_032336.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr8:41397244 G>T maps to NM_032336.2 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:14591575 G>A maps to NM_202470.1 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:78546504 C>T maps to NM_017655.4 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:78511987 C>A maps to NM_017655.4 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr19:3586816 C>T maps to NM_133261.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr19:46172840 G>A maps to NM_000164.2 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:46174546 C>T maps to NM_000164.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr19:46174546 C>T maps to NM_000164.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr19:46173951 G>A maps to NM_000164.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr19:46174546 C>G maps to NM_000164.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:46178077 G>A maps to NM_000164.2 W209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr19:46180988 C>G maps to NM_000164.2 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:46177432 C>T maps to NM_000164.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:27903632 C>T maps to NM_001085454.1 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr17:27904202 G>A maps to NM_001085454.1 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr17:27903236 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:27902475 C>T maps to NM_001085454.1 K622K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr17:27908781 G>A maps to NM_001085454.1 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:110399112 G>C maps to NM_057169.3 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr12:110391019 C>T maps to NM_057169.3 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:110429500 C>G maps to NM_057169.3 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr12:110397700 G>C maps to NM_057169.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:110429506 G>A maps to NM_057169.3 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr13:20717190 C>T maps to NM_021954.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:147230406 G>A maps to NM_005266.5 Q314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr1:147230968 C>T maps to NM_005266.5 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr1:147231262 G>C maps to NM_005266.5 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr1:147230737 C>T maps to NM_005266.5 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr1:147380453 G>A maps to NM_005267.4 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr1:39340563 G>A maps to NM_030772.4 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:70443613 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:35251004 C>G maps to NM_001005752.1 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:35250590 C>T maps to NM_001005752.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:35251032 C>T maps to NM_001005752.1 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr1:35227412 C>T maps to NM_153212.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr1:35227229 C>T maps to NM_153212.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:35227556 C>T maps to NM_153212.2 C234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:35227097 C>T maps to NM_153212.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr1:35227214 G>C maps to NM_153212.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr6:87994303 G>C maps to NM_198568.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr6:87994087 G>A maps to NM_198568.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr1:228346667 C>A maps to NM_020435.2 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:35045101 T>C maps to NM_020660.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr15:35044990 A>G maps to NM_020660.1 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:35894524 C>T maps to NM_153368.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr23:30712534 C>G did not map to a codon.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr23:30695562 G>A did not map to a codon.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr4:80329309 C>A maps to NM_033214.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr3:141905046 C>T maps to NM_001039547.2 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr3:141889248 G>A maps to NM_001039547.2 D453D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr3:141917775 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr9:86414186 G>A maps to NM_025211.3 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr2:69207921 C>T maps to NM_019617.3 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr2:69173520 G>A maps to NM_182536.2 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr2:69172541 C>T maps to NM_182536.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:100653404 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr23:100656703 C>G did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:100653915 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr3:33110347 C>T maps to NM_000404.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr3:33110329 G>A maps to NM_000404.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:134244147 G>T maps to NM_138342.3 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr11:134244527 C>T maps to NM_138342.3 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr11:134243651 G>A maps to NM_138342.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr11:134244909 C>T maps to NM_138342.3 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr11:134183856 C>T maps to NM_001080407.2 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr11:134180463 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr11:134147327 G>A maps to NM_001080407.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr7:8110598 C>A maps to NM_138426.2 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:8062157 C>T maps to NM_138426.2 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:69561006 G>C maps to NM_015554.1 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr9:6550815 G>A maps to NM_000170.2 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr9:6620278 G>A maps to NM_000170.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr9:6602110 G>A maps to NM_000170.2 Q385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:6605253 C>T maps to NM_000170.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr9:6605214 G>A maps to NM_000170.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr9:6605262 G>A maps to NM_000170.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:131267110 G>A maps to NM_001003722.1 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr16:74640923 G>A maps to NM_012201.5 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:74493621 G>A maps to NM_012201.5 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr16:74493621 G>C maps to NM_012201.5 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr16:74537565 C>A maps to NM_012201.5 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr16:74525053 C>A maps to NM_012201.5 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr16:74519763 G>A maps to NM_012201.5 R501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:74506260 G>A maps to NM_012201.5 Q701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr12:57861868 C>T maps to NM_005269.2 D390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr12:57857794 G>A maps to NM_005269.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr12:57864226 C>T maps to NM_005269.2 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:57861985 G>T maps to NM_005269.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr2:121747282 C>T maps to NM_005270.4 Q1265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:121747002 G>C maps to NM_005270.4 L1171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr2:121708920 C>T maps to NM_005270.4 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr2:121744053 G>A maps to NM_005270.4 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:121726471 C>T maps to NM_005270.4 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr2:121746726 C>T maps to NM_005270.4 D1079D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr2:121747296 C>T maps to NM_005270.4 S1269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:121747230 T>C maps to NM_005270.4 Y1247Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr2:121708926 C>G maps to NM_005270.4 Y121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:121747563 G>A maps to NM_005270.4 P1358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr7:42088198 G>A maps to NM_000168.5 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr7:42007401 G>A maps to NM_000168.5 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr7:42005112 C>A maps to NM_000168.5 P1186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:42004863 G>A maps to NM_000168.5 D1269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr7:42005030 G>A maps to NM_000168.5 Q1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr7:42005907 G>A maps to NM_000168.5 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr7:42262803 C>A maps to NM_000168.5 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr7:42005346 G>A maps to NM_000168.5 Y1108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr8:144358502 C>T maps to NM_138465.3 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:144358715 T>C maps to NM_138465.3 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr8:144351565 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr8:144356907 G>A maps to NM_138465.3 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr8:144358775 C>T maps to NM_138465.3 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr12:75728516 G>A maps to ENST00000378695 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:54060428 C>A maps to NM_147193.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:54060248 C>T maps to NM_147193.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr16:4385104 C>G maps to NM_032575.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr9:3828334 G>A maps to NM_001042413.1 F910F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr9:4118289 T>C maps to NM_001042413.1 Q396Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr9:4286389 C>A maps to NM_001042413.1 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr9:4125840 G>A maps to NM_001042413.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:92752070 G>A maps to NM_053274.2 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:92752142 G>A maps to NM_053274.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:92757088 G>A maps to NM_053274.2 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:92712693 C>T maps to NM_053274.2 Q531Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr6:38649845 G>T maps to NM_006708.2 Y136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:38670779 G>A maps to NM_006708.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr6:38670779 G>T maps to NM_006708.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr6:38650626 C>T maps to NM_006708.2 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr23:48631762 G>A did not map to a codon.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr23:48631835 C>A did not map to a codon.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr23:48631818 C>A did not map to a codon.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr6:39047366 C>A maps to NM_002062.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr17:9757846 G>A maps to NM_004246.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:151231106 C>G maps to NM_001146040.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:14627312 G>T did not map to a codon.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr23:14625372 C>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:14708968 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr23:14550395 G>C did not map to a codon.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr23:14599364 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:14708974 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr23:14622469 G>A did not map to a codon.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr4:175565074 C>T maps to NM_006529.2 K419K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr4:175565131 T>A maps to NM_006529.2 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:102974113 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr23:102968472 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr23:102978789 C>G did not map to a codon.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr10:131959122 C>T maps to NM_006541.4 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:191818301 G>C maps to NM_014905.3 V554V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:56868839 G>C maps to NM_013267.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr12:56865967 G>C maps to NM_013267.2 S508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr19:17690355 C>T maps to NM_024656.2 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:17692012 C>G maps to NM_024656.2 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:183920229 G>C maps to NM_015101.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:183920241 G>A maps to NM_015101.2 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:183933110 C>A maps to NM_015101.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr9:138516425 G>A maps to NM_182974.2 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr3:52730303 G>A maps to NM_018446.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:104388222 G>A maps to NM_031302.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:104387227 C>T maps to NM_031302.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr12:110318077 G>A maps to NM_016433.3 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr12:110290443 G>C maps to NM_016433.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:110290443 G>C maps to NM_016433.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr12:110290359 C>G maps to NM_016433.3 *210Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:1262983 C>T maps to NM_001029885.1 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:1262842 G>A maps to NM_001029885.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:1263142 G>C maps to NM_001029885.1 *215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr19:48205452 C>T maps to NM_015711.3 S1488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:48205332 G>A maps to NM_015711.3 P1448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr19:48204666 C>T maps to NM_015711.3 P1226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:88818907 G>A maps to NM_005271.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr10:88854363 C>A maps to NM_005271.3 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr10:88854259 C>T maps to NM_005271.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr10:88818976 C>T maps to NM_005271.3 K444K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:120182007 G>C did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr23:120183006 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:120182953 G>T did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:120181907 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr23:120181753 C>A did not map to a codon.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr23:120182899 G>C did not map to a codon.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr23:120182999 G>T did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:120183009 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:120181659 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr23:120182731 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr23:120182835 G>C did not map to a codon.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr1:182357737 C>G maps to NM_002065.5 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:182354933 G>A maps to NM_002065.5 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:58491918 G>T maps to NM_201648.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr11:58604798 C>T maps to NM_145016.3 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr11:58605775 G>A maps to NM_145016.3 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr3:52326568 G>A maps to NM_145262.3 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr16:4882141 C>T maps to NM_032569.3 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:4862197 G>A maps to NM_032569.3 Q391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr16:4882219 C>T maps to NM_032569.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr16:4873839 C>T maps to NM_032569.3 W202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr5:150632782 G>A maps to NM_000405.4 Q2Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr5:150646927 G>A maps to NM_000405.4 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:1624760 G>A maps to NM_001500.2 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:29030719 C>T maps to NM_006582.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:29037086 G>A maps to NM_006582.2 K318K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr14:54950454 C>A maps to NM_004124.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr19:19744824 G>A maps to NM_016573.2 Y753Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr19:19745887 G>A maps to NM_016573.2 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr19:19745720 G>A maps to NM_016573.2 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr8:143928066 G>C maps to NM_002066.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr8:143922582 C>T maps to NM_002066.2 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:220367144 G>A maps to ENST00000373917 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr6:16290711 C>G maps to NM_006877.3 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:16254923 C>T maps to NM_006877.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr6:16247182 G>A maps to NM_006877.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr6:16254926 G>A maps to NM_006877.3 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr14:24702482 G>A maps to ENST00000348719 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr14:24707567 G>T maps to ENST00000348719 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr14:24706314 C>T maps to ENST00000348719 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:155633962 C>T maps to NM_003875.2 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:155649628 C>T maps to NM_003875.2 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr3:155655449 C>G maps to NM_003875.2 S684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:3118954 G>C maps to NM_002067.2 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr19:3110264 C>T maps to NM_002067.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:3110297 G>A maps to NM_002067.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:3121020 C>T maps to NM_002067.2 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr19:3121080 C>T maps to NM_002067.2 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr17:63049661 G>A maps to NM_006572.4 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr17:63049730 G>A maps to NM_006572.4 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr9:80262685 G>A maps to NM_004297.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:80043924 C>T maps to NM_004297.3 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:3136547 G>T maps to NM_002068.2 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr19:3151743 C>T maps to NM_002068.2 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr19:3155895 C>T maps to NM_002068.2 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr7:79846721 C>G maps to NM_002069.5 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr7:79833068 C>T maps to NM_002069.5 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr3:50293653 G>A maps to NM_002070.2 Q165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr1:110134818 C>T maps to NM_006496.2 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr18:11689813 G>A maps to NM_182978.2 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr18:11752906 C>T maps to NM_182978.2 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr16:56385393 C>G maps to NM_020988.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr16:56388943 C>G maps to NM_020988.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr16:56309878 G>A maps to NM_020988.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr16:56374810 G>T maps to NM_138736.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr9:80409444 G>A maps to NM_002072.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr20:57429243 G>A maps to NM_080425.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr20:57484237 G>A maps to NM_080425.2 V827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:57485817 C>T maps to NM_080425.2 R1016R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr20:57429129 G>C maps to NM_080425.2 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr20:57485050 T>C maps to NM_080425.2 D938D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr3:50231194 C>T maps to NM_000172.3 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:50231305 C>A maps to NM_000172.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr3:50232061 C>T maps to NM_000172.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:110146627 G>C maps to NM_005272.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:110146642 G>A maps to NM_005272.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr22:23465560 C>T maps to NM_002073.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr22:23438385 T>C maps to NM_002073.2 Y168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr22:23438064 C>T maps to NM_002073.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr22:23438529 C>T maps to NM_002073.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr22:19794229 C>T maps to NM_053004.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr22:19799810 G>A maps to NM_053004.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr7:100276079 C>T maps to NM_005273.3 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr5:180668593 C>G maps to NM_006098.4 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr5:180666171 C>T maps to NM_006098.4 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr12:6952186 G>A maps to NM_002075.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:179119063 T>C maps to NM_021629.3 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr3:179137285 G>C maps to NM_021629.3 S35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr3:179123065 T>C maps to NM_021629.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr9:36276901 G>A maps to NM_001128227.2 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr9:36246415 C>G maps to NM_001128227.2 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr9:36217390 G>A maps to NM_001128227.2 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B0-01A-11D-A31L-08 chr7:93551506 G>T maps to NM_004126.3 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr11:62476274 C>G maps to NM_012202.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:84971732 A>C maps to NM_005274.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr19:47137867 G>A maps to NM_033258.1 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:30514512 G>A maps to NM_005275.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:38041279 C>T maps to NM_013285.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:38040349 G>T maps to NM_013285.2 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:38040357 C>A maps to NM_013285.2 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr1:38034698 G>A maps to NM_013285.2 Q541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:38034889 G>T maps to NM_013285.2 S477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:52726938 G>C maps to NM_014366.4 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:52721523 G>T maps to NM_014366.4 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr23:54584907 C>T did not map to a codon.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr23:54584977 C>T did not map to a codon.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr23:54585049 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr23:54569457 A>G did not map to a codon.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr23:54578062 C>G did not map to a codon.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr23:54578148 A>G did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr23:54566598 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr23:54578730 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:54574790 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:54581047 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr23:54578725 G>A did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr6:42930879 C>T maps to NM_018960.4 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr6:42930027 A>G maps to NM_018960.4 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:231402030 G>A maps to NM_014236.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr5:141382665 G>T maps to NM_005471.4 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr5:141385838 G>A maps to NM_005471.4 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:44709781 C>T maps to NM_138335.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr4:44724164 G>A maps to NM_138335.1 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr14:53248519 G>A maps to NM_198066.3 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr12:102158443 G>A maps to NM_024312.4 Q751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:102147301 C>G maps to NM_024312.4 L1150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:102155036 G>A maps to NM_024312.4 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:102157982 G>C maps to NM_024312.4 L904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:1412125 G>A maps to NM_032520.4 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr16:1411765 C>G maps to NM_032520.4 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr8:25279184 C>G did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:3025173 C>T maps to NM_001501.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr4:68619663 G>A maps to NM_000406.2 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:68619555 G>T maps to NM_000406.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:65116857 G>T maps to ENST00000418919 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr12:65137013 C>T maps to ENST00000418919 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:127691528 C>T maps to NM_002077.3 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr9:127652730 C>G maps to NM_002077.3 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr9:127650666 C>G maps to NM_002077.3 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr9:127644137 C>T maps to NM_002077.3 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:131019546 C>T maps to NM_004486.4 V936V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr9:131028090 G>A maps to NM_004486.4 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr9:131036203 C>T maps to NM_004486.4 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr9:131020359 G>A maps to NM_004486.4 Q776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:100551505 G>A maps to ENST00000266746 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr12:100551834 C>T maps to ENST00000266746 E6E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr12:133359052 C>T maps to NM_005895.3 K1098K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:133374949 G>T maps to NM_005895.3 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:133384935 G>C maps to NM_005895.3 S240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B0-01A-11D-A31L-08 chr12:133378550 G>A maps to NM_005895.3 H534H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:133381317 G>A maps to NM_005895.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr12:133378499 C>T maps to NM_005895.3 Q551Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr12:133389925 G>C maps to NM_005895.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:37376608 G>A maps to NM_001172713.1 K2108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr3:37340795 G>A maps to NM_001172713.1 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr3:37365136 C>G maps to NM_001172713.1 S609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr3:37357082 A>T maps to NM_001172713.1 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr3:37336565 C>T maps to NM_001172713.1 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:37368569 G>A maps to NM_001172713.1 Q1753Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr3:37368268 C>G maps to NM_001172713.1 S1653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:37365275 C>G maps to NM_001172713.1 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr3:37367048 C>A maps to NM_001172713.1 T1246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMW-01A-11D-A42E-08 chr3:37396629 T>C maps to NM_001172713.1 P2220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:37367408 G>A maps to NM_001172713.1 L1366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:93264298 G>T maps to NM_005113.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr14:93299598 C>T maps to NM_005113.2 Q618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr14:93264128 C>G maps to NM_005113.2 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr14:93278100 T>G did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr15:72954782 C>T maps to NM_018652.4 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr15:72954611 G>A maps to NM_018652.4 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr15:75562494 G>T maps to NM_001164404.1 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:41355113 C>T maps to NM_001002296.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr10:99623772 C>T maps to NM_001010917.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr15:34673685 C>A maps to NM_181077.3 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr15:34673686 C>T maps to NM_181077.3 Q579Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:121413279 C>T maps to ENST00000393667 Q2030Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:121414424 G>A maps to ENST00000393667 Q1649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:121416257 C>A maps to ENST00000393667 E1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:121416387 C>T maps to ENST00000393667 E994E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr3:121413221 G>A maps to ENST00000393667 L2050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:121414328 C>A maps to ENST00000393667 E1681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:121414659 G>A maps to ENST00000393667 L1570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr3:121416399 C>T maps to ENST00000393667 K990K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr3:121441138 G>C maps to ENST00000393667 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr3:121416267 G>A maps to ENST00000393667 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:121414110 C>T maps to ENST00000393667 E1753E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:121409867 G>C maps to ENST00000393667 L2781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr3:121435851 G>A maps to ENST00000393667 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:121410944 C>T maps to ENST00000393667 L2422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr3:121395811 G>C maps to ENST00000393667 L3035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr3:121396152 G>C maps to ENST00000393667 L3006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr3:121448181 C>T maps to ENST00000393667 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr3:167750309 C>A maps to NM_014498.3 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:167759262 C>G did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr3:167812962 C>T maps to NM_014498.3 Q37Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr5:32126709 G>A maps to NM_022130.3 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:204170900 C>T maps to NM_198447.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr1:155734859 G>A maps to ENST00000368331 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr1:155742959 G>A maps to ENST00000368331 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:155823270 G>A maps to ENST00000368331 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:155721968 C>T maps to ENST00000368331 V2085V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:155744960 C>A maps to ENST00000368331 E728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:155791330 G>A maps to ENST00000368331 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr1:155774914 G>A maps to ENST00000368331 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr1:155727115 T>G did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:155735083 G>A maps to ENST00000368331 Q1394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:155735904 G>C maps to ENST00000368331 S1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:155783559 G>A maps to ENST00000368331 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:117884439 G>A maps to NM_020399.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr6:117923232 C>T maps to NM_020399.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:39139936 C>T maps to NM_031899.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr17:28808203 G>A maps to NM_004871.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr17:45012561 G>A maps to NM_001012511.1 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:45008504 C>T maps to NM_054022.2 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr16:58756065 C>T maps to NM_002080.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr16:20329745 C>G maps to NM_001007240.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:194118413 G>A maps to NM_004488.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:194118120 C>G maps to NM_004488.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:194117343 C>T maps to NM_004488.2 E556E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr3:194118297 G>A maps to NM_004488.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr3:194118923 G>T maps to NM_004488.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr3:194117862 G>A maps to NM_004488.2 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr3:194118711 C>T maps to NM_004488.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr19:55543594 C>T maps to NM_001083899.1 K79K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr19:55525587 C>G maps to NM_001083899.1 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:167059488 G>C maps to NM_005814.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:167024973 G>C maps to NM_005814.1 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:145140308 G>T maps to NM_003801.3 E460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr8:145139046 G>A maps to NM_003801.3 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr8:145139642 C>T maps to NM_003801.3 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:113928631 G>C maps to NM_020918.4 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:113928679 G>A maps to NM_020918.4 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr2:96690304 C>T maps to NM_207328.2 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:33579136 C>T maps to NM_018025.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:33600725 G>A maps to NM_018025.2 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:217784237 G>A maps to NM_018040.2 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr1:27223949 C>A maps to NM_022078.2 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:27220739 C>T maps to NM_022078.2 Q346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr1:156565922 A>G maps to NM_015590.3 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:42513872 G>C maps to NM_001002909.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr17:42475103 G>A maps to NM_001002909.2 I1447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr17:42478100 C>A maps to NM_001002909.2 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:42478049 C>T maps to NM_001002909.2 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr5:56558559 C>A maps to NM_001127236.2 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr1:46120319 G>A maps to NM_021639.4 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:46099286 G>A maps to NM_021639.4 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:241398600 C>T maps to NM_002081.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr2:241404540 C>T maps to NM_002081.2 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr7:99771456 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr7:99768079 C>A maps to NM_152742.1 G505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr23:132670203 A>C did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:132440161 C>G did not map to a codon.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr23:132437353 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr23:132548971 C>T did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:132445451 C>A did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr13:92560197 C>T maps to NM_004466.4 Q430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr13:92101126 C>T maps to NM_004466.4 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr13:92345939 C>G maps to NM_004466.4 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr13:92560308 C>T maps to NM_004466.4 Q467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr13:93518664 G>T maps to NM_004466.4 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr13:92797147 C>A maps to NM_004466.4 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr13:92560229 G>A maps to NM_004466.4 Q440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr13:94482414 C>T maps to NM_005708.3 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:95034696 C>T maps to NM_005708.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr13:95034741 C>T maps to NM_005708.3 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr13:95034780 C>T maps to NM_005708.3 C422C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr13:94482692 C>T maps to NM_005708.3 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr12:50501348 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr3:32181751 C>G maps to NM_015141.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr2:157406138 G>A maps to NM_000408.4 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr2:157406240 G>A maps to NM_000408.4 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:157435458 C>G maps to NM_000408.4 S609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr7:1131642 C>T maps to NM_001505.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr7:1131483 C>T maps to NM_001505.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr7:1132275 C>T maps to NM_001505.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr7:1131765 G>A maps to NM_001505.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr7:1132272 C>T maps to NM_001505.2 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr14:63779779 G>A maps to ENST00000314140 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr14:67291199 G>A maps to NM_020806.4 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr14:67555730 A>G maps to NM_020806.4 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr19:34884958 G>T maps to NM_000175.3 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:34884964 C>T maps to NM_000175.3 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:34868415 G>C maps to NM_000175.3 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:48973497 C>T did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:48976103 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr6:24433444 G>A maps to NM_001503.2 S802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47W-01A-11D-A23U-08 chr4:176556181 G>T maps to NM_005277.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:176561939 G>A maps to NM_005277.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:13791014 G>C did not map to a codon.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr23:13792690 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr23:13791095 G>T did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr2:27858050 G>A maps to NM_007266.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:27862953 C>G maps to NM_007266.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:27851918 G>A maps to NM_007266.3 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:27216179 G>A maps to NM_018066.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:27210661 G>A maps to NM_018066.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr1:27216281 G>T maps to NM_018066.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:27216179 G>A maps to NM_018066.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:27212529 G>C maps to NM_018066.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr7:23313758 C>G maps to ENST00000435486 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:23300225 C>T maps to ENST00000435486 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr7:23313137 A>G did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:23299746 C>T maps to ENST00000435486 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr2:207041650 G>A maps to NM_005279.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr23:136113100 C>G did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr23:136113143 C>G did not map to a codon.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr23:136113449 A>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr23:136112837 C>A did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr23:136113077 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr23:136113396 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr23:136113173 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr23:136113743 G>A did not map to a codon.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr23:136112887 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr23:136112977 C>A did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:136113686 G>A did not map to a codon.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr9:132890953 T>C maps to NM_001136557.1 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr9:132897342 C>G maps to NM_001136557.1 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr9:132889829 G>A maps to NM_001136557.1 W523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:132854561 C>G maps to NM_001136557.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr9:132890959 G>A maps to NM_001136557.1 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr19:6731900 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr19:6730395 C>A did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr19:6732094 C>T maps to NM_001080452.1 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr12:123187284 G>A maps to NM_177551.3 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr12:123187065 G>A maps to NM_177551.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr12:123186798 C>T maps to NM_177551.3 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr12:123187821 C>T maps to NM_177551.3 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr12:123200588 G>A maps to NM_006018.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr6:46977847 G>A maps to ENST00000283297 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:46977463 G>A maps to ENST00000283297 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:46996734 G>A maps to ENST00000283297 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr6:46977667 G>A maps to ENST00000283297 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr6:46979842 G>T maps to ENST00000283297 S340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:46977490 C>T maps to ENST00000283297 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr23:135494523 T>C did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr23:135429690 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr23:135428140 T>G did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr23:135431714 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:135482092 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr23:135498611 G>C did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr23:135431842 C>G did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:135431320 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr23:135428057 G>C did not map to a codon.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr23:135453498 A>G did not map to a codon.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr23:135427030 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:135430469 G>A did not map to a codon.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr23:135428932 C>G did not map to a codon.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr23:135443723 G>T did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr23:135441567 A>G did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:135427926 G>C did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:135405404 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:135427823 G>C did not map to a codon.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr23:135429264 G>A did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:135428785 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr23:135428582 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr23:135430770 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr23:135430299 A>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr23:135427061 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:135427389 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:135427504 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr23:135453570 T>G did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:135453602 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:26533880 G>T maps to NM_001145168.1 Y905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:26532907 C>G maps to NM_001145168.1 V1048V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:57608777 C>T maps to ENST00000349457 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr16:57600605 C>G maps to ENST00000349457 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr16:57608972 G>T maps to ENST00000349457 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr6:46825934 A>G maps to NM_015234.4 G1235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:46825919 G>A maps to NM_015234.4 F1240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr23:129518616 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:129518432 C>A did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:129519380 A>C did not map to a codon.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr23:129518814 C>T did not map to a codon.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr13:27333760 G>A maps to NM_005288.3 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr10:95335855 G>T maps to NM_181745.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:134940808 C>T maps to ENST00000368577 Y699Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr8:37690566 C>T maps to NM_032777.9 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr4:22449099 G>A maps to NM_145290.2 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:22456498 G>A maps to NM_145290.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr4:22390724 C>T maps to NM_145290.2 R903R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr4:22438264 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr6:142764615 C>T maps to NM_198569.2 I1239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr6:142764630 C>T maps to NM_198569.2 F1244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr3:100368556 C>T maps to NM_032787.2 Q429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr3:100364942 T>C maps to NM_032787.2 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr3:100354609 C>T maps to NM_032787.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:100354654 A>G maps to NM_032787.2 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr3:100364837 C>T maps to NM_032787.2 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:131498797 G>A maps to NM_198827.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr12:131488788 G>A maps to NM_198827.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr12:131487770 C>T maps to NM_198827.3 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:131471688 G>A maps to NM_198827.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr12:131476908 C>A maps to NM_198827.3 S313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr12:131476885 C>T maps to NM_198827.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr12:131487740 G>A maps to NM_198827.3 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr12:131593351 C>T maps to NM_198827.3 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr12:131620620 G>C maps to NM_198827.3 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr12:131569126 G>A maps to NM_198827.3 T530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:64054073 G>A maps to NM_001170726.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr11:64051852 G>A maps to NM_001170726.1 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr11:64056791 G>A maps to NM_001170726.1 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:64054106 C>T maps to NM_001170726.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:64055318 G>A maps to NM_001170726.1 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:236306308 C>G maps to NM_003272.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:20084881 G>T maps to NM_001002911.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr16:20043131 C>T maps to NM_001002911.2 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:72366741 C>T maps to ENST00000440684 I1110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr17:72368384 G>A maps to ENST00000440684 R1308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:9707572 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:154139249 G>A maps to NM_001038705.1 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr3:154138907 G>A maps to NM_001038705.1 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:154146531 C>T maps to NM_001038705.1 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr3:154146540 G>A maps to NM_001038705.1 C288C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr3:154147035 C>T maps to NM_001038705.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr3:98251956 C>G maps to NM_005290.1 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:145895382 C>T maps to NM_194251.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr11:67219577 G>C maps to NM_206997.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr2:175338036 C>T maps to NM_152529.5 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:175304648 G>A maps to NM_152529.5 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr2:175337919 G>T maps to NM_152529.5 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr1:9164615 G>C maps to NM_024980.4 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:9188804 G>A maps to NM_024980.4 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:25883234 C>G maps to NM_020752.2 S636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr10:25887392 A>C maps to NM_020752.2 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:25464702 G>A maps to NM_020752.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr10:25887391 C>G maps to NM_020752.2 S946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr10:25888024 C>G maps to NM_020752.2 S1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr10:25464573 C>T maps to NM_020752.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:168073911 G>A maps to NM_153832.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:168056840 C>A maps to NM_153832.1 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr1:168054930 G>A maps to NM_153832.1 I476I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:6933171 C>G maps to NM_019858.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr12:6935948 C>T maps to NM_019858.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr2:128408389 G>A maps to NM_005291.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr2:128409175 C>T maps to NM_005291.2 N317N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr2:128409307 G>A maps to NM_005291.2 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:128408719 C>G maps to NM_005291.2 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr3:150916248 G>A maps to NM_013308.3 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr3:150916871 G>C maps to NM_013308.3 S101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr3:150916711 G>A maps to NM_013308.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:145583547 C>T maps to NM_024531.3 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr8:145583670 G>A maps to NM_024531.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr8:145583959 C>T maps to NM_024531.3 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr8:145582985 G>A maps to NM_024531.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr23:53106390 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:53106307 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr23:53106213 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr23:53106252 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:53106819 C>G did not map to a codon.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr23:53106047 C>G did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:78427377 T>C did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr23:78427143 G>A did not map to a codon.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr23:78427385 T>A did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:78427092 C>G did not map to a codon.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr15:40212134 G>A maps to NM_007223.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr15:40093493 G>A maps to NM_007223.1 Q463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr17:36498938 C>T maps to ENST00000398597 W245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr17:36485623 C>T maps to ENST00000398597 S1277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr17:36486595 C>T maps to ENST00000398597 R953R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr17:36487081 C>T maps to ENST00000398597 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr17:36482905 G>A maps to ENST00000398597 V2183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:36486037 C>T maps to ENST00000398597 V1139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:36486037 C>T maps to ENST00000398597 V1139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:36486124 C>T maps to ENST00000398597 E1110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:36487273 G>A maps to ENST00000398597 F727F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr13:99908093 G>C maps to NM_005292.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr12:57390078 C>T maps to NM_007264.3 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr12:57389568 C>T maps to NM_007264.3 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr12:12815129 G>A maps to NM_006143.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:12814652 G>A maps to NM_006143.2 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr8:142367849 C>G maps to NM_005293.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr8:142367699 C>T maps to NM_005293.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:125797111 C>T maps to NM_005294.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr9:125797423 G>T maps to NM_005294.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr7:107115789 C>T maps to NM_005295.2 Q429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:107115257 G>A maps to NM_005295.2 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr10:125447474 C>T maps to NM_153442.3 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:71804309 G>C maps to NM_018971.1 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr1:27721051 C>T maps to NM_005281.2 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr6:167571250 C>T maps to NM_005299.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr6:167571196 G>A maps to NM_005299.2 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr6:167571223 G>A maps to NM_005299.2 N32N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr6:167570934 G>A maps to NM_005299.2 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr19:51274694 C>T maps to NM_001506.1 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:51274255 C>G maps to NM_001506.1 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:51274723 C>T maps to NM_001506.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr23:41555162 C>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:241569479 C>G maps to NM_001195381.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:241570079 G>C maps to NM_001195381.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:241570247 C>T maps to NM_001195381.1 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr7:124404703 G>T maps to NM_005302.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr7:124404067 G>A maps to NM_005302.2 H321H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:202097338 C>T maps to NM_004767.3 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:202096981 C>T maps to NM_004767.3 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr2:133174717 C>T maps to NM_001508.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr19:46094962 G>A maps to NM_005282.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:46094947 G>A maps to NM_005282.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr19:46095007 C>T maps to NM_005282.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr19:46094161 G>A maps to NM_005282.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:46094839 G>A maps to NM_005282.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:60620310 G>A maps to NM_004778.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:105859328 G>A maps to NM_007227.3 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr2:105859133 C>T maps to NM_007227.3 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr2:105858929 C>T maps to NM_007227.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr23:150349473 C>A did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr23:150349382 C>G did not map to a codon.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr23:150349250 C>T did not map to a codon.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr23:150349434 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr23:150345316 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr23:150349066 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:150349466 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:150349530 C>A did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr23:150348264 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr23:150349049 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr23:150349202 C>A did not map to a codon.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr23:150349687 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr23:150349124 C>T did not map to a codon.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr1:174417722 G>A maps to NM_005684.4 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:231775566 G>C maps to NM_005683.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:57685348 T>G maps to NM_005682.5 L101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:57695839 C>T maps to NM_005682.5 V638V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr16:57689409 C>T maps to NM_005682.5 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr16:57693504 C>G maps to NM_005682.5 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr16:57693540 C>G maps to NM_005682.5 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr16:57693570 C>G maps to NM_005682.5 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr16:57695845 C>G maps to NM_005682.5 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr16:57685529 C>T maps to NM_005682.5 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr16:57697427 G>T maps to NM_005682.5 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr16:57693480 C>A maps to NM_005682.5 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr16:57695752 G>T maps to NM_005682.5 V609V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:110301402 G>A maps to ENST00000414000 *378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:110086285 C>T maps to NM_031936.4 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:110086420 C>G maps to NM_031936.4 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:110086531 C>T maps to NM_031936.4 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:110086714 C>G maps to NM_031936.4 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:110086723 C>T maps to NM_031936.4 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr1:110085874 C>G maps to NM_031936.4 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr3:51990279 G>A maps to NM_080865.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr3:51990555 C>G maps to NM_080865.3 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:51990759 G>A maps to NM_080865.3 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr6:97246650 G>C maps to NM_030784.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr6:97246728 G>A maps to NM_030784.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:19032081 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr23:19014181 C>G did not map to a codon.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr23:19031966 G>A did not map to a codon.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr23:19013026 G>C did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:19049103 G>C did not map to a codon.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr23:19022952 C>T did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr23:19021017 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:19017390 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr23:19009040 G>T did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr23:19086861 G>A did not map to a codon.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr14:91700959 G>A maps to ENST00000238699 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr14:91700689 G>A maps to ENST00000238699 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr14:91700959 G>A maps to ENST00000238699 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr2:54080438 G>A maps to NM_006794.2 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr2:54080966 G>A maps to NM_006794.2 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr2:54080792 G>A maps to NM_006794.2 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:47844238 G>T maps to NM_018485.1 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr19:47844578 C>T maps to NM_018485.1 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:8583002 G>A maps to NM_080819.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:8588876 G>A maps to NM_080819.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr4:8588831 C>T maps to NM_080819.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:123214721 G>A maps to NM_032554.3 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:123214481 G>A maps to NM_032554.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:123214319 G>A maps to NM_032554.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:123214088 G>A maps to NM_032554.3 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr23:41586574 T>C did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:94134383 G>T maps to NM_016540.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:94113881 G>A maps to NM_016540.3 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:54756621 G>A maps to NM_020370.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr7:112724515 C>T maps to NM_018970.6 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:101004981 C>T maps to NM_022049.2 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr1:101005448 C>T maps to NM_022049.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:57710247 C>T maps to NM_170776.4 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr16:57719644 C>T maps to NM_170776.4 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr16:57710201 C>G maps to NM_170776.4 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:57719797 C>G maps to NM_170776.4 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr5:90041534 G>T maps to NM_032119.3 E3633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr5:89985849 A>T maps to NM_032119.3 A2221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:90449159 G>A maps to NM_032119.3 L6249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr5:90078971 A>G maps to NM_032119.3 P4421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:90149229 G>A maps to NM_032119.3 L5778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr5:90086838 G>A maps to NM_032119.3 V4731V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr5:89943313 G>C did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr5:90055401 G>A maps to NM_032119.3 K4039K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr5:89990018 C>A maps to NM_032119.3 Y2482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr5:89923174 G>T maps to NM_032119.3 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr5:89923140 C>A maps to NM_032119.3 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr5:90059210 C>A maps to NM_032119.3 V4070V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr5:90106457 T>C maps to NM_032119.3 N5127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr5:90079730 A>C maps to NM_032119.3 R4504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr5:90368420 G>T maps to NM_032119.3 E6104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr5:90281276 T>A maps to NM_032119.3 V6030V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr5:90261234 C>T maps to NM_032119.3 L5954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr5:90074320 G>C maps to NM_032119.3 L4248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr23:101910482 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr23:101912846 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr23:101912101 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr23:101911835 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr23:101912345 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr23:101911853 T>C did not map to a codon.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr23:101912427 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr23:101909066 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:101910964 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr23:101911663 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr23:101970820 C>T did not map to a codon.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr23:101972177 G>C did not map to a codon.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr23:101972242 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:101971348 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr23:101972057 A>C did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr23:101970045 T>G did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:101970155 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:101970854 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:13061779 C>T maps to NM_003979.3 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr17:72436223 C>T maps to NM_022036.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:72436907 G>A maps to NM_022036.2 Q376Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr17:72436479 C>T maps to NM_022036.2 Q234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr12:13102643 C>T maps to NM_018654.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr12:13103183 G>C maps to NM_018654.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:117128366 C>T maps to NM_148963.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:117114159 G>C maps to NM_148963.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr6:117130528 G>C maps to NM_148963.2 S149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr10:46999674 G>A maps to NM_014696.3 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr4:90170163 C>T maps to NM_198281.2 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr4:90170046 T>C maps to NM_198281.2 Q405Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr17:80010253 T>C maps to NM_212492.1 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr17:80012788 C>T maps to NM_212492.1 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr17:80012511 G>T maps to NM_212492.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr17:7216890 G>A maps to NM_004489.4 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr17:7217457 G>T maps to NM_004489.4 S113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr17:7216946 G>A maps to NM_004489.4 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:7217446 G>A maps to NM_004489.4 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:7217706 C>A maps to NM_004489.4 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:7217688 G>A maps to NM_004489.4 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr17:7217396 A>C did not map to a codon.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr9:139228939 C>T maps to NM_001145638.1 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:145729779 G>A maps to NM_005309.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr8:145731255 C>T maps to NM_005309.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr8:145732223 C>T maps to NM_005309.2 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:46962902 C>T maps to NM_133443.2 Y522Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr3:49394856 G>T maps to NM_000581.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr5:150406999 C>T maps to NM_002084.3 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:150404950 C>T maps to NM_002084.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr6:28497367 A>G maps to NM_001509.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr6:28500170 G>T maps to NM_001509.2 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:35512679 G>A maps to NM_020895.3 R555R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr19:35505211 C>T maps to NM_020895.3 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:35517043 G>A maps to NM_020895.3 *725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:35513812 G>T maps to NM_020895.3 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:35500043 G>C maps to NM_020895.3 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr11:123483471 C>G maps to ENST00000456860 V505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:123484241 T>G maps to ENST00000456860 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr3:113595067 C>G maps to NM_017577.4 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr15:72455647 C>T maps to NM_001012642.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr15:72454681 C>T maps to NM_001012642.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr15:72455647 C>T maps to NM_001012642.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr5:125824571 G>A maps to NM_023927.2 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr22:47071376 C>T maps to NM_015124.2 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr22:47073090 C>T maps to NM_015124.2 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr22:47062745 C>A maps to NM_015124.2 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr12:52408571 C>T maps to NM_181711.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr7:50673016 G>A maps to NM_005311.4 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr7:50660678 G>C maps to NM_005311.4 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr2:165378493 G>C maps to NM_004490.2 S271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr2:165365356 C>T maps to NM_004490.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:165353985 C>T maps to NM_004490.2 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:165349548 G>C maps to NM_004490.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr2:165350940 T>C maps to NM_004490.2 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:73316529 G>C maps to NM_002086.4 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr17:73316547 G>A maps to NM_002086.4 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr17:73322004 A>T maps to NM_002086.4 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr17:37901233 C>T maps to ENST00000445327 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr17:37898866 C>T maps to ENST00000445327 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:37901233 C>T maps to ENST00000445327 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr2:11735422 G>A maps to NM_014668.3 A581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:11765298 C>T maps to NM_014668.3 D1389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr2:11773123 G>A maps to NM_014668.3 V1642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:11706765 C>T maps to NM_014668.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr2:11716614 A>G maps to NM_014668.3 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr2:11750939 C>T maps to NM_014668.3 I931I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr2:11725903 C>T maps to NM_014668.3 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr2:11758777 C>T maps to NM_014668.3 V1259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:11720920 G>A maps to NM_014668.3 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:11735505 G>T did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:240656502 G>A maps to NM_022469.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:240656295 C>T maps to NM_022469.3 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr2:10104362 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:10126391 C>T maps to NM_198182.2 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:10101493 C>T maps to NM_198182.2 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:10105452 C>T maps to NM_198182.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:10095214 C>G maps to NM_198182.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr8:102570784 C>T maps to NM_024915.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr8:102555639 C>T maps to NM_024915.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr8:102589685 C>G maps to NM_024915.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr8:102589736 C>G maps to NM_024915.3 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:24668747 G>A maps to NM_021180.3 K402K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:24661178 G>A maps to NM_021180.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr1:24674003 C>G maps to NM_021180.3 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr9:37428495 G>T maps to ENST00000377824 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr5:153026644 C>T maps to NM_001114183.1 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr5:153144152 C>A maps to NM_001114183.1 Y661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr5:153056615 G>A maps to NM_001114183.1 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr5:152870471 C>T maps to NM_001114183.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr5:153054127 G>A maps to NM_001114183.1 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr4:158281082 C>T maps to NM_000826.3 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr4:158257875 G>A maps to NM_000826.3 Q607Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr4:158238832 T>G maps to NM_000826.3 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr4:158257602 C>T maps to NM_000826.3 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr4:158257893 G>T maps to NM_000826.3 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr4:158256914 C>T maps to NM_000826.3 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr23:122561867 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:122561888 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:122598815 G>A did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr23:122459963 T>C did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:122598871 G>C did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:122318436 T>C did not map to a codon.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr11:105481795 G>A maps to NM_000829.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr11:105732927 A>G maps to NM_000829.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr11:105795421 G>T maps to NM_000829.3 E592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr11:105481744 G>A maps to NM_000829.3 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr10:87373286 G>C maps to NM_017551.2 L826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr10:87484415 G>T maps to NM_017551.2 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr10:87487629 G>T maps to NM_017551.2 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr10:87379622 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr10:87628829 C>T maps to NM_017551.2 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr10:87898677 G>A maps to NM_017551.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:94344112 C>A maps to NM_001510.2 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr4:94690462 G>A maps to NM_001510.2 Q821Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr4:93511381 C>T maps to NM_001510.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:94690399 G>A maps to NM_001510.2 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr4:94343959 T>A maps to NM_001510.2 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr4:94344055 C>T maps to NM_001510.2 H494H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr4:94138008 C>T maps to NM_001510.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr4:94693315 C>A maps to NM_001510.2 T897T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr21:30959909 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr6:102134191 G>A maps to NM_021956.4 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:102307193 C>T maps to NM_021956.4 D450D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr6:102250291 G>C maps to NM_021956.4 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr6:102483433 T>C maps to NM_021956.4 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr6:102124636 C>A maps to NM_021956.4 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr6:102337648 C>T maps to NM_021956.4 F553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:37337827 G>A maps to NM_000831.3 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr1:37271927 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr1:37270761 C>T maps to NM_000831.3 E797E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:37319266 C>T maps to NM_000831.3 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:37356631 G>A maps to NM_000831.3 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr1:37271788 C>A maps to NM_000831.3 E744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr1:37319236 C>A maps to NM_000831.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:37315962 A>G maps to NM_000831.3 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:37337944 G>A maps to NM_000831.3 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr11:120856884 G>A maps to NM_014619.2 Q929Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr11:120531032 C>T maps to NM_014619.2 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:120690612 C>T maps to NM_014619.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr11:120732771 G>A maps to NM_014619.2 Q283Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr19:42560969 G>A maps to NM_002088.3 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:42558024 G>A maps to NM_002088.3 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:42509941 G>A maps to NM_002088.3 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr19:42507537 G>A maps to NM_002088.3 F820F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:42526473 G>A maps to NM_002088.3 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:42563641 G>A maps to NM_002088.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr9:140051321 C>T maps to ENST00000371546 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr16:10274187 C>T maps to NM_000833.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr16:9984936 C>T maps to NM_000833.3 W343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr16:9923341 G>A maps to NM_000833.3 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr16:9858208 C>A maps to NM_000833.3 T1064T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr16:9923341 G>A maps to NM_000833.3 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr16:9862755 G>A maps to NM_000833.3 F849F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:13716781 C>T maps to NM_000834.3 R1130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr12:13716715 G>A maps to NM_000834.3 T1152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:13716010 G>A maps to NM_000834.3 F1387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr12:13768146 G>A maps to NM_000834.3 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:72846000 G>A maps to NM_000835.3 D521D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:72848654 G>A maps to NM_000835.3 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:72846449 G>C maps to NM_000835.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:72846042 G>A maps to NM_000835.3 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr17:72847787 G>A maps to NM_000835.3 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:48917337 C>T maps to NM_000836.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:48919323 C>T maps to NM_000836.2 I549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr19:48919344 C>T maps to NM_000836.2 F556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr19:48946602 G>A maps to NM_000836.2 P1140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:48908028 C>T maps to NM_000836.2 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr19:48917310 G>A maps to NM_000836.2 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr19:48908041 C>T maps to NM_000836.2 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:48908250 G>A maps to NM_000836.2 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr9:104448969 G>A maps to NM_133445.2 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr9:104449059 G>A maps to NM_133445.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:104432515 G>C maps to NM_133445.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr9:104432464 C>T maps to NM_133445.2 R743R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr12:66770814 C>T maps to ENST00000359742 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr12:66786235 C>T maps to ENST00000359742 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr12:66788017 G>C maps to ENST00000359742 S700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr12:67072645 C>T maps to ENST00000359742 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:66839202 G>A maps to ENST00000359742 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr3:14563281 C>T maps to ENST00000507975 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr3:14552781 G>T maps to ENST00000507975 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:48846410 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:48837883 C>T did not map to a codon.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr23:48834739 C>T did not map to a codon.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr23:48832430 G>T did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:48855859 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr23:48831590 G>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr10:121189892 G>A maps to NM_005308.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr10:121156214 T>A maps to NM_005308.2 Y90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr10:121207670 C>T maps to NM_005308.2 Q435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr10:121182721 G>A maps to NM_005308.2 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr10:121207651 G>A maps to NM_005308.2 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:176860604 C>T maps to NM_002082.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr5:176861045 C>T maps to NM_002082.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr5:176863485 C>T maps to NM_002082.3 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr5:176857940 C>T maps to NM_002082.3 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr5:176860649 C>T maps to NM_002082.3 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:141526644 G>A maps to NM_139209.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:141535744 C>T maps to NM_139209.2 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:141497287 G>A maps to NM_139209.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:47425166 C>T maps to NM_004491.4 Q1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:47440613 A>T maps to NM_004491.4 K1259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr19:47423516 C>T maps to NM_004491.4 R529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr19:47423287 G>A maps to NM_004491.4 W452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr19:47440646 G>T maps to NM_004491.4 E1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr19:47424855 C>G maps to NM_004491.4 S975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr19:47423812 G>A maps to NM_004491.4 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr19:47422105 C>T maps to NM_004491.4 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:47492837 G>A maps to NM_004491.4 V1314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr6:146720832 C>T maps to NM_000838.3 A886A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr6:146720820 G>A maps to NM_000838.3 G882G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr6:146720311 C>T maps to NM_000838.3 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:146350755 C>T maps to NM_000838.3 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr6:146351186 C>T maps to NM_000838.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr3:51747076 G>T maps to NM_000839.3 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr3:51743013 T>C maps to NM_000839.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr3:51747291 C>G maps to NM_000839.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:51749537 C>G maps to NM_000839.3 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr7:86468799 C>G maps to NM_000840.2 S657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:86416106 C>T maps to NM_000840.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr7:86479786 G>A maps to NM_000840.2 Q831Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr7:86394791 G>T maps to NM_000840.2 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:86468863 G>A maps to NM_000840.2 Q678Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr7:86415908 C>T maps to NM_000840.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:86479855 T>A maps to NM_000840.2 S854S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:34101144 G>A maps to NM_000841.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:33996116 C>A maps to NM_000841.1 T823T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:34101213 G>A maps to NM_000841.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr6:34100916 C>T maps to NM_000841.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:34059675 C>T maps to NM_000841.1 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr6:34003489 C>A maps to NM_000841.1 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr11:88780571 G>A maps to NM_001143831.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:88337911 G>A maps to NM_001143831.2 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr11:88583192 G>A maps to NM_001143831.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:88583123 C>T maps to NM_001143831.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr11:88780522 G>C maps to NM_001143831.2 S173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:88780575 G>T maps to NM_001143831.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr11:88780503 C>G maps to NM_001143831.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr11:88300390 C>T maps to NM_001143831.2 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr5:178413883 G>A maps to NM_000843.3 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr5:178408759 G>C maps to NM_000843.3 L844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:178413610 G>A maps to NM_000843.3 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr5:178413181 G>A maps to NM_000843.3 F691F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr3:6903440 C>T maps to NM_181874.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr3:6903419 G>A maps to NM_181874.2 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr3:7503405 C>G maps to NM_181874.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr3:7456817 C>G maps to NM_181874.2 S381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr3:7721872 C>T maps to NM_181874.2 F863F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr3:6903548 G>A maps to NM_181874.2 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:6903452 C>T maps to NM_181874.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:7782089 C>T maps to NM_000844.3 I915I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr3:7503306 G>C maps to NM_181874.2 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:7456753 A>C maps to NM_181874.2 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr7:126544098 T>A maps to NM_001127323.1 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr7:126086315 C>T maps to NM_001127323.1 Q847Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr7:126746601 C>T maps to NM_001127323.1 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:126882831 T>A maps to NM_001127323.1 K143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:42427116 C>G maps to NM_002087.2 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr18:56892848 G>T maps to NM_002091.3 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr4:7069741 C>A maps to NM_025196.2 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:16170437 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:16168426 G>C did not map to a codon.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr23:16142333 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr13:114009746 G>T maps to NM_024719.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr19:48956280 G>C maps to NM_031485.3 *447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr19:48953613 G>A maps to NM_031485.3 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr19:48956191 G>A maps to NM_031485.3 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr4:42895664 C>T maps to NM_001080476.2 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr4:42895367 C>T maps to NM_001080476.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:43032530 C>T maps to NM_001080476.2 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr4:42895342 C>T maps to NM_001080476.2 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr4:42965027 A>G maps to NM_001080476.2 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:145239352 C>T maps to NM_001080516.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:145252342 A>G maps to NM_001080516.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:145252371 G>A maps to NM_001080516.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr5:145252240 T>G maps to NM_001080516.1 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:95234905 C>T maps to NM_173849.2 W232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr22:19137310 C>A maps to NM_005315.1 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr22:19136548 C>T maps to NM_005315.1 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr22:19136518 C>T maps to NM_005315.1 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr17:38133154 C>T maps to NM_178171.4 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:38066074 C>A maps to NM_001165958.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:38068639 G>A maps to NM_001165958.1 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr8:130761711 G>A maps to NM_031415.2 Q425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr8:130760774 G>T maps to NM_031415.2 S500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr8:130760917 G>C maps to NM_031415.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:13240940 G>A maps to NM_001080555.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:13240195 A>T maps to NM_001080555.1 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:42744258 G>A maps to NM_019884.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:42736657 G>A maps to NM_019884.2 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:119720940 T>C maps to NM_002093.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr3:119582337 C>A maps to NM_002093.3 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr3:119562102 T>A maps to NM_002093.3 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:124065294 C>T maps to NM_000177.4 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr23:51488484 C>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:51488446 C>T did not map to a codon.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr23:51488288 G>C did not map to a codon.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr23:51486809 G>T did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:51488274 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr23:51488597 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:51486865 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr23:51486902 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:30560622 C>T maps to NM_000637.3 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:33533874 G>A maps to NM_000178.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr20:33519777 G>C maps to NM_000178.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr20:33519741 C>T maps to NM_000178.2 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr20:33533814 G>A maps to NM_000178.2 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr6:52698950 A>C maps to NM_153699.1 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:52701149 G>A maps to NM_153699.1 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr6:52701149 G>A maps to NM_153699.1 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr6:52696762 C>T maps to NM_153699.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr4:106640291 C>T maps to NM_001031720.2 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr4:106744226 G>A did not map to a codon.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr7:142962364 C>T maps to NM_001143679.1 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:142962177 G>A maps to NM_001143679.1 W126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:110230831 C>G maps to ENST00000369823 S26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:110211094 G>T maps to ENST00000369830 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:110211102 G>A maps to ENST00000369830 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:110211952 C>T maps to ENST00000369830 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr1:110211574 G>A maps to ENST00000369830 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:110280350 A>T maps to NM_000849.4 L132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr1:110280309 G>A maps to NM_000849.4 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:110280345 C>A maps to NM_000849.4 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:110199864 G>A maps to NM_000850.4 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:110255780 C>T maps to ENST00000369812 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr1:110257750 G>T did not map to a codon.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:110255279 C>G maps to ENST00000369812 S26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr10:106059003 C>T maps to NM_183239.1 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr10:106037864 A>G maps to NM_183239.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:67353984 C>G maps to NM_000852.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:67353994 C>T maps to NM_000852.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr22:24384186 G>A maps to NM_000853.2 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr22:24376502 G>A maps to NM_000853.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr22:24323193 G>T maps to NM_000854.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr4:54967809 G>T maps to NM_133267.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr4:54967815 C>G maps to NM_133267.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr4:54968054 C>G maps to NM_133267.2 S294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr4:54968001 G>C maps to NM_133267.2 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:144899574 G>C maps to NM_001164629.2 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr14:81659125 G>A maps to NM_015859.2 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:48848386 C>T maps to NM_172311.2 Q773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr2:48906487 G>A maps to NM_172311.2 K1152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:59942968 G>A maps to NM_004492.2 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr1:89323154 G>T maps to NM_001514.5 S184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr1:89323051 G>A maps to NM_001514.5 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr3:120469779 C>T maps to NM_005513.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:30472222 G>A maps to NM_002095.4 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr8:30511097 C>T maps to NM_002095.4 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:6389528 G>A maps to NM_002096.2 Y84Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr19:6392881 G>A maps to NM_002096.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr19:6389522 G>A maps to NM_002096.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr19:6380393 C>T maps to NM_002096.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr11:18373960 G>T maps to NM_005316.3 E410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr12:124144457 C>A maps to NM_001516.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr12:124144443 G>T maps to NM_001516.3 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr12:124123887 C>T maps to NM_001516.3 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:30881723 C>T maps to NM_001517.4 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr6:30879009 C>G maps to NM_001517.4 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr6:30880885 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr7:74114640 G>T maps to NM_032999.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr7:74160220 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:74166460 C>G maps to NM_032999.2 S839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr7:74004240 C>G maps to NM_016328.2 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:73971993 G>A maps to NM_016328.2 R698R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr7:73971981 G>A maps to NM_016328.2 A694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr7:73929846 C>T maps to NM_016328.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr7:74564076 C>T maps to NM_001003795.2 I608I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr13:28009277 C>T maps to NM_002097.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr13:28009277 C>T maps to NM_002097.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr16:27549622 C>T maps to NM_001520.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:27544707 C>T maps to NM_001520.3 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr16:27503821 C>T maps to NM_001520.3 L996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:27556789 C>G maps to NM_001520.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr16:27544610 C>A did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr16:27503785 G>A maps to NM_001520.3 C1008C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:27539997 C>G maps to NM_001520.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr16:27509994 G>A maps to NM_001520.3 I707I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr16:27512586 C>T maps to NM_001520.3 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr16:27518476 C>A maps to NM_001520.3 G415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr16:27518477 C>A did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr2:27551029 C>T maps to NM_001521.2 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:27552303 G>A maps to NM_001521.2 Q607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr2:197654056 C>T maps to NM_012086.2 W255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr2:197650252 G>C maps to NM_012086.2 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:197643677 G>A maps to NM_012086.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:197654764 G>A maps to NM_012086.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:197636625 G>C maps to NM_012086.2 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr2:197664308 G>T maps to NM_012086.2 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr2:197662606 G>C maps to NM_012086.2 S43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr2:197664326 C>T maps to NM_012086.2 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr9:135553560 G>C maps to NM_012204.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:135554238 G>C maps to NM_012204.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr9:135554355 G>A maps to NM_012204.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr9:135919181 C>T maps to NM_001122823.1 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr9:135906451 G>C maps to NM_001122823.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr22:39122300 C>T maps to NM_004286.4 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr22:39104860 G>A maps to NM_004286.4 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr22:39120311 G>A maps to NM_004286.4 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr7:90014311 G>A maps to NM_033107.3 K336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:89983833 C>A maps to NM_033107.3 S97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr6:43589889 C>T maps to NM_019096.3 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr6:43594084 C>T maps to NM_019096.3 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr6:43592643 G>A maps to NM_019096.3 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr6:43592646 G>A maps to NM_019096.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr19:17449794 C>T maps to NM_133644.3 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr10:1042069 G>C maps to NM_012341.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr10:1042090 C>A maps to NM_012341.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr10:1046669 C>T maps to NM_012341.2 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr10:1060189 C>T maps to NM_012341.2 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:60768598 C>T maps to NM_015666.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr20:60775940 C>T maps to NM_015666.3 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr3:112709977 G>A maps to NM_014170.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr3:112710055 C>T maps to NM_014170.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr22:46704597 C>T maps to NM_016426.6 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr22:46722392 G>A maps to NM_016426.6 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:46693368 G>A maps to NM_016426.6 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:46725394 G>C maps to NM_016426.6 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr22:46725346 C>T maps to NM_016426.6 C673C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr22:46725319 C>T maps to NM_016426.6 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr12:54857081 C>T did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr20:42355268 G>A maps to NM_176791.3 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr6:42146055 C>A maps to NM_000409.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr6:42146619 C>T maps to NM_000409.3 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:42147032 C>G maps to NM_000409.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr6:42146607 C>T maps to NM_000409.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr3:108626979 G>A maps to NM_005459.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:108626913 G>T maps to NM_005459.3 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr3:108635058 C>T maps to NM_005459.3 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr1:42621248 G>A maps to NM_007102.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr11:106810788 G>A maps to ENST00000282249 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:106849345 G>A maps to ENST00000282249 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr4:156634389 G>A maps to NM_001130684.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr4:156618261 G>T maps to NM_001130684.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr4:156638379 C>T maps to NM_001130684.1 Q548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr4:156632144 G>A maps to NM_001130684.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr4:156634300 T>C maps to NM_001130684.1 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr4:156643192 C>T maps to NM_001130684.1 R574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr12:14794014 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr12:14839132 G>C maps to NM_004963.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr12:14804397 C>A maps to NM_004963.3 V551V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr17:7906988 G>A maps to NM_000180.3 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr23:108652305 C>T did not map to a codon.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr23:108708375 C>A did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:108708418 T>G did not map to a codon.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr23:108628508 G>A did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr23:108718742 G>C did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:108718537 G>A did not map to a codon.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr23:108641907 A>G did not map to a codon.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr23:108619344 T>C did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:108636232 G>A did not map to a codon.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr23:108641916 C>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:108628457 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:108684644 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr4:44680683 C>T maps to NM_021927.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:228336364 G>A did not map to a codon.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr7:65444451 G>A maps to NM_000181.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr7:65444736 G>A maps to NM_000181.3 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr7:65429328 G>C maps to NM_000181.3 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr12:42491760 G>A maps to NM_173601.1 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr3:148714217 G>A maps to NM_004130.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr3:148714611 C>A maps to NM_004130.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr3:148744568 C>A maps to NM_004130.3 S301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:2799127 C>T did not map to a codon.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr23:2779645 G>A did not map to a codon.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr23:2793877 C>G did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:2795274 A>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:145041741 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr4:145035856 C>A maps to NM_002099.6 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:144922436 C>A did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:127453716 G>A maps to NM_002101.3 *129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr2:127447888 T>A did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:49481246 G>C maps to NM_002103.4 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr12:21716177 G>A maps to NM_021957.3 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr12:21711247 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr12:21716256 C>T maps to NM_021957.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr12:21711190 G>A maps to NM_021957.3 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr20:23351020 G>C maps to NM_022482.3 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr20:23350749 G>A maps to NM_022482.3 W603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr20:23345817 G>T maps to NM_022482.3 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr14:25101099 G>A maps to ENST00000382542 C222C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr14:25101255 C>T maps to ENST00000382542 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr5:54326340 G>T maps to NM_002104.2 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:548595 C>G maps to NM_005317.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:48723370 G>A maps to NM_181788.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr12:48723424 C>T maps to NM_181788.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:129034688 C>T maps to NM_006026.3 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr12:14927571 G>A maps to NM_177925.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr7:44874099 C>G maps to ENST00000421098 *182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr7:44880563 G>A maps to ENST00000421098 S96S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-A1AD-01A-11D-A13W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr10:71835425 G>A maps to NM_018649.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr10:71871381 C>T maps to NM_018649.2 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr23:103267743 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:73775019 C>T maps to NM_005324.3 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:73775040 G>A maps to NM_005324.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:73774794 C>A maps to NM_005324.3 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr12:31944992 C>T maps to NM_001013699.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr12:31944917 G>C maps to NM_001013699.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:9324096 C>T maps to NM_004285.3 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:9324431 C>G maps to NM_004285.3 S627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:9324567 C>A maps to NM_004285.3 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:9305293 C>T maps to NM_004285.3 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:42996987 G>C maps to NM_012205.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr2:43010466 G>A maps to NM_012205.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr10:115344030 T>C maps to NM_004132.3 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr6:105225169 C>T maps to NM_020771.3 W530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr6:105298850 G>C maps to NM_020771.3 S51*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-E5-A4TZ-01A-11D-A31L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr3:15633126 T>A maps to NM_012260.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:15613210 C>T maps to NM_012260.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:15624390 G>A maps to NM_012260.2 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr4:108955473 C>T maps to ENST00000351726 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr2:26414193 G>A maps to NM_000182.4 A739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:26416529 C>A maps to NM_000182.4 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:26427022 G>A maps to NM_000182.4 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr2:26486263 G>A maps to NM_000183.2 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr16:777535 C>G maps to NM_207112.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr12:96389490 G>A maps to NM_002108.2 N66N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr12:96370218 G>A maps to NM_002108.2 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr12:96368045 C>T maps to NM_002108.2 K646K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:96382018 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:96371824 C>A maps to NM_002108.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:96374448 C>T maps to NM_002108.2 E468E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr1:119927525 G>A maps to ENST00000361035 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:119929318 G>A maps to ENST00000361035 Q225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr17:39889021 G>A maps to ENST00000310778 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr17:39883362 C>A maps to ENST00000310778 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr17:39883354 G>A maps to ENST00000310778 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr17:39888325 G>A maps to ENST00000310778 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:156594200 G>A maps to NM_021817.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:156594396 G>A maps to NM_021817.2 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr1:156594413 G>A maps to NM_021817.2 W193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr19:19371874 G>A maps to NM_023002.2 H77H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr5:140070804 C>A maps to NM_002109.3 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:140076762 C>T maps to NM_012208.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr19:52222878 C>T maps to NM_001523.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr8:122626945 C>T maps to NM_005328.2 W354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr8:122626714 G>A maps to NM_005328.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr8:122641337 C>T maps to NM_005328.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:69143702 C>T maps to NM_005329.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:69143909 C>G maps to NM_005329.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:69148448 C>T maps to NM_005329.2 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:172803291 C>G maps to NM_003642.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr4:2241810 G>C maps to NM_024511.5 S288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr14:23424354 G>A maps to NM_017815.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr19:36108217 G>T maps to NM_015302.1 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr19:36110354 C>T maps to NM_015302.1 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr19:36110925 G>T maps to NM_015302.1 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr19:36113575 G>A maps to NM_015302.1 E575E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr19:36113893 G>A maps to NM_015302.1 *634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr19:36108211 C>T maps to NM_015302.1 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:19058380 G>C maps to NM_017645.3 S795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr9:19078278 G>C maps to NM_017645.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr23:152734664 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:152719917 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr19:17166704 G>A maps to NM_033417.1 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:17170415 G>T maps to NM_033417.1 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr16:227391 G>A maps to NM_000558.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr11:5255573 G>T maps to NM_000519.3 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr5:139725658 T>A maps to NM_001945.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:5269668 C>A maps to ENST00000440157 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:230775 C>A maps to NM_005331.4 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr16:231037 C>T maps to NM_005331.4 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr6:135318538 G>T maps to NM_006620.3 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr6:135308784 G>A maps to NM_006620.3 Q410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr6:135315009 T>G maps to NM_006620.3 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr6:135299849 A>G maps to NM_006620.3 F588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr16:202995 C>T maps to NM_005332.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:11130275 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr23:11135428 G>T did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:11133073 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr23:153225573 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:153223252 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr23:153229677 G>C did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr23:153236182 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr23:153224925 G>A did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:153224214 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr23:153225379 C>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr16:3073521 G>A maps to NM_017885.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr12:104487162 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr20:30676389 G>A maps to NM_002110.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr20:30672192 G>C did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr20:30672278 G>A maps to NM_002110.3 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr20:30674543 C>T maps to NM_002110.3 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr3:121350794 G>A maps to NM_005335.4 D453D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:121353154 G>A maps to NM_005335.4 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr3:121366282 C>T maps to NM_005335.4 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr5:45353207 C>A maps to NM_021072.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr5:45303808 G>A maps to NM_021072.2 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr5:45353207 C>G maps to NM_021072.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr5:45303772 G>A maps to NM_021072.2 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:45462007 G>A maps to NM_021072.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr5:45303767 G>A maps to NM_021072.2 H517H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr5:45262846 G>A maps to NM_021072.2 Q617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr5:45262532 G>A maps to NM_021072.2 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr5:45396773 G>A maps to NM_021072.2 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr5:45695922 G>A maps to NM_021072.2 Y91Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr19:613318 C>T maps to NM_001194.3 F552F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:615984 C>T maps to NM_001194.3 I727I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr1:155255678 C>T maps to NM_020897.1 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:155252453 C>T maps to NM_020897.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:155247575 C>T maps to NM_020897.1 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr1:155254984 C>T maps to NM_020897.1 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr15:73624588 G>T maps to NM_005477.2 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:73624576 G>A maps to NM_005477.2 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr15:73616165 C>A maps to NM_005477.2 A756A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr15:73615331 G>A maps to NM_005477.2 P1034P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:40336366 G>C maps to NM_001524.1 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr1:32092553 C>T maps to NM_001525.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr1:32089200 G>A maps to NM_001525.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:55119998 C>T maps to NM_001526.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr6:55039429 G>A maps to NM_001526.3 W15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:55142252 C>T maps to NM_001526.3 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr6:55147169 C>G maps to NM_001526.3 S418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr6:55147194 C>G maps to NM_001526.3 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:36393521 C>T maps to NM_014266.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr1:32797277 C>T maps to NM_004964.2 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr1:32768300 C>G maps to NM_004964.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:32796438 C>T maps to NM_004964.2 Y303Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr22:50686514 G>A maps to NM_032019.5 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr22:50688574 G>A maps to NM_032019.5 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr22:50688080 G>C maps to NM_032019.5 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:114265513 A>G maps to ENST00000398283 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr5:141008782 C>T maps to NM_003883.3 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr5:141014415 G>A maps to NM_003883.3 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr5:141008189 G>T maps to NM_003883.3 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:240061421 C>T maps to NM_006037.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr2:240078423 G>A maps to NM_006037.3 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr2:240061421 C>T maps to NM_006037.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr17:42165951 G>A maps to NM_001015053.1 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr17:42156556 G>A maps to NM_001015053.1 I1012I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr17:42168788 C>T maps to NM_001015053.1 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr23:48681848 G>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr23:48666513 G>T did not map to a codon.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr23:48673144 G>C did not map to a codon.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr23:48674018 G>C did not map to a codon.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr23:48674934 G>C did not map to a codon.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr23:48676745 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr23:48682371 A>G did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr23:48666704 A>G did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr23:48682409 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:48674403 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:48678569 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:48681428 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr23:48673271 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr12:48179545 G>A maps to NM_015401.3 L899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr12:48190869 C>T maps to NM_015401.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:48191919 G>C maps to NM_015401.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr23:71792544 C>T did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:71571611 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:71715032 C>T did not map to a codon.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr7:18633642 C>A maps to NM_178425.2 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr7:18767219 G>A maps to NM_178425.2 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr7:18975510 C>G maps to NM_178425.2 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:18705861 G>A maps to NM_178425.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:18625072 G>A maps to NM_178425.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:18625025 G>T maps to NM_178425.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr7:18687581 T>C maps to NM_178425.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr15:50534609 G>A maps to NM_002112.3 V612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr15:50535050 A>G maps to NM_002112.3 N465N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr15:91475080 C>A maps to ENST00000394272 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:156714023 G>A maps to NM_001126050.1 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr19:4499522 G>A maps to ENST00000301284 E537E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr19:4501208 C>G maps to ENST00000301284 S604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr15:83876121 G>C maps to NM_016073.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr15:83876118 G>A maps to NM_016073.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr23:6995397 T>C did not map to a codon.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr9:116136445 G>A maps to NM_031219.2 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr2:242169581 G>A maps to NM_005336.3 L1193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr2:242202200 G>A maps to NM_005336.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr2:242194814 G>A maps to NM_005336.3 Q352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr2:242169087 G>A maps to NM_005336.3 S1245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:83723963 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:83724351 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr23:83724048 G>A did not map to a codon.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr23:83724554 A>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:83723934 A>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:236744561 C>T maps to NM_018072.5 K905K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr1:236761246 C>T maps to NM_018072.5 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr1:236767272 C>T maps to NM_018072.5 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:236737980 G>A maps to NM_018072.5 Q1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:236714216 G>C maps to NM_018072.5 L2140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr1:236740249 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr1:236767260 G>A maps to NM_018072.5 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr16:50138885 C>T maps to NM_182922.2 Q653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr16:50118103 G>T maps to NM_182922.2 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr16:50118177 C>T maps to NM_182922.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr14:73989307 C>G maps to ENST00000334988 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr14:73980888 G>C maps to ENST00000334988 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr14:73964941 G>T maps to ENST00000334988 I774I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr14:73974897 C>T maps to ENST00000334988 K560K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr14:31828243 G>A maps to ENST00000389961 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:37283641 G>C maps to NM_019024.1 V780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr2:37234199 C>G maps to NM_019024.1 L1590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr2:37286068 C>T maps to NM_019024.1 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr17:58145063 T>C maps to NM_022070.4 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:58128215 G>A maps to NM_022070.4 F804F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr17:58134519 G>T maps to NM_022070.4 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr17:58147082 G>T maps to NM_022070.4 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr17:58121445 C>A maps to NM_022070.4 V1008V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr8:145254054 C>T maps to NM_032450.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr5:41004989 C>G maps to ENST00000296803 G1300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr5:41012714 C>T maps to ENST00000296803 L1036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:41009498 C>T maps to ENST00000296803 K1102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr5:41005641 G>A maps to ENST00000296803 F1286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr5:41057462 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr5:41065474 C>A maps to ENST00000296803 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr5:41054877 G>A maps to ENST00000296803 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:31574847 G>C maps to NM_015382.2 S2418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr14:31614066 G>C maps to NM_015382.2 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:31598385 G>A maps to NM_015382.2 I1397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr14:31675046 G>A maps to NM_015382.2 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr14:31570423 G>A maps to NM_015382.2 L2553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr14:31585596 C>T maps to NM_015382.2 L1821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr14:31642623 C>T maps to NM_015382.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr10:93220320 C>T maps to ENST00000446394 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr1:45475256 C>T maps to NM_024602.5 K286K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:45472632 G>T maps to NM_024602.5 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr1:45475298 G>A maps to NM_024602.5 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:45476219 G>A maps to NM_024602.5 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr7:43508601 C>G maps to NM_015052.3 R999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr7:43484651 G>A maps to NM_015052.3 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr7:43484921 G>A maps to NM_015052.3 T717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr7:43436488 G>C did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr7:43484792 C>T maps to NM_015052.3 D674D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:43484543 C>G maps to NM_015052.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr7:43484402 G>A maps to NM_015052.3 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:197080608 C>A maps to NM_020760.1 G1529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr2:197090584 G>A maps to NM_020760.1 F1309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:197106878 G>A maps to NM_020760.1 F1193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr2:197118737 C>T maps to NM_020760.1 E1145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr2:197183744 C>T maps to NM_020760.1 E623E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr2:197135930 C>T maps to NM_020760.1 R1107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr2:197080653 G>T maps to NM_020760.1 L1514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:124738227 G>C maps to NM_020733.1 S489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr3:124720696 T>C maps to NM_020733.1 R1172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr3:124692598 G>A maps to NM_020733.1 L1324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:124739839 G>A maps to NM_020733.1 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:124732147 G>A maps to NM_020733.1 Q759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:66698777 C>G maps to NM_033647.2 S152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr12:66696553 C>T maps to NM_033647.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr12:66712453 A>G maps to NM_033647.2 E679E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr10:96306212 T>C maps to NM_018063.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr10:96353306 C>T maps to NM_018063.3 R675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr10:96352225 C>T maps to NM_018063.3 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:84350761 G>A maps to NM_133636.2 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr4:84374426 C>G maps to NM_133636.2 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr4:84376713 C>A maps to NM_133636.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:84364762 C>T maps to NM_133636.2 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr4:185941787 G>A maps to NM_001029887.1 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr17:65175037 G>A maps to NM_014877.3 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:65141897 T>C maps to NM_014877.3 V910V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:65197254 G>C maps to NM_014877.3 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr17:65104786 G>A maps to NM_014877.3 F1515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr17:65186415 G>A maps to NM_014877.3 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr17:65156378 G>C maps to NM_014877.3 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr17:65141987 G>A maps to NM_014877.3 F880F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr9:100692794 T>G maps to NM_018437.3 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr9:100693373 C>T maps to NM_018437.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:124794786 G>A maps to NM_152722.4 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr7:92838028 G>A maps to ENST00000453812 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr23:65476068 T>C did not map to a codon.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr23:65486315 G>T did not map to a codon.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr23:65427137 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr23:65476063 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:65390565 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:65392425 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr23:65414977 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr23:65417642 C>G did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:65474893 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:65390419 C>A did not map to a codon.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr23:65415011 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:65480068 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:65392275 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:65409695 C>A did not map to a codon.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr23:65486318 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr23:65474949 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:93778979 G>A maps to NM_001098672.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr11:93796803 G>C maps to NM_001098672.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr11:93819161 T>C maps to NM_001098672.1 Y629Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr15:63930723 C>A maps to ENST00000261887 L3993L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr15:63970198 G>C maps to ENST00000261887 P2305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:63948073 G>A maps to ENST00000261887 L3317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:64010868 T>C maps to ENST00000261887 S1294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:64067651 G>C maps to ENST00000261887 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr15:64017587 A>C maps to ENST00000261887 L1157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr15:63986694 G>A maps to ENST00000261887 Q1766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr15:63908119 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:64017670 G>A maps to ENST00000261887 Q1130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr15:63984689 G>C maps to ENST00000261887 S1917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr15:63922754 G>A maps to ENST00000261887 I4292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr15:63970045 G>A maps to ENST00000261887 I2356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr15:64005027 C>T maps to ENST00000261887 S1510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr15:28361859 G>A maps to NM_004667.4 L4520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr15:28467359 G>A maps to NM_004667.4 G1822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr15:28501376 C>A maps to NM_004667.4 T868T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr15:28460862 C>T maps to NM_004667.4 Q2038Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:28375398 G>A maps to NM_004667.4 R4238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr15:28483900 G>A maps to NM_004667.4 Q1199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr15:28362243 G>A maps to NM_004667.4 V4443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr15:28424336 T>C maps to NM_004667.4 S2990S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr15:28475548 A>G maps to NM_004667.4 N1591N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr15:28493882 C>G did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr15:28408391 G>A maps to NM_004667.4 Q3532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr15:28456241 G>A maps to NM_004667.4 I2325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr15:28420726 C>G maps to NM_004667.4 L3254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr15:28389102 C>T maps to NM_004667.4 L3778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:28459804 G>A maps to NM_004667.4 L2118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr15:28358393 G>C maps to NM_004667.4 L4685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr15:28525374 G>A maps to NM_004667.4 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr15:28413642 C>T maps to NM_004667.4 A3441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr4:89599245 G>C maps to NM_014606.1 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:69785432 C>A maps to NM_022079.2 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:69804184 G>C maps to NM_022079.2 S121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr4:89385091 G>T maps to NM_016323.2 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr4:89352339 T>A maps to NM_017912.3 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr4:89311971 C>A maps to NM_017912.3 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr4:89345854 G>C did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr4:89319307 C>T maps to NM_017912.3 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr16:56969205 C>G maps to NM_014685.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr7:35673356 G>A maps to NM_022373.4 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:193855628 C>T maps to NM_005524.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr3:193854476 G>A maps to NM_005524.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:935113 G>A maps to NM_001142467.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:935176 G>T maps to NM_001142467.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:239147872 C>T maps to NM_018645.4 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:72668265 G>A maps to ENST00000457859 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:80391556 C>T maps to NM_173620.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr17:80391583 C>T maps to NM_173620.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr17:80386487 G>C maps to NM_173620.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr17:80400083 G>A maps to NM_173620.2 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr17:80393671 G>A maps to NM_173620.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:43226865 C>T maps to NM_006460.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr17:43227357 C>T maps to NM_006460.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr8:80677791 G>C maps to NM_001040708.1 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr6:126080648 C>T maps to NM_012259.2 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr6:26093380 C>G maps to NM_000410.3 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr6:26092910 A>T did not map to a codon.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr1:145416380 T>C maps to NM_213653.3 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:145415438 T>C maps to NM_213653.3 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:145416911 T>C maps to NM_213653.3 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:145415417 C>T maps to NM_213653.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:91781701 C>A maps to NM_001017975.3 E980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr1:91812990 A>T maps to NM_001017975.3 L750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr1:91733379 C>A maps to NM_001017975.3 E1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr1:91778937 G>C maps to NM_001017975.3 S1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr1:91781370 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:91742593 C>G maps to NM_001017975.3 G1139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr1:91784767 T>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:91788747 C>T maps to NM_001017975.3 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr3:120393836 C>T did not map to a codon.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr3:120389339 G>A maps to NM_000187.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:81388060 G>C maps to NM_000601.4 S105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr7:81346647 C>G maps to NM_000601.4 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr7:81374403 G>A maps to NM_000601.4 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr7:81355230 T>C maps to NM_000601.4 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr4:3451001 C>T maps to ENST00000511533 G615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr4:3449358 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr4:3449272 G>A maps to ENST00000511533 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr4:3451115 G>A maps to ENST00000511533 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr17:79660898 G>T did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:79668079 C>T maps to NM_004712.4 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr17:79657708 A>G maps to NM_004712.4 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr8:43052997 C>T maps to ENST00000458501 V571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr8:43014176 T>C maps to ENST00000458501 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr8:43048973 T>C maps to ENST00000458501 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr1:210637858 G>A maps to NM_001170580.1 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr1:210522375 C>T maps to NM_001170580.1 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr4:145568049 C>A maps to NM_022475.1 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr4:145567946 G>C maps to NM_022475.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr4:145633194 T>C maps to NM_022475.1 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr14:100123450 C>G maps to NM_001127258.1 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr14:100118592 C>T maps to NM_001127258.1 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr14:100134571 C>T maps to NM_001127258.1 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:222717306 A>G maps to NM_024746.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:222715454 G>T maps to NM_024746.3 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:222717297 C>T maps to NM_024746.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr1:222717231 G>C maps to NM_024746.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr3:108076760 A>G maps to NM_007072.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:108074153 C>G maps to NM_007072.2 S204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:100534135 C>G maps to NM_033055.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr9:97218590 C>G maps to NM_032558.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr7:27570819 G>C maps to NM_152740.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr22:21799327 C>A maps to NM_015094.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr22:21799507 C>T maps to NM_015094.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:62207245 T>C maps to ENST00000394997 C521C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr14:62200932 C>T maps to ENST00000394997 Q321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr14:62207726 G>A maps to ENST00000394997 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr14:62204941 C>T maps to ENST00000394997 R464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr14:62203735 C>G maps to ENST00000394997 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr10:102295783 C>T maps to ENST00000442724 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr10:102296388 G>A maps to ENST00000442724 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:46834523 C>G maps to NM_152795.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr19:46823769 C>A maps to NM_152795.2 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr19:46838172 G>C maps to NM_152795.2 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr19:46815895 C>T maps to NM_152795.2 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr5:175816395 G>A maps to NM_138820.2 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:175816402 C>T maps to NM_138820.2 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr5:175815936 C>T maps to NM_138820.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr11:119003660 C>T maps to NM_198971.1 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:119003646 G>T maps to NM_198971.1 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr11:119005090 C>G maps to NM_198971.1 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr11:118997668 G>A maps to NM_198971.1 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:75172290 C>T maps to NM_005338.4 V923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr7:75178215 A>T maps to NM_005338.4 A793A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr7:75178224 A>C maps to NM_005338.4 T790T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr7:75187037 G>A maps to NM_005338.4 Q501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr12:123340549 G>A maps to NM_003959.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr12:123345273 C>G maps to NM_003959.1 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr12:123338614 C>T maps to NM_003959.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr12:123338614 C>T maps to NM_003959.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:114512679 G>A maps to ENST00000426820 L1029L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:114514629 C>T maps to NM_152696.3 F1066F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr7:139305248 C>T maps to NM_022740.4 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr7:139305245 C>G maps to NM_022740.4 V561V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:139416668 C>T maps to NM_022740.4 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr11:33370176 C>T maps to NM_005734.3 Q827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:33308755 C>T maps to NM_005734.3 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr11:33369460 G>A maps to NM_005734.3 Q736Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:33370304 C>T maps to NM_005734.3 V869V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr11:33308580 G>A maps to NM_005734.3 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr11:33308253 G>A maps to NM_005734.3 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:40886913 C>T maps to NM_144685.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:40889767 G>A maps to NM_144685.3 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr19:40886889 G>A maps to NM_144685.3 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr19:40886784 G>A maps to NM_144685.3 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr19:40890037 G>A maps to NM_144685.3 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr22:19365558 G>T maps to NM_003325.3 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr22:19379665 G>T maps to NM_003325.3 C298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr22:19349416 G>A maps to NM_003325.3 R605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:19418987 C>T maps to NM_003325.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr22:19365414 T>C maps to NM_003325.3 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr22:19384453 C>T maps to NM_003325.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr22:19371165 G>C maps to NM_003325.3 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr22:19384470 C>T did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr22:19341606 G>A maps to NM_003325.3 Q866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr22:19347004 G>C maps to NM_003325.3 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr16:30004528 C>T maps to NM_003609.3 *557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:30005478 C>T maps to NM_003609.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:30005805 C>T maps to NM_003609.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr16:30005484 C>T maps to NM_003609.3 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr16:30005517 C>T maps to NM_003609.3 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr16:30005931 C>T maps to NM_003609.3 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:30006058 G>C maps to NM_003609.3 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr16:30005805 C>A maps to NM_003609.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr16:30005885 C>A maps to NM_003609.3 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr6:26017777 C>A maps to NM_005325.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr6:27834713 C>T maps to NM_005322.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr6:27834977 G>C maps to NM_005322.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr6:27835176 G>C maps to NM_005322.2 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:27835259 C>T maps to NM_005322.2 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr6:26056116 C>T maps to NM_005319.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:26056379 G>A maps to NM_005319.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr6:26056107 C>T maps to NM_005319.3 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr6:26056116 C>T maps to NM_005319.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr6:26056506 G>A maps to NM_005319.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr6:26056191 C>T maps to NM_005319.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr6:26056392 C>T maps to NM_005319.3 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:26056116 C>A maps to NM_005319.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr6:26056215 C>T maps to NM_005319.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr6:26056116 C>G maps to NM_005319.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr6:26234606 T>C maps to NM_005320.2 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr6:26235026 G>A maps to NM_005320.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr6:26156680 G>A maps to NM_005321.2 K21K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr6:26157184 G>C maps to NM_005321.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:26157184 G>A maps to NM_005321.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr6:26107748 T>C maps to NM_005323.3 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr6:26107883 A>G maps to NM_005323.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:26033546 G>A maps to NM_003513.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr6:26124772 C>T maps to NM_003512.3 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:26199438 G>A maps to NM_021065.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr6:26199399 G>C maps to NM_021065.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr6:26217235 C>A maps to NM_021052.2 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:26217567 G>A maps to NM_021052.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:27101227 G>A maps to NM_021064.4 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr6:27101101 C>A maps to NM_021064.4 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr6:27115131 G>A maps to NM_080596.1 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr6:27782212 G>C maps to NM_021066.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr6:27805963 G>A maps to NM_003510.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:27806020 G>A maps to NM_003510.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:27833491 G>A maps to NM_003511.2 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr6:27833413 C>T maps to NM_003511.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:27860614 G>A maps to NM_003514.2 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr6:27860744 G>A maps to NM_003514.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr6:27860795 G>A maps to NM_003514.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr6:25727309 G>A maps to NM_170610.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr6:26043687 G>A maps to NM_021062.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr6:26124026 C>A maps to NM_003526.2 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr6:26123850 C>T maps to NM_003526.2 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr6:26124045 C>T maps to NM_003526.2 K29K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr6:26158444 G>A maps to NM_138720.1 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:26158516 G>A maps to NM_138720.1 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr6:26158660 G>T maps to NM_138720.1 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:26158468 G>A maps to NM_138720.1 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:26158618 C>T maps to NM_138720.1 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr6:26158468 G>A maps to NM_138720.1 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:26184091 G>A maps to NM_003523.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:26184037 G>A maps to NM_003523.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:26184244 C>T maps to NM_003523.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr6:26184244 C>T maps to NM_003523.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr6:26200007 C>A maps to NM_003522.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr6:26216732 T>A maps to NM_003518.3 K47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr6:26216649 G>A maps to NM_003518.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr6:26216598 G>A maps to NM_003518.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:26252141 G>C maps to NM_003524.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr6:26252015 G>A maps to NM_003524.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:26252157 G>T maps to NM_003524.2 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr6:26273274 G>A maps to NM_003525.2 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr6:26273578 A>T maps to NM_003525.2 K126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:26273355 C>G maps to NM_003525.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr6:26273343 G>A maps to NM_003525.2 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr6:27100265 C>G maps to NM_021058.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr6:27100189 C>A maps to NM_021058.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:27114508 C>T maps to NM_080593.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr6:27775612 C>T maps to NM_003519.3 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:27775561 G>C maps to NM_003519.3 Y41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr6:27775576 C>T maps to NM_003519.3 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr6:27775339 G>C maps to NM_003519.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr6:27775471 G>A maps to NM_003519.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr6:27783042 C>T maps to NM_003521.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr6:27782868 G>A maps to NM_003521.2 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr6:27806651 C>T maps to NM_003520.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr6:27806486 G>A maps to NM_003520.3 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr6:27806510 G>A maps to NM_003520.3 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr6:27806474 G>A maps to NM_003520.3 K12K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:27806818 G>A maps to NM_003520.3 *127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr6:27861554 G>A maps to NM_003527.4 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr6:27861410 G>A maps to NM_003527.4 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr6:26032075 C>T maps to NM_003537.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:26045913 G>A maps to NM_003531.2 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr6:26046042 G>A maps to NM_003531.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr6:26197304 C>G maps to NM_003530.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr6:26250647 C>G maps to NM_021018.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr6:26271204 C>A maps to NM_003534.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr6:26271446 G>A maps to NM_003534.2 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr6:27777958 C>T maps to NM_003536.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr6:27777949 C>T maps to NM_003536.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:27778028 G>T maps to NM_003536.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr6:27839871 C>T maps to NM_003533.2 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr6:26188993 C>T maps to NM_003539.3 *104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr6:26188993 C>T maps to NM_003539.3 *104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr6:26247112 G>A maps to NM_003547.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:27107326 G>A maps to NM_003495.2 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr6:27107380 C>T maps to NM_003495.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr6:27107236 C>T maps to NM_003495.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:27840977 C>A maps to NM_003546.2 *104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr6:27840977 C>G maps to NM_003546.2 *104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr1:149859142 G>C maps to NM_175065.2 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:149859298 G>C maps to NM_175065.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:149858826 C>T maps to NM_003517.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr1:149858691 C>G maps to NM_003517.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr1:149857968 G>A maps to NM_003528.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr1:149858067 G>A maps to NM_003528.2 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:149399012 G>T maps to NM_001024599.3 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr1:149783794 C>T maps to ENST00000427880 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr1:149783656 G>A maps to ENST00000427880 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:149785175 G>A maps to NM_001123375.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:228645350 G>A maps to NM_033445.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:228646051 C>T maps to NM_175055.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:14923707 C>G maps to NM_175054.2 *104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr12:14923748 C>T maps to NM_175054.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr6:12125107 C>T maps to NM_002114.2 Q1694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:12164681 G>A maps to NM_002114.2 V2715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:12123623 C>G maps to NM_002114.2 S1199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:12123633 C>T maps to NM_002114.2 L1202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:12123090 C>T maps to NM_002114.2 I1021I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:12124514 C>G maps to NM_002114.2 S1496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:12125641 C>T maps to NM_002114.2 R1872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr6:12164327 C>T maps to NM_002114.2 T2597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr6:12120591 C>T maps to NM_002114.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr6:12124950 G>A maps to NM_002114.2 Q1641Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr6:12122274 G>A maps to NM_002114.2 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr6:143093574 A>C maps to NM_006734.3 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr6:143074786 C>T maps to NM_006734.3 A2266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr6:143095263 C>G maps to NM_006734.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:42048497 G>A maps to NM_024503.3 N657N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:42049979 G>T maps to NM_024503.3 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:42046439 G>C maps to NM_024503.3 V1343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:42049046 G>C maps to NM_024503.3 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:42049172 C>T maps to NM_024503.3 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr1:42047924 G>A maps to NM_024503.3 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:41979190 G>A maps to NM_024503.3 Q1901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr1:42041252 C>T maps to NM_024503.3 Q1723Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr10:71075754 G>A maps to NM_033496.2 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr10:71136782 G>A maps to ENST00000439900 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr10:71129054 C>T maps to ENST00000439900 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr10:71128326 G>A maps to ENST00000439900 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr10:71144658 G>A maps to ENST00000439900 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr10:71144089 G>A maps to ENST00000439900 E559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr2:75116557 C>G maps to NM_000189.4 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr2:75109300 A>T maps to NM_000189.4 K592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr2:75115174 C>T maps to NM_000189.4 Q789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr5:176316679 C>T maps to NM_002115.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr5:176314050 T>A maps to NM_002115.2 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:176309064 G>C maps to NM_002115.2 S706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr5:176308337 C>G maps to NM_002115.2 V864V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr5:176314550 G>A maps to NM_002115.2 Q501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr10:70992646 C>T maps to NM_025130.3 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:70992595 G>A maps to NM_025130.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr10:71010044 G>C did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr10:71008377 G>A maps to NM_025130.3 Q488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr10:71026396 G>T maps to NM_025130.3 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr10:71026408 C>T maps to NM_025130.3 R884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr19:37853563 C>T maps to NM_181786.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:37853219 C>T maps to NM_181786.2 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr6:29913230 G>T maps to ENST00000376806 *372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr6:29913230 G>C maps to ENST00000376806 *372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr6:29912275 G>C did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr6:31324022 C>T maps to ENST00000428231 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:31323358 C>T maps to ENST00000428231 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:31323369 C>G did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr6:31322893 C>T maps to ENST00000428231 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr6:31324874 C>A maps to ENST00000428231 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:31239078 G>A maps to ENST00000383329 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:31239457 C>T maps to ENST00000383329 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:31237267 A>C did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr6:31239460 C>G maps to ENST00000383329 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:32917583 G>A maps to NM_006120.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr6:32908578 G>A maps to NM_002118.4 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr6:32906743 T>C did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr6:32903328 C>A maps to NM_002118.4 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr6:32903400 C>T maps to NM_002118.4 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr6:32905009 C>T maps to NM_002118.4 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:32977304 G>C maps to NM_002119.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:32977304 G>A maps to NM_002119.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:32784729 C>T did not map to a codon.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr6:33036805 G>C maps to NM_033554.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr6:32630008 G>T maps to ENST00000374943 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:32634315 C>T maps to ENST00000374943 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:30457337 C>G maps to NM_005516.5 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:29694182 G>T maps to NM_018950.2 *347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr6:29694775 C>A maps to NM_001098479.1 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr6:29797698 G>A maps to ENST00000376828 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr21:38126564 G>A maps to NM_000411.5 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr21:38139582 C>T maps to NM_000411.5 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr21:38302560 G>C maps to NM_000411.5 S390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr17:53345370 C>T maps to NM_002126.4 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:221053336 C>T maps to NM_021958.3 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:221053720 C>T maps to NM_021958.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:221053786 G>C maps to NM_021958.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:221057811 C>T maps to NM_021958.3 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:30137128 C>A maps to NM_178581.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr20:30132834 G>T maps to NM_178581.1 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr8:28827754 G>T maps to ENST00000444075 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr8:28876349 C>G maps to ENST00000444075 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr1:186022144 C>T maps to NM_031935.2 L2213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr1:186106800 G>A did not map to a codon.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:186114896 G>A maps to NM_031935.2 W4817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:186088321 G>A did not map to a codon.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr1:186034487 C>T maps to NM_031935.2 H2544H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr1:185966559 G>C did not map to a codon.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr1:186043956 C>T maps to NM_031935.2 R2742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:186037085 G>A maps to NM_031935.2 W2609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr1:186038810 G>A maps to NM_031935.2 Q2632Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:186008051 C>A maps to NM_031935.2 A1981A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:186076086 G>A maps to NM_031935.2 V3614V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr1:186014961 C>T maps to NM_031935.2 G2149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr1:186158667 C>T maps to NM_031935.2 P5522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:186038816 C>G maps to NM_031935.2 L2634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr1:186107003 C>A maps to NM_031935.2 T4608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:186022985 C>A maps to NM_031935.2 R2244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr1:186056409 A>T maps to NM_031935.2 I3036I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr1:186024540 C>T maps to NM_031935.2 T2293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:186047317 A>C maps to NM_031935.2 G2855G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:186057736 G>C did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:186094826 A>G maps to NM_031935.2 T4197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr1:185956591 G>A maps to NM_031935.2 Q988Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:185704087 G>A maps to NM_031935.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:185892708 C>G maps to NM_031935.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:186026400 G>T maps to NM_031935.2 E2394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:186044019 C>T maps to NM_031935.2 Q2763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:186050379 G>T maps to NM_031935.2 E2881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:186121954 G>A maps to NM_031935.2 V4990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr1:186037080 C>A maps to NM_031935.2 I2607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr1:186088377 C>T maps to NM_031935.2 V3968V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr1:186043952 C>T maps to NM_031935.2 T2740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr1:186136069 T>C maps to NM_031935.2 C5190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr1:186017915 T>A maps to NM_031935.2 C2174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr1:185833600 G>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr1:186099684 A>C maps to NM_031935.2 P4362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr15:77770686 G>T maps to NM_018200.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr15:77750760 G>A maps to NM_018200.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr15:77759616 G>T maps to NM_018200.2 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr19:3574457 G>C maps to NM_006339.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr12:66308891 T>C maps to NM_003484.1 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr13:31035516 C>A maps to NM_002128.4 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr4:174254743 G>A maps to NM_002129.3 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr4:174254743 G>A maps to NM_002129.3 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr4:174253311 C>T maps to NM_002129.3 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMW-01A-11D-A42E-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:34329949 C>G maps to NM_145205.4 S53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:24134630 G>T maps to NM_000191.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr6:55378865 G>A maps to NM_019036.2 H204H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:74645874 C>T maps to NM_000859.2 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr5:74654523 G>T maps to NM_000859.2 E677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:43295897 C>T maps to NM_002130.6 Q287Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr5:43295935 G>A maps to NM_002130.6 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:120298216 C>T maps to NM_005518.3 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr1:26800008 G>T maps to NM_005517.3 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr23:80373934 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr22:35660905 C>T maps to NM_001003681.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:1073671 G>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr19:1080502 G>C maps to NM_012292.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:1068606 G>A maps to NM_012292.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr19:1080304 G>A maps to NM_012292.2 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr19:1079964 G>T maps to NM_012292.2 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr5:143200099 G>C maps to NM_021182.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:162894720 G>A maps to NM_001142556.1 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr5:162909656 G>A maps to NM_001142556.1 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:4556894 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr16:4559636 G>C maps to NM_001127205.1 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr16:4557744 C>G maps to NM_001127205.1 S79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr5:173491270 C>T maps to NM_015980.3 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr5:173534468 C>T maps to NM_015980.3 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr10:124896931 C>T maps to NM_001105574.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:124896739 C>T maps to NM_001105574.1 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:73132156 G>A maps to NM_001002032.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:1741916 G>A maps to ENST00000382711 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr16:1741901 G>C maps to ENST00000382711 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr12:121431981 G>A maps to NM_000545.5 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:121438964 C>A maps to NM_000545.5 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr12:121416585 G>C maps to NM_000545.5 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr12:121432059 C>T maps to NM_000545.5 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr17:36093622 A>G maps to NM_000458.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr17:36104533 G>A maps to NM_000458.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr17:36104668 G>A maps to NM_000458.2 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr20:43030113 G>A maps to ENST00000338692 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:43057089 A>G maps to ENST00000338692 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr20:43056984 C>T maps to ENST00000338692 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr20:43052973 C>T maps to NM_178850.1 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr8:76465275 G>A did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr8:76468214 A>T did not map to a codon.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr8:76456043 A>T did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr8:76465353 T>C maps to NM_004133.4 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr2:138724672 G>A maps to NM_001024074.2 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr2:138758530 C>T maps to NM_006895.2 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr2:138738933 A>G maps to NM_001024075.1 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr5:137089587 G>C maps to NM_006805.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr5:137089491 C>A maps to NM_006805.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr5:137089347 G>C maps to NM_006805.3 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr5:137089326 G>A maps to NM_006805.3 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr12:54675243 G>A maps to NM_031157.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr12:54675243 G>A maps to NM_031157.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr7:26232147 C>T maps to NM_031243.2 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr7:26237280 C>T maps to NM_031243.2 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr5:177637273 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:21699231 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr1:12908073 G>C maps to NM_001013631.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr1:12907497 C>G maps to NM_001013631.1 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:12907696 G>C maps to NM_001013631.1 S149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:83278510 C>T maps to NM_031370.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr4:83280672 G>C maps to NM_031370.2 S137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr10:43883161 A>C maps to NM_001098204.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:100667668 G>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:100667414 T>A did not map to a codon.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr9:86586584 A>C did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr9:86586834 C>A maps to NM_031262.2 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:86585191 C>A maps to NM_031262.2 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr19:39334701 G>A maps to ENST00000221419 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:39329038 C>A maps to ENST00000221419 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:8509965 G>T maps to NM_005968.3 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:8527460 C>G maps to NM_005968.3 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:8533686 C>T maps to NM_005968.3 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr19:8550571 C>T maps to NM_005968.3 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr19:8551105 G>T maps to NM_005968.3 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:23637375 G>A maps to ENST00000414299 Y495Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr19:41812427 G>A maps to NM_007040.3 G843G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:41808693 C>T maps to NM_007040.3 P604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr19:41778074 G>A maps to NM_007040.3 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr19:41782118 C>T maps to NM_007040.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:62483064 G>A maps to NM_001079559.1 F690F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr11:62491785 G>A maps to NM_001079559.1 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr2:38791379 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr2:38804674 C>G did not map to a codon.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr5:78671999 T>C maps to NM_004272.3 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr15:83532987 C>A maps to NM_199330.1 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr15:83527800 C>A maps to NM_199330.1 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr19:19049287 G>A maps to NM_004838.3 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:19049693 C>T did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:60336746 G>T maps to NM_015888.4 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:60297858 C>T maps to NM_015888.4 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr8:42837794 G>A maps to NM_032410.3 E449E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr8:42852738 T>C maps to NM_032410.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:150679154 C>G maps to NM_032132.4 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:150676595 G>A maps to NM_032132.4 Q316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:150679027 C>A did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr1:150679138 G>A maps to NM_032132.4 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:150689681 G>T maps to NM_032132.4 S37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:150689729 G>C maps to NM_032132.4 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr22:30494893 G>A maps to NM_152510.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr7:27135405 G>A maps to NM_005522.4 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr7:27237852 C>T maps to NM_000522.4 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr7:27142022 G>A maps to NM_006735.3 Q33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr7:27187113 G>A maps to NM_024014.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:46608134 G>A maps to NM_002144.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:46607196 G>A maps to NM_002144.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr17:46607196 G>A maps to NM_002144.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:46805664 C>T maps to NM_006361.5 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:46805514 A>G maps to NM_006361.5 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr17:46622153 C>T maps to NM_002145.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:46628331 C>T maps to NM_002146.4 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr17:46628307 G>A maps to NM_002146.4 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr17:46673861 G>A maps to NM_018952.4 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:46690569 C>T maps to NM_024016.3 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:46690719 G>A maps to NM_024016.3 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr17:46691982 G>A maps to NM_024016.3 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr17:46690725 G>A maps to NM_024016.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:54367562 G>T maps to NM_014212.3 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr12:54338862 G>A maps to NM_017410.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr12:54333277 G>A maps to NM_017410.2 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:54448005 G>A maps to NM_153633.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:54423559 C>T maps to NM_004503.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:54422346 C>T maps to NM_004503.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:54423592 C>T maps to NM_004503.3 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr12:54403394 G>A maps to NM_022658.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr2:177054695 G>A maps to ENST00000331462 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr2:176983680 G>C did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:176965481 C>A maps to NM_021193.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:176958256 C>T maps to NM_000523.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr2:176958226 G>T maps to NM_000523.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr2:177034234 C>A maps to NM_006898.4 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr2:177017651 G>A maps to NM_014621.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:177016456 G>A maps to NM_014621.2 Q32Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:177017630 G>A maps to NM_014621.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:176995372 C>T maps to NM_019558.3 Y93Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:72094455 G>A maps to NM_005143.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:72094737 G>A maps to NM_005143.3 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:21071502 G>A maps to NM_016287.3 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:21076329 C>A maps to NM_016287.3 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr2:10563185 C>T maps to NM_002149.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:40149689 C>T maps to NM_016257.2 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:122287615 G>A maps to NM_002150.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr4:175443098 C>T maps to NM_000860.4 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:35540382 T>A maps to NM_182983.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr19:35551677 C>T maps to NM_182983.2 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr16:72110370 C>G maps to ENST00000228226 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:72110730 G>A maps to ENST00000228226 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:72107849 C>G maps to ENST00000228226 S59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr16:72110374 C>T maps to ENST00000228226 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr16:72107862 C>A maps to ENST00000228226 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr16:72107849 C>A maps to ENST00000228226 S59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr23:133609214 G>A did not map to a codon.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr10:100202939 G>A maps to NM_000195.2 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr10:100177392 A>C maps to NM_000195.2 T677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:100185613 C>T maps to NM_000195.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr10:100195122 C>A maps to NM_000195.2 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr10:100185672 G>A maps to NM_000195.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:148847596 G>C maps to NM_032383.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr3:148889890 C>G maps to NM_032383.3 S966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr3:148847536 G>A maps to NM_032383.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr3:148876569 G>A maps to NM_032383.3 E603E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr22:26860539 G>A maps to NM_022081.4 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr22:26866710 G>A maps to NM_022081.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr22:26868342 G>A maps to NM_022081.4 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr22:26862216 C>T maps to NM_022081.4 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr11:18301458 G>A maps to NM_181507.1 C1120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:18309161 G>A maps to NM_181507.1 I879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:18322408 C>T maps to NM_181507.1 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr10:103826019 C>T maps to NM_024747.4 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr10:103825278 C>T maps to NM_024747.4 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr10:103827141 C>G maps to NM_024747.4 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr10:100249920 C>G maps to NM_021828.4 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr10:100995298 G>A maps to NM_021828.4 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr10:100242423 G>A maps to NM_021828.4 Q528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:6461460 C>T maps to NM_000613.2 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr11:533468 G>T maps to NM_005343.2 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:532641 G>A maps to NM_005343.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr11:63320519 C>T maps to NM_017878.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr11:63320462 C>T maps to NM_017878.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr11:63257770 G>C maps to NM_054108.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:49658060 G>C maps to NM_002152.2 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr19:49657933 C>G maps to NM_002152.2 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:49657669 G>T maps to NM_002152.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:49656910 G>A maps to NM_002152.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:49658053 C>T maps to NM_002152.2 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr3:186383943 C>T maps to NM_000412.2 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr3:186395191 C>T maps to NM_000412.2 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr3:11300830 T>G maps to NM_001098211.1 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:11301167 C>T maps to NM_001098211.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:11300812 G>A maps to NM_001098211.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:175110436 C>T maps to NM_001131055.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr5:175111303 C>T maps to NM_001131055.1 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr5:175111276 G>T maps to NM_001131055.1 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr5:175110580 C>T maps to NM_001131055.1 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr20:60791270 G>A maps to ENST00000317393 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr20:60791550 G>A maps to ENST00000317393 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr20:60794804 G>C maps to ENST00000317393 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr20:60793657 G>A maps to ENST00000317393 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:60794804 G>T maps to ENST00000317393 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr18:22040841 T>C maps to NM_021624.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:152193079 G>C maps to NM_001009931.1 S342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:152193966 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:152187696 G>A maps to NM_001009931.1 H2136H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr1:152187630 G>A maps to NM_001009931.1 R2158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr1:152187646 G>C maps to NM_001009931.1 S2153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr1:152188365 G>A maps to NM_001009931.1 H1913H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:152191809 G>A maps to NM_001009931.1 H765H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:152195630 C>T maps to NM_001009931.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr1:152192210 G>A maps to NM_001009931.1 Q632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:152188432 G>C maps to NM_001009931.1 S1891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:152190990 G>A maps to NM_001009931.1 G1038G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr1:152192622 G>A maps to NM_001009931.1 H494H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr8:99118184 G>A maps to NM_005836.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:87380808 G>A maps to NM_012262.3 Q30Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr4:11401131 C>T maps to NM_005114.2 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:22826362 C>T maps to NM_006043.1 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr16:22926364 C>T maps to NM_006043.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr16:22926557 G>A maps to NM_006043.1 W260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr17:13503915 G>A maps to NM_006042.1 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr17:14248386 G>A maps to NM_006041.1 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr17:14204870 C>G maps to NM_006041.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr17:14205044 C>T maps to NM_006041.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr16:26146938 G>A maps to NM_006040.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr16:26147160 C>T maps to NM_006040.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr6:114378864 C>T maps to NM_153612.3 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr6:114378489 C>T maps to NM_153612.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr6:114383970 G>A maps to NM_153612.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:132091163 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:131762711 T>A did not map to a codon.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr13:96743169 C>T maps to NM_153456.2 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr13:96743175 C>G maps to NM_153456.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr22:29140640 G>A maps to NM_172002.3 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr22:29153141 G>A maps to NM_172002.3 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr1:209905859 G>A maps to NM_005525.2 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr19:5687303 G>A maps to NM_198706.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr19:5687577 C>T maps to NM_198706.1 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:5687330 G>A maps to NM_198706.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr19:5687342 G>A maps to NM_198706.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr19:5687832 G>A maps to NM_198706.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr16:67470803 G>A maps to NM_000196.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr17:40705229 G>A maps to NM_000413.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr17:40705873 C>T maps to NM_000413.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr23:53459193 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:53459338 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr23:53460770 A>G did not map to a codon.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr4:88226450 A>T maps to NM_178135.3 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:49334954 C>T maps to NM_016246.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:49316712 C>T maps to NM_016246.2 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr19:49334930 C>T maps to NM_016246.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr19:49316805 G>A maps to NM_016246.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr16:82131776 C>T maps to NM_002153.2 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr16:82131830 C>T maps to NM_002153.2 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr16:82069214 G>C maps to NM_002153.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr9:99017207 G>C maps to NM_000197.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr12:57175941 G>A maps to NM_003725.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:57181044 C>T maps to NM_003725.2 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:162762470 A>T maps to NM_016371.2 K20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:162767597 G>A maps to NM_016371.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr6:33173673 G>A maps to NM_014234.3 Q212Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr1:120056706 C>T maps to ENST00000235547 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr1:120054243 C>G maps to ENST00000235547 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:120056979 C>T maps to ENST00000235547 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:119964492 T>C maps to NM_000198.3 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SU-01A-31D-A391-08 chr1:119965137 G>A maps to NM_000198.3 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr16:30997086 C>T maps to NM_025193.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr9:115171289 C>T maps to NM_032303.4 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr8:145535420 C>T maps to NM_005526.2 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr8:145535453 C>A maps to NM_005526.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr8:145535831 C>A maps to NM_005526.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:122733618 G>A maps to NM_004506.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:122752618 G>A maps to NM_004506.3 Q425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:122733609 G>A maps to NM_004506.3 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr21:45053254 G>A maps to NM_007031.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:56557374 T>G maps to NM_001080439.1 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:16268237 C>T maps to NM_032855.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr14:102551676 C>T maps to NM_001017963.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr14:102549997 C>T maps to NM_001017963.2 K579K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:102552648 G>A maps to NM_001017963.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr14:102551298 C>A maps to NM_001017963.2 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:102605689 G>T maps to NM_001017963.2 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr14:102605681 C>T maps to NM_001017963.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr14:102552187 C>A maps to NM_001017963.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:102551247 C>A maps to NM_001017963.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr14:102548107 C>A maps to NM_001017963.2 E836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr6:44217153 C>A maps to NM_007355.2 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr6:44216417 C>T maps to NM_007355.2 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr6:44221298 C>T maps to NM_007355.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:44219207 G>T maps to NM_007355.2 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:44216417 C>T maps to NM_007355.2 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr6:44217223 G>A maps to NM_007355.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:44219876 C>G maps to NM_007355.2 S535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr6:44218173 G>A maps to NM_007355.2 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:104336351 G>A maps to NM_003299.1 K474K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:104336507 G>A maps to NM_003299.1 Q526Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr12:104327861 A>G maps to NM_003299.1 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr12:104327816 C>T maps to NM_003299.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:104337523 G>A maps to NM_003299.1 K633K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr10:118458187 G>A maps to NM_025015.2 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr10:118435908 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr10:118451882 G>A maps to NM_025015.2 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr10:118434435 G>C maps to NM_025015.2 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr20:3730478 C>T maps to NM_052970.4 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr20:3728895 G>A maps to NM_052970.4 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr20:3726566 G>A maps to NM_052970.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr20:3728901 C>A maps to NM_052970.4 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr20:3723035 G>T maps to NM_052970.4 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr6:31785455 T>C maps to NM_005345.5 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr6:31785263 C>T maps to NM_005345.5 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr6:31785218 C>T maps to NM_005345.5 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr6:31797430 G>A maps to NM_005346.4 K568K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:65009222 C>T maps to NM_021979.3 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr14:65007941 C>T maps to NM_021979.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr14:65009309 C>T maps to NM_021979.3 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr14:65008895 G>A maps to NM_021979.3 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:132424171 C>T maps to NM_002154.3 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:132424225 C>G maps to NM_002154.3 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr5:132424775 C>T maps to NM_002154.3 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr4:128751931 C>G maps to ENST00000438626 S799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr4:128715243 A>G maps to ENST00000438626 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr4:128703774 G>T maps to ENST00000438626 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr4:128716921 G>C did not map to a codon.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr4:128703773 C>T maps to ENST00000438626 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr9:127998870 C>T maps to NM_005347.4 *655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr1:161494966 G>A maps to NM_002155.3 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr1:161494981 C>A maps to NM_002155.3 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr1:161494742 G>T maps to NM_002155.3 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr1:161495767 C>G maps to NM_002155.3 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr11:122931933 C>T maps to NM_006597.3 Q33Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:122931882 C>T maps to NM_006597.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:122930370 G>A maps to NM_006597.3 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr11:122928486 G>A maps to NM_006597.3 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:122928456 A>G maps to NM_006597.3 I642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr11:122930537 C>A maps to NM_006597.3 E255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr5:137892239 G>C maps to NM_004134.6 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr5:137892269 C>G maps to NM_004134.6 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr5:137895692 G>A maps to NM_004134.6 Q424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr11:111784273 G>A maps to NM_001541.3 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr5:53751950 C>G maps to NM_006308.2 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr12:119631569 C>T maps to NM_014365.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:122459617 C>T maps to NM_024610.4 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr3:122478186 G>A maps to NM_024610.4 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr19:55776710 C>A maps to NM_012267.4 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:55773976 C>G maps to NM_012267.4 *360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:198367981 G>A maps to NM_002157.2 *103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr1:22176548 G>A maps to NM_005529.5 L2477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:22178311 A>T maps to NM_005529.5 T2326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:22176611 C>G maps to NM_005529.5 L2456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:22165876 G>A maps to NM_005529.5 I3292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:22203043 G>A maps to NM_005529.5 V929V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:22157764 G>A maps to NM_005529.5 L3835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr1:22158274 G>C maps to NM_005529.5 S3741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:22178282 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr1:22181904 C>T maps to NM_005529.5 E1963E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr1:22174478 G>A maps to NM_005529.5 V2615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr1:22183798 G>A maps to NM_005529.5 F1791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr1:22150833 G>A maps to NM_005529.5 I4260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:22206971 G>T maps to NM_005529.5 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:22181826 C>T maps to NM_005529.5 W1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:22205150 G>C maps to NM_005529.5 S826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:22214527 G>A maps to NM_005529.5 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:22211108 G>A maps to NM_005529.5 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:22216513 G>A maps to NM_005529.5 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:22183586 C>G maps to NM_005529.5 L1832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr13:31711652 G>A maps to NM_006644.2 N793N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr13:31728799 G>C maps to NM_006644.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr13:31719798 T>C maps to NM_006644.2 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr23:135594160 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr23:135593752 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr23:135591294 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr23:135579900 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:135593695 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:135592319 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr23:135593381 G>T did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr23:135593381 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr23:135592282 G>T did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:63257012 C>A maps to NM_000524.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr5:63256874 G>A maps to NM_000524.2 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr5:63257087 G>A maps to NM_000524.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr5:63256841 C>T maps to NM_000524.2 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr5:63256508 C>A maps to NM_000524.2 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr6:78172399 T>A maps to NM_000863.1 K241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:87725855 C>T maps to NM_000865.2 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr6:87725384 C>G maps to NM_000865.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr6:87726068 C>T maps to NM_000865.2 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:88040997 T>C maps to NM_000866.3 *367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr3:88040156 A>G maps to NM_000866.3 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr13:47469987 T>C maps to NM_000621.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr13:47409472 G>A maps to NM_000621.3 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr2:231978476 G>A maps to NM_000867.4 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:231973558 G>C maps to NM_000867.4 S373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr2:231974049 C>T maps to NM_000867.4 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr23:114141689 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr23:114141243 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr11:113857499 C>A maps to NM_213621.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:113815413 C>T maps to NM_006028.3 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:113775662 C>G maps to NM_006028.3 S3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:183756392 C>T maps to NM_001145143.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr3:183824030 C>G maps to NM_182589.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr5:147889527 G>A maps to NM_001040173.2 N189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr5:147928313 C>T maps to NM_001040173.2 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr7:154875956 G>A maps to NM_024012.2 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr7:154863040 G>A maps to NM_024012.2 T144T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-XF-AAN3-01A-11D-A42E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:19992500 G>A maps to NM_000871.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr1:19992446 G>A maps to NM_000871.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:19992590 C>T maps to NM_000871.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr10:92617281 C>G maps to NM_019859.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr10:92508998 C>A maps to NM_019859.3 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr10:124249039 G>A maps to NM_002775.4 K225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:74757144 G>A maps to NM_013247.4 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:74757144 G>A maps to NM_013247.4 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:74757254 C>G maps to NM_013247.4 S41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr2:74757812 C>G maps to NM_013247.4 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr4:8284260 G>A maps to NM_053044.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr4:8284197 C>T maps to NM_053044.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr8:38831862 C>G maps to NM_153692.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr8:38831910 C>G maps to NM_153692.3 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr4:3208287 C>T maps to NM_002111.6 I1928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr4:3208580 C>G maps to NM_002111.6 L1982L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:3176446 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:3213723 G>A maps to NM_002111.6 K2161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:3211630 G>T maps to NM_002111.6 V2123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr4:3208557 C>T maps to NM_002111.6 Q1975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr4:3131757 C>T maps to NM_002111.6 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr4:3237488 C>T maps to NM_002111.6 L2923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr4:3117908 C>G maps to NM_002111.6 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr4:3237302 G>A maps to NM_002111.6 V2861V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr4:3148630 C>G maps to NM_002111.6 S1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr4:3235029 C>G maps to NM_002111.6 L2802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr4:3174750 C>A maps to NM_002111.6 G1353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr4:3208284 G>C maps to NM_002111.6 L1927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr21:33297039 A>T maps to NM_014586.1 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr21:33296929 C>T maps to NM_014586.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr7:48015278 A>G maps to NM_004507.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr7:48004978 G>A maps to NM_004507.2 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:48018031 G>A maps to NM_004507.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:53575137 G>A did not map to a codon.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr23:53672364 G>A did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:53587225 C>T did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr23:53603878 T>C did not map to a codon.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr23:53631582 G>C did not map to a codon.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr23:53620498 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr23:53578102 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr23:53578135 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr23:53578271 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:53630452 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr23:53619389 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr23:53654790 A>C did not map to a codon.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr23:53561611 C>T did not map to a codon.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr23:53634539 C>G did not map to a codon.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr23:53602722 C>T did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:53575133 G>A did not map to a codon.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr23:53611262 G>C did not map to a codon.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr23:53574941 A>G did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr23:53617424 C>G did not map to a codon.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr23:53565382 G>A did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:53577925 G>C did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr23:53631593 G>A did not map to a codon.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr23:53615407 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:53607867 C>G did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:53621516 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr23:53592081 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:53674348 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr23:53595717 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr23:53564648 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr23:53611144 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:53602709 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr23:53564590 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:53576079 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr23:53602628 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr23:53620514 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:111088077 G>A maps to NM_001040107.1 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:50340339 G>T maps to NM_153281.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:50331092 G>C maps to NM_003549.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr3:50331101 G>A maps to NM_003549.2 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SU-01A-31D-A391-08 chr7:123508587 C>T maps to NM_012269.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr16:70917862 G>A maps to NM_032821.2 A3312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr16:70884497 G>A maps to NM_032821.2 I4167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr16:70896051 C>T maps to NM_032821.2 V3891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr16:70934908 C>A maps to NM_032821.2 E3015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr16:71220683 C>A maps to NM_032821.2 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr16:70841856 C>A maps to NM_032821.2 E4997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:70843805 C>T maps to NM_032821.2 L4920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN8-01A-11D-A42E-08 chr16:70954658 T>C maps to NM_032821.2 R2539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr16:71127743 G>A maps to NM_032821.2 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:125769667 G>A maps to NM_001134793.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr11:118918693 G>A maps to NM_001130991.1 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:9628346 C>T maps to NM_001039613.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr2:9616124 C>T maps to NM_001039613.1 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:94984838 C>T maps to ENST00000375660 R1225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:95033890 G>T maps to ENST00000375660 S348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr1:220318849 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:88732609 G>T maps to NM_004967.3 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr4:88732623 C>T maps to NM_004967.3 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr6:82941440 G>A maps to NM_015525.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr6:82935192 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:82936932 T>G maps to NM_015525.2 G210G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G2-AA3D-01A-11D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr6:82909957 G>A maps to NM_015525.2 F975F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr6:82950047 G>A maps to NM_015525.2 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr7:8196771 G>A maps to ENST00000422063 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:203650666 G>C maps to NM_138468.4 S436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr2:203653658 G>C maps to NM_138468.4 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr2:203684591 C>T maps to NM_138468.4 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr19:10395088 G>A maps to NM_000201.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr19:10395564 C>G maps to NM_000201.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr17:62082628 C>A maps to NM_001099789.1 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr17:62080229 C>T maps to NM_001099789.1 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr19:10445850 G>T maps to NM_002162.3 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:10398056 G>A maps to NM_001544.3 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:10403672 G>C did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:10403750 G>T maps to NM_003259.3 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:10405104 C>A maps to NM_003259.3 C673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr19:10406169 G>A maps to NM_003259.3 S793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:52876708 C>T maps to NM_016513.4 E450E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr6:52883193 G>C maps to NM_016513.4 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:6285270 G>A maps to NM_012405.3 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr21:45656810 C>A maps to ENST00000400379 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:73017051 G>A maps to NM_001545.1 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:73016474 G>A maps to NM_001545.1 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr17:73016591 A>T maps to NM_001545.1 K126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:30193213 C>T maps to NM_002165.2 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr20:30193327 C>G maps to NM_002165.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr20:30193246 G>A maps to NM_002165.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr20:30193234 C>T maps to NM_002165.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr10:94274784 G>A maps to NM_004969.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:209108166 G>A maps to NM_005896.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr15:90633750 G>C maps to NM_002168.2 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr15:90630732 C>T maps to NM_002168.2 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr15:78449892 C>T maps to NM_005530.2 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr15:78453947 C>T maps to NM_005530.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr15:78461300 C>G maps to NM_005530.2 S352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr20:2640191 C>T maps to NM_006899.2 K350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:153052949 T>A did not map to a codon.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr10:1089292 G>C maps to NM_004508.2 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr10:1070540 C>G maps to NM_033261.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr8:39806666 G>C did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr8:39872886 G>C maps to NM_194294.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr8:39871116 G>T maps to NM_194294.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr23:148564457 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:148571930 A>G did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:148586588 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:148568537 C>A did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:13264011 G>A maps to NM_004907.2 Q4Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr19:13264164 C>G maps to NM_004907.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr6:30712139 G>A maps to NM_003897.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr18:44682581 G>C maps to NM_016097.3 S72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr18:44702591 G>T maps to NM_016097.3 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr1:181058383 G>T maps to NM_016545.4 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr12:6664904 C>G maps to NM_001193457.1 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr12:6664955 C>G maps to NM_001193457.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:6664601 C>T maps to NM_001193457.1 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr12:6664484 C>T maps to NM_001193457.1 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:159021524 G>A maps to ENST00000295809 Q574Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:158984608 C>T maps to ENST00000295809 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr14:94582169 G>A maps to ENST00000448882 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr14:94595893 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr19:18288575 T>A did not map to a codon.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr1:27992963 G>A maps to NM_022873.2 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr2:163167352 G>A maps to NM_022168.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:163133411 C>A maps to NM_022168.2 E697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:163144770 C>T maps to NM_022168.2 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr10:91066853 C>T maps to NM_001547.4 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr10:91099495 C>T maps to NM_001549.4 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr10:91099410 C>G maps to NM_001549.4 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr10:91099692 G>A maps to NM_001549.4 Q427Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:319921 C>T maps to NM_021034.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr12:25679783 G>A maps to NM_001145728.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr9:21239748 G>T maps to NM_002172.2 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr9:21227647 G>C maps to NM_021268.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:21384830 G>A maps to NM_000605.3 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr9:21166299 G>C maps to NM_002175.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr9:21166191 G>A maps to NM_002175.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr9:21187496 G>A maps to NM_021068.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr9:21350637 C>T maps to NM_021002.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr9:21202053 G>C maps to NM_021057.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr9:21201948 C>T maps to NM_021057.2 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr9:21202044 G>A maps to NM_021057.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr9:21201762 C>G maps to NM_021057.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr21:34721713 C>G maps to NM_000629.2 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr21:34717649 C>T maps to NM_000629.2 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr21:34717655 C>T maps to NM_000629.2 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr21:34635355 G>T maps to NM_207585.1 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr21:34635352 G>T maps to NM_207585.1 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr9:21481315 C>T maps to NM_176891.4 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr6:137525537 G>A maps to NM_000416.2 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr6:137519302 G>A maps to NM_000416.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr6:137519209 C>T maps to NM_000416.2 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr21:34804514 C>G maps to ENST00000381995 S217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr21:34787220 C>T maps to ENST00000381995 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr9:27524618 C>T maps to NM_020124.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr9:27524639 C>T maps to NM_020124.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:21141382 G>A maps to NM_002177.1 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:21141550 G>A maps to NM_002177.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:112112291 G>T maps to NM_001007245.2 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr7:112112272 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr7:112096061 G>T maps to NM_001007245.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr3:50326367 C>A maps to ENST00000336089 E462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr3:50327673 G>A maps to ENST00000336089 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:129214428 C>A maps to NM_052985.2 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr3:129196908 C>T maps to NM_052985.2 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:129231225 C>T maps to NM_052985.2 P1037P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr3:129182457 C>T maps to NM_052985.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr16:1613997 C>T maps to NM_014714.3 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:1575299 G>A maps to NM_014714.3 F932F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr16:1576757 C>T maps to NM_014714.3 K813K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr16:1573575 G>A maps to NM_014714.3 F1132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:27700948 C>T maps to NM_015662.1 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr2:27703992 G>A maps to NM_015662.1 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:118416127 G>C maps to NM_020153.3 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr11:118425975 G>A maps to NM_020153.3 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:42264601 C>G maps to NM_016004.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:27036446 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr9:26984495 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr9:27016984 A>G maps to NM_025103.2 Q290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:159995412 G>A maps to ENST00000483754 R799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr12:110618348 A>G maps to NM_014055.3 Q437Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:110565214 C>T maps to NM_014055.3 D10D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr13:21148538 G>T maps to NM_175605.3 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr13:21175889 C>T maps to NM_175605.3 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr13:21265281 G>T maps to NM_175605.3 E824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr13:21157159 T>G did not map to a codon.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr23:69353900 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:69353912 A>G did not map to a codon.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr15:65621841 C>T maps to NM_004884.3 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr15:65625613 C>T maps to NM_004884.3 Q321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr15:65667513 C>T maps to NM_004884.3 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr15:65667593 C>A maps to NM_004884.3 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr15:65681730 G>T maps to NM_020962.1 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr15:65681620 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr15:65702610 C>T maps to NM_020962.1 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr15:99459205 C>T maps to NM_000875.3 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr15:99459919 G>A maps to NM_000875.3 K672K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr15:99467846 C>T maps to NM_000875.3 Q906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr15:99459286 G>C maps to NM_000875.3 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:47109290 G>A maps to NM_006546.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr17:47075133 C>T maps to NM_006546.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr17:47103856 T>C maps to NM_006546.3 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr3:185369896 C>T maps to NM_006548.4 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr7:23353158 A>G maps to NM_006547.2 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr7:23509576 G>C maps to NM_006547.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr7:23381742 C>T maps to NM_006547.2 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:160483634 C>G maps to NM_000876.2 P1218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:160477478 C>G maps to NM_000876.2 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr6:160517636 C>T maps to NM_000876.2 T2274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr6:160525707 G>A maps to NM_000876.2 V2356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr6:160468293 A>C maps to NM_000876.2 R719R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:160467652 C>G maps to NM_000876.2 S676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr6:160510168 C>T maps to NM_000876.2 F2117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr6:160468304 G>A maps to NM_000876.2 P722P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr16:1842250 G>A maps to NM_001146006.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr16:1841440 G>A maps to NM_001146006.1 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr17:38609276 C>G maps to NM_001552.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:217543698 C>T maps to NM_000599.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr12:53494635 G>T maps to NM_002178.2 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:46733720 G>A maps to NM_198541.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:46627882 C>T maps to NM_207393.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr19:46627360 C>T maps to NM_207393.1 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:201185732 G>A maps to NM_001164586.1 L3149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:201184745 G>T maps to NM_001164586.1 V3025V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr1:201184691 G>A maps to NM_001164586.1 V3007V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:68703930 C>T maps to NM_002180.2 H661H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr11:68707081 G>A maps to NM_002180.2 G955G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr4:71522980 G>T maps to NM_144646.3 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr22:23917259 G>T maps to NM_020070.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr22:23237768 G>A maps to ENST00000410090 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr22:23237639 G>C maps to ENST00000410090 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:51831952 G>A maps to NM_001101372.1 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr23:130408706 G>A did not map to a codon.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr23:130412725 C>T did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:130411153 G>T did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:130415841 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr23:130411012 G>T did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr23:130419227 T>A did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:130407802 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr23:130409558 G>A did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr23:130409594 C>A did not map to a codon.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr23:130411006 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:130412533 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:130408613 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr23:130419992 C>G did not map to a codon.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr23:130415841 G>T did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:130415193 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr23:130419395 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr3:151161123 G>A maps to NM_178822.4 Q1871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr3:151163991 C>T maps to NM_178822.4 V1259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:151155889 G>A maps to NM_178822.4 I2153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:151166755 G>C maps to NM_178822.4 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:151171334 G>T maps to NM_178822.4 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr3:151161337 C>G maps to NM_178822.4 V1799V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:151154668 G>A maps to NM_178822.4 I2560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr3:151163830 G>C maps to NM_178822.4 S1313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr3:151171208 A>G maps to NM_178822.4 H226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:151155013 G>A maps to NM_178822.4 I2445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:151166223 A>G maps to NM_178822.4 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:118647365 G>A maps to NM_152538.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr3:118647476 G>T maps to NM_152538.2 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr3:118624516 G>C maps to NM_152538.2 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:18661422 G>T maps to NM_032880.4 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:18691762 C>G maps to NM_032880.4 S196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr1:18703307 G>A maps to NM_032880.4 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:18737195 C>A maps to NM_173588.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr11:18731171 G>C maps to NM_173588.3 S920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:117122245 C>T maps to NM_001542.2 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:117150725 C>A maps to NM_001542.2 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:117122161 G>A maps to NM_001542.2 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:117150564 G>T maps to NM_001542.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr1:117120152 G>A maps to NM_001542.2 N1142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr21:41137627 C>G maps to NM_001080444.1 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr21:41142977 C>G maps to NM_001080444.1 S185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:159897152 T>C maps to NM_001135050.1 E1174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr1:159898435 G>A maps to NM_001135050.1 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr1:159912783 G>C maps to NM_001135050.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:159897218 G>A maps to NM_001135050.1 F1152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:159907539 G>A maps to NM_001135050.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:133792551 G>A maps to NM_014987.1 I731I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr11:133791153 C>T maps to NM_014987.1 K822K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr11:133790478 G>A maps to NM_014987.1 F1047F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr11:133796838 G>A maps to NM_014987.1 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:219920153 T>G maps to NM_002181.3 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr2:219920432 G>A maps to NM_002181.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:219920402 C>T maps to NM_002181.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr2:219922389 C>T maps to NM_002181.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr5:140041538 A>T maps to NM_006083.3 K520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:99019905 C>T maps to NM_153687.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr12:99019845 A>G maps to NM_153687.2 N332N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr9:111665222 C>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:111640906 C>G maps to NM_003640.3 L1232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr8:42175233 C>T maps to NM_001556.2 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr8:42183486 G>C did not map to a codon.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr8:42179668 C>G maps to NM_001556.2 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:42179978 G>A maps to NM_001556.2 Q651Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr8:42176859 C>G maps to NM_001556.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr8:42177103 A>G maps to NM_001556.2 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:206649606 G>T maps to NM_014002.3 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:206652435 C>G maps to NM_014002.3 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:206649689 G>A maps to NM_014002.3 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:153780358 C>G did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:153780344 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr7:50450405 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr7:50468249 C>T maps to NM_006060.3 C495C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr7:50468279 C>T maps to NM_006060.3 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:50468168 G>T maps to NM_006060.3 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr7:50450325 G>A maps to NM_006060.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr7:50468300 G>A maps to NM_006060.3 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr7:50467643 C>T maps to NM_006060.3 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr7:50459496 C>T maps to NM_006060.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr2:213872656 C>G maps to ENST00000342002 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr2:213872251 G>A maps to ENST00000342002 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr2:213914559 G>A maps to ENST00000342002 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:213921674 G>C maps to ENST00000342002 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:37947693 G>A maps to NM_012481.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:37947791 G>A maps to NM_012481.3 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr12:56427077 A>T maps to NM_022465.3 K324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:206944332 C>T maps to NM_000572.2 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr11:117859185 G>T maps to NM_001558.3 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr11:117860156 G>A maps to NM_001558.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr11:117866302 G>T did not map to a codon.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr11:117864080 C>T maps to NM_001558.3 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr11:117859157 C>G maps to NM_001558.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr11:117864790 G>A maps to NM_001558.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr11:117864017 C>T maps to NM_001558.3 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr21:34648996 G>A maps to ENST00000433395 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr21:34655450 G>A maps to ENST00000433395 W311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr21:34640811 C>T maps to ENST00000433395 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr5:158745758 C>T maps to NM_002187.2 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr5:158747485 G>C maps to NM_002187.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:18174752 C>T maps to NM_005535.1 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr19:18174782 G>A maps to NM_005535.1 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr19:18172995 C>T maps to NM_005535.1 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr19:18183117 C>T maps to NM_005535.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr19:18180503 G>A maps to NM_005535.1 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr1:67794065 A>C maps to NM_001559.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr1:67833700 G>A maps to NM_001559.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:67795342 G>A maps to NM_001559.2 W246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr5:131993886 G>A maps to NM_002188.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr5:131995943 G>A maps to NM_002188.2 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr23:117892056 C>T did not map to a codon.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr23:117900534 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr23:117900903 A>T did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:114251766 A>G did not map to a codon.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr10:5995117 C>T maps to NM_002189.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr15:81592459 G>A maps to NM_172217.3 Q931Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr15:81585359 C>T maps to NM_172217.3 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr15:81574986 C>T maps to NM_172217.3 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr6:52052417 G>A maps to NM_002190.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr5:148753932 C>G maps to NM_014443.2 *181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:88706323 C>G maps to NM_013278.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr13:21296023 C>A maps to NM_138284.1 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:52103569 G>C maps to NM_052872.3 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr22:17578798 C>T maps to NM_014339.5 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr3:53894239 C>T maps to NM_018725.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:9965626 G>T maps to NM_153461.2 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:9974382 G>A maps to NM_153461.2 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr3:9974313 C>T maps to NM_153461.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr3:9959146 C>T maps to NM_153461.2 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:9974367 C>T maps to NM_153461.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr3:9957396 G>A maps to NM_153483.2 W677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr3:9956435 C>G maps to NM_153483.2 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:9953192 C>G maps to NM_153483.2 S420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:9945785 C>T maps to NM_153483.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:9948762 G>A maps to NM_153483.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr2:103006634 C>T maps to NM_003855.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr2:103013261 G>A maps to NM_003855.2 K514K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr2:103013324 G>A maps to NM_003855.2 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr2:103006642 T>G maps to NM_003855.2 Y359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr2:103053811 G>A maps to NM_003853.2 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:103059777 G>A maps to NM_003853.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr1:207014374 G>A maps to NM_153758.2 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:113532666 G>A maps to NM_000575.3 Q265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr2:113593168 C>A maps to NM_000576.2 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr2:113590326 G>C maps to NM_000576.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:113593148 C>T maps to NM_000576.2 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr2:113591059 G>A maps to NM_000576.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:113831923 G>A maps to NM_032556.4 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:113832423 G>A maps to NM_032556.4 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr2:113832778 C>T maps to NM_032556.4 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr2:113820166 C>T maps to NM_173170.1 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr2:113763615 C>T maps to NM_014440.1 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr2:113765476 G>A maps to NM_014440.1 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr2:113676220 G>A maps to NM_014439.3 W164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:113742421 G>A maps to NM_019618.2 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr2:113742532 C>T maps to NM_019618.2 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:102774204 T>C maps to NM_000877.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr2:102632494 G>A maps to NM_004633.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr3:190366313 G>A maps to NM_002182.3 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr3:190326898 C>T maps to NM_002182.3 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr3:190326924 T>C maps to NM_002182.3 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:29973739 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr23:29935670 T>C did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:29973757 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr23:29959766 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:29972676 G>T did not map to a codon.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr23:29959897 A>T did not map to a codon.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr23:29972742 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr23:29973572 G>C did not map to a codon.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr23:29973249 T>C did not map to a codon.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr23:29417409 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr23:29959895 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:28807508 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr23:104728344 G>T did not map to a codon.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr23:104478537 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr23:105011462 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr23:105011333 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:104984664 T>C did not map to a codon.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr2:102968038 G>A maps to NM_016232.4 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:207039848 C>A maps to NM_018724.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr1:207039229 C>G maps to NM_018724.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:137325793 A>G maps to NM_014432.2 Y276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr6:137329834 C>A maps to NM_014432.2 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr6:137329835 C>A maps to NM_014432.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:136699341 C>T maps to NM_144717.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr3:136701145 G>A maps to NM_144717.3 Q120Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr3:136714355 C>G maps to NM_144717.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:27460068 C>G maps to NM_181079.4 S383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr12:68642643 C>A maps to NM_020525.4 G159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr1:24463708 C>T maps to NM_021258.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr12:56733305 C>T maps to NM_016584.2 Q87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr1:67666417 A>C did not map to a codon.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:67666497 G>A maps to NM_144701.2 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr1:207076385 G>A maps to NM_001185156.1 Q202Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:28515042 C>T maps to NM_145659.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr16:28513302 G>C maps to NM_145659.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr19:14153552 G>T maps to NM_004843.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr19:14142710 C>T maps to NM_004843.2 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr19:14150701 C>T maps to NM_004843.2 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:14143258 G>A maps to NM_004843.2 W54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:14157413 C>T maps to NM_004843.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr19:39760651 G>C maps to NM_172138.1 *201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:39734755 C>T maps to ENST00000392072 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:39734656 G>A maps to ENST00000392072 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr19:39735574 C>T maps to ENST00000392072 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr19:39734537 G>A maps to ENST00000392072 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr1:24484263 G>A maps to NM_170743.2 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:24507309 C>T maps to NM_170743.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr1:24483748 G>A maps to NM_170743.2 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr10:6061421 C>T maps to NM_000417.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr23:70331307 G>C did not map to a codon.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr23:70327695 C>G did not map to a codon.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr23:70327725 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr23:70331383 C>T did not map to a codon.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr23:70329169 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:70330429 T>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:122658408 C>T maps to NM_001014336.1 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr12:122658441 T>C maps to NM_001014336.1 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:55178998 C>T maps to NM_139017.4 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:55206498 C>T maps to NM_139017.4 F547F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr5:55178993 C>T maps to NM_139017.4 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr5:55204150 C>T maps to NM_139017.4 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr16:3119251 C>T maps to ENST00000416912 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr23:1475112 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:1484113 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:1499936 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:1460657 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:1464227 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr23:1475205 C>T did not map to a codon.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr23:1499969 C>A did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr23:1471229 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr23:1484087 A>G did not map to a codon.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr19:50393019 G>A maps to NM_172374.1 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr19:50397530 G>C maps to NM_172374.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:50393763 C>T maps to NM_172374.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:50394271 G>A maps to NM_172374.1 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:50393823 C>A maps to NM_172374.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr19:50398434 G>A maps to NM_172374.1 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr16:27353499 T>G maps to NM_000418.2 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr5:35876083 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:35860996 C>T maps to NM_002185.2 C42C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr5:35860957 C>T maps to NM_002185.2 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr23:155234102 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:155232651 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:155232649 C>T did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr23:155239738 G>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr3:121724235 G>C maps to ENST00000344209 Y78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:166891837 G>A maps to NM_199351.2 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:10793286 G>A maps to NM_017620.2 E485E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr19:10799939 C>T maps to NM_017620.2 G883G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr19:10792774 C>T maps to NM_017620.2 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr2:239079284 G>A maps to NM_030768.2 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr19:15229983 G>T maps to NM_006844.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr19:15234049 C>T maps to NM_006844.3 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr2:86393759 G>C maps to NM_006839.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr2:86406664 C>T maps to NM_006839.2 W67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr2:86373191 C>T maps to NM_006839.2 Q554Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr15:75932209 G>A maps to NM_018285.3 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:131102211 G>A maps to NM_033416.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr17:43922961 G>A maps to NM_175882.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr17:43923858 G>A maps to NM_175882.2 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:43923164 C>G maps to NM_175882.2 S298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:82591398 G>T maps to NM_001144878.1 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr8:82592976 C>A maps to NM_001144878.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr18:12014352 C>T maps to NM_014214.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr18:12028870 A>G maps to NM_014214.1 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr18:22008843 G>C maps to NM_018439.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr7:128038488 C>T maps to NM_000883.3 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr7:128040167 G>A maps to NM_000883.3 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr3:49064435 G>T maps to NM_000884.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr3:49062586 C>T maps to NM_000884.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:49064266 C>T maps to NM_000884.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:49064313 A>G maps to NM_000884.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr6:76728576 T>C did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:76731868 G>A maps to NM_001563.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr3:100976550 G>A maps to NM_016247.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr3:100992517 G>A maps to NM_016247.2 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr3:100962623 G>A maps to NM_016247.2 Q851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:100961750 G>A maps to NM_016247.2 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:101038511 G>A maps to NM_016247.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr10:105048380 G>A maps to NM_032727.3 E485E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr10:105037201 C>T maps to NM_032727.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:62456029 C>A maps to NM_176877.2 L1287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr1:62228586 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:62483542 C>T maps to NM_176877.2 L1295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr1:62545168 C>T maps to NM_176877.2 F1391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:62263048 C>T maps to NM_176877.2 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:62237175 C>T maps to NM_176877.2 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:62263086 A>G maps to NM_176877.2 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr1:62374060 G>A maps to NM_176877.2 L1133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr1:62579820 G>T maps to NM_176877.2 E1520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr17:4893511 C>T maps to NM_001167987.1 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr11:61897937 G>A maps to NM_001040694.1 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr11:61897727 C>T maps to NM_001040694.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:105177450 C>T maps to ENST00000252520 I782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr14:105173275 C>G maps to ENST00000252520 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr14:105174217 C>A maps to ENST00000252520 I538I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr14:105175018 C>G maps to ENST00000252520 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMJ-01A-11D-A42E-08 chr14:105169747 C>T maps to ENST00000252520 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr13:111368179 C>T maps to NM_005537.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr13:111368194 C>T maps to NM_005537.3 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:120610832 G>T maps to NM_019071.2 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:120614877 A>C maps to NM_019071.2 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:6761553 G>C maps to NM_001127582.1 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr2:242644110 G>T maps to NM_032329.4 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr2:220440004 C>T maps to NM_002191.3 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:220437227 C>T maps to NM_002191.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr2:220439959 C>T maps to NM_002191.3 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:41739708 T>C maps to NM_002192.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr7:41739720 C>T maps to NM_002192.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr2:121107200 C>T maps to NM_002193.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr2:121106681 C>T maps to NM_002193.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr2:121106681 C>T maps to NM_002193.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr7:30793521 G>A maps to NM_006774.4 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr7:30795235 C>G maps to NM_006774.4 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr15:41319873 G>A maps to NM_017553.1 Q990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr15:41372083 T>A maps to NM_017553.1 K316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr15:41313218 C>T maps to NM_017553.1 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr15:41289747 G>A maps to NM_017553.1 I1183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr15:41350880 T>C maps to NM_017553.1 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr15:41319808 A>G maps to NM_017553.1 C1011C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr15:41388441 G>A maps to NM_017553.1 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr15:41340452 T>A maps to NM_017553.1 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr18:33077829 C>T maps to NM_001098817.1 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:206921330 C>T maps to NM_017759.4 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr2:206869541 C>T maps to NM_017759.4 V878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr2:206872143 C>T maps to NM_017759.4 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr16:30012077 G>C did not map to a codon.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr2:191231487 C>G maps to NM_002194.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr2:99204040 C>T maps to NM_001134224.1 P968P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:99152286 C>G maps to NM_001134224.1 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr4:143159108 C>T maps to NM_003866.2 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr4:143181646 G>C maps to NM_003866.2 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr4:143044481 C>A maps to NM_003866.2 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr4:143045827 C>G maps to NM_003866.2 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr4:143094901 G>A maps to NM_003866.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr10:134459391 G>A maps to NM_005539.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr10:134563025 C>G maps to NM_005539.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr10:134563303 C>T maps to NM_005539.3 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr1:38332194 T>A maps to ENST00000373026 P854P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr2:234112870 G>A maps to ENST00000359570 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:234079179 G>A maps to ENST00000359570 Q610Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:234106776 C>T maps to ENST00000359570 I910I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr2:234098578 C>T maps to ENST00000359570 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:234072503 C>T maps to ENST00000359570 I464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr2:234079248 C>T maps to ENST00000359570 F633F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:234102590 G>C maps to ENST00000359570 T860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr9:139326390 G>A maps to NM_019892.3 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr9:139325492 C>T maps to NM_019892.3 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T4-01A-11D-A391-08 chr9:139324228 T>C maps to NM_019892.3 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr9:139327495 G>A maps to NM_019892.3 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr10:121541204 A>G maps to NM_014937.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:121586796 G>A maps to NM_014937.2 Q968Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr10:121586894 C>G maps to NM_014937.2 S1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr10:121586872 C>T maps to NM_014937.2 Q994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr10:121586169 C>T maps to NM_014937.2 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr10:121586169 C>T maps to NM_014937.2 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr22:31530065 C>T maps to ENST00000331075 F894F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:1399356 G>A maps to NM_016532.3 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr11:71942079 G>C maps to NM_001567.3 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr11:71939296 G>A maps to NM_001567.3 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr11:71946358 C>G maps to NM_001567.3 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:71949114 C>T maps to NM_001567.3 S1194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr11:71942645 C>T maps to NM_001567.3 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr11:71946370 C>T maps to NM_001567.3 I845I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:71943350 C>T maps to NM_001567.3 H561H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr11:71941436 G>A maps to NM_001567.3 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr11:71948263 C>T maps to NM_001567.3 V992V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr11:15212290 A>G maps to NM_001031853.3 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:15197415 C>A maps to NM_001031853.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr7:155093958 A>C did not map to a codon.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr7:155094080 C>T maps to ENST00000344756 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:155090018 C>T maps to ENST00000344756 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr7:155090348 G>C maps to ENST00000344756 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr7:155100010 G>A maps to ENST00000344756 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr2:118865858 C>G maps to NM_016133.2 Y213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:67263815 T>C maps to NM_005478.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr14:36004657 C>A maps to NM_032594.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr19:7125374 G>T maps to NM_000208.2 V1059V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:7184522 G>A maps to NM_000208.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:7166276 G>C maps to NM_000208.2 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr19:7168031 G>T maps to NM_000208.2 Y519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:7267551 G>C maps to NM_000208.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr19:7152810 G>A maps to NM_000208.2 I719I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr19:7117210 A>G maps to NM_000208.2 C1335C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:7141711 C>G maps to NM_000208.2 V886V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:7142848 G>A maps to NM_000208.2 V840V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:7267623 G>C maps to NM_000208.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:156814377 C>T maps to NM_014215.2 A871A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:156821483 G>A maps to NM_014215.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr1:156815472 C>A maps to NM_014215.2 A704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr1:156821164 G>C maps to NM_014215.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr7:1542570 C>T maps to ENST00000389470 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr7:1538775 G>A maps to ENST00000389470 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr7:1538122 G>C maps to ENST00000389470 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr7:1538784 G>A maps to ENST00000389470 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr7:1539973 G>A maps to ENST00000389470 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:1528999 G>T maps to ENST00000389470 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr8:19682418 C>T maps to NM_018142.2 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr4:106603931 C>T maps to NM_020395.3 Q449Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr4:106603898 G>C maps to NM_020395.3 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:59981822 G>A maps to NM_020748.2 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:59969032 C>T maps to NM_020748.2 Q580Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:59947172 A>T maps to NM_020748.2 V993V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr17:59947180 G>A maps to NM_020748.2 R991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:59999158 G>A maps to NM_020748.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr17:59945028 A>C maps to NM_020748.2 S1168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr1:153737530 G>A maps to ENST00000428986 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr1:153735291 C>T maps to ENST00000428986 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:153723690 C>T maps to ENST00000428986 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:153724859 C>T maps to ENST00000428986 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr1:153719547 T>C did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:153713792 C>A maps to ENST00000428986 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:153701121 G>A maps to ENST00000428986 Q4Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:153735312 C>G maps to ENST00000428986 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr1:153719780 G>A maps to ENST00000428986 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr11:77629998 G>C maps to NM_033547.3 S597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr11:62417401 G>C maps to NM_030628.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr11:62414896 G>A maps to NM_030628.1 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:62416060 G>A maps to NM_030628.1 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr11:62416036 C>T maps to NM_030628.1 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr11:62415619 G>A maps to NM_030628.1 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:62414701 G>C maps to NM_030628.1 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:62415292 G>A maps to NM_030628.1 V753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr11:62415418 C>T maps to NM_030628.1 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:62415211 G>T maps to NM_030628.1 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:212120008 C>T maps to NM_015434.3 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:212180007 T>C maps to NM_015434.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr1:212190364 C>T maps to NM_015434.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:95848844 G>T maps to NM_017864.2 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr8:95848811 G>T maps to NM_017864.2 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr8:95850689 G>C did not map to a codon.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr8:95844221 C>G maps to NM_017864.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:28638403 G>A maps to NM_018250.3 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr9:103055169 T>A maps to NM_014425.2 T877T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr9:103055313 C>T maps to NM_014425.2 R925R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:49770263 C>G maps to NM_153273.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr3:49765534 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:48726173 G>A maps to ENST00000395509 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:48732414 G>A maps to ENST00000443964 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr3:48725747 C>G maps to ENST00000395509 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr3:48732709 G>A maps to ENST00000395509 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr6:33694646 G>C maps to NM_054111.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr6:33694613 G>T maps to NM_054111.4 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr6:154520811 G>T maps to NM_001130700.1 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:154533942 C>T maps to NM_001130700.1 E166E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ZF-AA4V-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:61811325 C>T maps to NM_001134779.1 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr1:44415321 C>T maps to NM_014652.3 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr1:44423126 C>G maps to NM_014652.3 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:44423126 C>T maps to NM_014652.3 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:44422328 G>T maps to NM_014652.3 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr14:24653224 C>G maps to ENST00000458132 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:24656969 G>T maps to ENST00000458132 S104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr14:24651012 G>A maps to ENST00000458132 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr14:24652223 G>A maps to ENST00000458132 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr14:24652247 G>A maps to ENST00000458132 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr14:24653000 G>C maps to ENST00000458132 S658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr13:98667890 A>G maps to NM_002271.4 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr13:98654748 G>A maps to NM_002271.4 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr13:98655285 C>T maps to NM_002271.4 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr13:98660335 G>C maps to NM_002271.4 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr11:9450104 C>T maps to NM_006391.2 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:9424907 G>C maps to NM_006391.2 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr11:9450085 G>A did not map to a codon.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr11:9459518 G>A maps to NM_006391.2 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:9435955 C>T maps to NM_006391.2 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:9450609 G>A maps to NM_006391.2 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr11:9430102 C>G maps to NM_006391.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:30833507 G>A maps to NM_006390.3 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr12:30829449 G>A maps to NM_006390.3 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr12:30802106 G>A maps to NM_006390.3 V744V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:30834720 G>A maps to NM_006390.3 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr12:30792626 G>A maps to NM_006390.3 R771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr1:201844341 C>T maps to NM_018085.4 Q1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:46182625 C>T maps to NM_005897.2 W417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr9:95400336 G>A maps to NM_022755.5 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr2:237405985 G>T maps to ENST00000457693 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:121547357 C>T maps to NM_001023570.2 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:121509012 C>A maps to NM_001023570.2 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:32673402 T>A maps to NM_001160042.1 L454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:32672863 G>A maps to NM_001160042.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr1:32673415 G>A maps to NM_001160042.1 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr7:2613110 G>T maps to NM_152558.3 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr3:51864771 C>A maps to NM_001085479.1 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr15:67649728 G>C maps to NM_001031715.2 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr15:67665745 G>A maps to NM_001031715.2 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr15:67649689 C>T maps to NM_001031715.2 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr3:158980379 C>T maps to NM_001197113.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr3:158983101 C>T maps to NM_001042705.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:158970563 C>G maps to NM_001197113.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr15:90976973 T>C maps to NM_003870.3 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr15:91025470 G>A maps to NM_003870.3 L1171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr15:91021104 C>T maps to NM_003870.3 Q1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr15:90996127 C>G maps to NM_003870.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr15:91025458 G>A maps to NM_003870.3 L1167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr15:91017157 C>T maps to NM_003870.3 R822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr15:91020345 C>T maps to NM_003870.3 N996N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr15:91017819 G>T maps to NM_003870.3 R893R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr15:91017820 G>T maps to NM_003870.3 E894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:75886356 T>G maps to NM_006633.2 Y255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr5:75884787 A>G maps to NM_006633.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr5:75902128 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr5:75979010 G>T maps to NM_006633.2 L1244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr5:75896746 C>T maps to NM_006633.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr1:156498838 C>T maps to NM_178229.4 R1480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:156503867 G>C maps to NM_178229.4 S1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr1:156507073 G>A maps to NM_178229.4 S1107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:156513982 C>T maps to NM_178229.4 R807R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:156521829 C>G maps to NM_178229.4 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:156533447 G>A maps to NM_178229.4 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr3:12949939 C>T maps to ENST00000429247 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr3:12977045 G>A maps to ENST00000429247 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr23:53268443 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr23:53279468 G>C did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:53268458 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr23:53270977 A>T did not map to a codon.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr23:53270973 G>C did not map to a codon.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr23:53279749 T>C did not map to a codon.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr23:53283762 A>G did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:283835 G>A maps to NM_001170738.1 V1062V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:284198 G>C maps to NM_001170738.1 *1183Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr12:247680 G>A maps to NM_001170738.1 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr12:278266 G>A maps to NM_001170738.1 P1020P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr12:266744 C>T maps to NM_001170738.1 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SU-01A-31D-A391-08 chr12:274655 A>G maps to NM_001170738.1 S922S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr12:250442 C>T maps to NM_001170738.1 D715D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr12:247555 C>T maps to NM_001170738.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr12:248354 C>G maps to NM_001170738.1 S609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr7:123152296 G>C maps to NM_178827.4 S33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:123092842 G>C maps to NM_178827.4 S777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr7:123104940 A>G maps to NM_178827.4 F568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr7:123097530 G>C maps to NM_178827.4 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr7:123097452 C>T maps to NM_178827.4 K725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr23:153284895 T>C did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:153284735 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr23:153285223 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr23:153284498 G>C did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr6:79577520 C>T maps to NM_001010844.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr3:10268053 G>T did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr3:10254973 C>G maps to NM_001570.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr12:66638280 G>A maps to NM_007199.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:66597626 C>T maps to NM_007199.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:44180516 A>T maps to NM_016123.3 *461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:78765722 G>A maps to NM_004136.2 K341K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:78782780 G>A maps to NM_004136.2 W698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr15:78758654 G>A maps to NM_004136.2 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr15:78790397 C>T maps to NM_004136.2 S935S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr15:78790482 T>C maps to NM_004136.2 *964Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr4:185329363 C>G maps to NM_002199.3 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:46387391 C>T maps to NM_015649.1 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:46388222 G>A maps to NM_015649.1 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:46387733 C>T maps to NM_015649.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr19:46387754 C>G maps to NM_015649.1 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:46388282 G>A maps to NM_015649.1 H250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr1:234744667 G>C maps to NM_182972.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr19:50163072 G>C maps to NM_001571.5 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:50167972 G>A maps to NM_001571.5 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:397157 C>T maps to NM_002460.3 Y181Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr6:394876 C>G maps to NM_002460.3 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:128587909 C>T maps to NM_001098629.1 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:128582185 G>A maps to NM_001098629.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr7:128588053 C>T maps to NM_001098629.1 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:209968638 G>A maps to NM_006147.2 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:209964140 A>G maps to NM_006147.2 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:209974758 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:209961911 G>A maps to NM_006147.2 V419V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:209964077 G>A maps to NM_006147.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:615237 G>A maps to NM_004031.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr16:85952179 G>A maps to NM_002163.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr14:24633853 C>T maps to NM_006084.4 N227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr19:44222904 G>A maps to NM_019612.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr19:44223732 G>A maps to NM_019612.3 E341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr19:44097128 G>C maps to NM_001007561.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr19:44099433 C>T maps to NM_001007561.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr19:44096789 C>T maps to NM_001007561.2 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:227662878 G>A maps to NM_005544.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:227663124 G>C maps to NM_005544.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:227661378 C>G maps to NM_005544.2 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr2:227659833 A>G maps to NM_005544.2 P1207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr2:227662284 G>A maps to NM_005544.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:227663157 G>A maps to NM_005544.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:227660223 G>A maps to NM_005544.2 L1077L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr13:110435066 C>A maps to NM_003749.2 E1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr13:110435760 G>A maps to NM_003749.2 F880F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr13:110435361 C>T maps to NM_003749.2 P1013P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr23:107978896 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr23:107976877 A>T did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr23:107978992 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr23:107977993 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr23:107977997 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr23:107978049 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr23:107978104 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr23:107978118 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr23:107978139 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr23:107978232 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr23:107978479 C>G did not map to a codon.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr23:107977362 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:107975912 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr23:107977555 C>A did not map to a codon.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr23:107979536 C>T did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:107977170 A>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:107978812 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:107978930 C>G did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:107977713 G>A did not map to a codon.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr23:107977482 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:107979389 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr23:107979219 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr23:107978336 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr23:107978818 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr23:107978023 C>T did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr5:3600760 C>T maps to NM_024337.3 Q451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr5:3600192 C>T maps to NM_024337.3 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr5:3600732 C>T maps to NM_024337.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr5:3599508 C>T maps to NM_024337.3 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr5:3600219 C>G maps to NM_024337.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr5:2749763 G>A maps to NM_033267.4 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr5:2748723 C>T maps to NM_033267.4 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr5:2749161 G>A maps to NM_033267.4 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:54319258 G>A maps to NM_024336.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr16:54319027 A>G maps to NM_024336.2 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr16:54966774 G>A maps to NM_005853.5 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr16:54966651 C>T maps to NM_005853.5 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr16:55360336 C>G maps to NM_024335.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:55363209 G>C maps to NM_024335.2 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:55362777 C>T maps to NM_024335.2 C296C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr14:74961576 G>A maps to NM_194279.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr1:949725 C>T maps to NM_005101.3 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr1:949845 C>T maps to NM_005101.3 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr1:949845 C>T maps to NM_005101.3 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:89182686 C>T maps to NM_002201.4 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr5:50685564 G>C maps to NM_002202.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr5:50683545 C>T maps to NM_002202.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr15:76632860 C>T maps to NM_145805.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr15:74468461 C>T maps to NM_201526.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr15:74426948 T>C maps to NM_001130137.1 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:74427038 T>G maps to NM_001130137.1 R648R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr15:74426444 C>T maps to NM_001130137.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr14:77950715 G>A maps to NM_199296.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr14:77942240 C>T maps to NM_199296.2 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr5:128430719 C>T maps to NM_016048.2 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr19:55964743 G>A maps to NM_024710.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr7:16415850 G>A maps to NM_001101426.3 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr3:128849476 C>G maps to ENST00000418265 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr3:128852988 C>T maps to ENST00000418265 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr19:18546113 C>A maps to NM_016368.4 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:33028023 G>A maps to ENST00000262650 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr20:33030011 G>C did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr20:33059310 C>G maps to ENST00000262650 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr20:33026364 C>G maps to ENST00000262650 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr20:33000424 T>G maps to ENST00000262650 L106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:47347637 A>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr12:2932045 A>G maps to NM_018463.3 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:2933048 C>T maps to NM_018463.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr16:311494 C>T maps to NM_032039.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr16:313302 C>T maps to NM_032039.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr16:312519 C>T maps to NM_032039.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:313398 G>C maps to NM_032039.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:52216259 C>T maps to NM_181501.1 R752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr5:52194073 G>A maps to NM_181501.1 W390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr5:52225453 G>A did not map to a codon.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr1:145534099 C>G maps to NM_003637.3 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:145534180 T>C maps to NM_003637.3 D562D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr1:145536043 T>G maps to NM_003637.3 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:68609617 G>A maps to ENST00000423218 F900F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:68596208 G>T maps to ENST00000423218 I1133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr15:68624686 C>A maps to ENST00000423218 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr15:68649535 C>T maps to ENST00000423218 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:52355783 C>T maps to NM_002203.3 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr5:52351968 C>T maps to NM_002203.3 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr5:52369037 A>G maps to NM_002203.3 G840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr5:52370946 T>G maps to NM_002203.3 S907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr5:52344485 C>G maps to NM_002203.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:42458265 G>A maps to NM_000419.3 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr17:42463197 G>C maps to NM_000419.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:42462406 C>T maps to NM_000419.3 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:48155408 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:48153805 C>T maps to NM_002204.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr17:48155573 G>A maps to NM_002204.2 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr17:48166535 C>T maps to NM_005501.2 I1036I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr2:182395315 T>C maps to NM_000885.4 S868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr2:182359503 C>G maps to NM_000885.4 S435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:182343482 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr2:182392021 A>T did not map to a codon.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr12:54790077 C>G maps to NM_002205.2 *1050S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:54799707 G>T maps to NM_002205.2 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:54799069 G>A maps to NM_002205.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr2:173356196 C>T maps to ENST00000264106 F1017F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr2:173354268 G>A maps to ENST00000264106 Q893Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr12:56088079 G>A maps to ENST00000347027 R842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr12:56091543 A>G maps to ENST00000347027 D492D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr12:56086672 G>A maps to ENST00000347027 S977S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr12:56087053 G>C maps to ENST00000347027 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr10:15760795 C>T maps to NM_003638.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr10:15729951 G>A maps to NM_003638.1 H143H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr10:15600155 G>A maps to NM_003638.1 R895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr10:15760852 G>A maps to NM_003638.1 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:15655711 G>T maps to NM_003638.1 I500I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr10:15634296 G>A maps to NM_003638.1 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr10:15760898 C>G did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr10:15729980 G>A maps to NM_003638.1 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr10:15688845 A>G maps to NM_003638.1 N402N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:37574871 C>T maps to NM_002207.2 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:37818893 G>A maps to NM_002207.2 E851E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr3:37550073 A>C maps to NM_002207.2 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr3:37792017 C>G maps to NM_002207.2 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr16:31425841 C>T maps to ENST00000444228 F705F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr16:31405582 C>T maps to ENST00000444228 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr16:31435475 A>G maps to ENST00000444228 T1087T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr16:31404689 C>T maps to ENST00000444228 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr17:3664706 G>A maps to NM_002208.4 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr17:3661135 G>C maps to NM_002208.4 S295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:3657193 C>T maps to NM_002208.4 K470K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr17:3638125 C>T maps to NM_002208.4 L880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr17:3649147 T>A maps to NM_002208.4 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr16:30510744 G>T maps to NM_002209.2 E694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:30506068 C>T maps to NM_002209.2 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr16:30532937 G>T maps to NM_002209.2 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr16:30506047 C>T maps to NM_002209.2 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr16:30486719 A>G maps to NM_002209.2 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr16:30507527 C>T maps to NM_002209.2 D538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr16:30490650 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr16:30515569 G>A maps to NM_002209.2 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr16:30516708 G>T did not map to a codon.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr16:30492808 C>G maps to NM_002209.2 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr16:31341892 G>A maps to NM_001145808.1 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr16:31308860 C>G maps to NM_001145808.1 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr16:31288341 G>A maps to NM_001145808.1 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr16:31282367 C>G maps to NM_001145808.1 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:31288290 C>G maps to NM_001145808.1 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:31336682 C>T maps to NM_001145808.1 F822F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr16:31288028 G>A maps to NM_001145808.1 E349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:187516804 C>G maps to NM_002210.3 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:187455217 C>T maps to NM_002210.3 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:187500863 T>G maps to NM_002210.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:187533613 T>C maps to NM_002210.3 T853T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr2:187506200 C>T maps to NM_002210.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr2:187455217 C>T maps to NM_002210.3 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr2:187540555 C>T maps to NM_002210.3 Q944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr16:31383089 C>T maps to NM_000887.3 F715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr16:31391115 C>T maps to NM_000887.3 I969I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr16:31371054 G>A maps to NM_000887.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr16:31391654 G>A maps to NM_000887.3 L1043L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:31393134 C>T maps to NM_000887.3 F1133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:33200925 G>A maps to ENST00000374956 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:33224453 C>T maps to ENST00000374956 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr10:33211202 C>T maps to ENST00000374956 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:70523533 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr23:70521662 C>G did not map to a codon.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr23:70522287 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr23:70522297 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:3938611 C>T maps to NM_170678.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr19:3938637 C>T maps to NM_170678.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr21:46323307 G>A maps to NM_000211.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr21:46321535 G>A maps to NM_000211.3 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr21:46321535 G>A maps to NM_000211.3 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr21:46321517 C>T maps to NM_000211.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr21:46309318 C>T maps to NM_000211.3 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr21:46306330 G>A maps to NM_000211.3 F754F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:63920111 G>A maps to ENST00000371092 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:73738801 C>T maps to NM_001005619.1 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:73753569 G>C maps to NM_001005619.1 V1784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:73725399 C>T maps to NM_001005619.1 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr17:73739923 C>A maps to NM_001005619.1 G1031G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr17:73744971 G>A maps to NM_001005619.1 W1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr17:73738529 C>G maps to NM_001005619.1 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:73753634 G>A maps to NM_001005619.1 *1806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr17:73727011 C>G maps to NM_001005619.1 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr17:73727424 C>G maps to NM_001005619.1 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr3:124560235 G>C maps to NM_002213.3 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr3:124592373 G>C maps to NM_002213.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr2:160998507 G>A maps to NM_000888.3 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:161052111 G>A maps to NM_000888.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr12:53586138 G>A maps to NM_000889.1 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr12:53585654 G>C maps to NM_000889.1 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr7:20371497 C>T maps to NM_002214.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr7:20444338 C>T maps to NM_002214.2 H592H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr7:20420306 C>A maps to NM_002214.2 C218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr7:20418896 C>T maps to NM_002214.2 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr7:20444281 A>G maps to NM_002214.2 Q573Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr13:102227802 T>C maps to NM_004791.1 C164C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr13:102220116 C>A maps to NM_004791.1 Y128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr13:102235650 T>A maps to NM_004791.1 C271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr13:102359163 C>G maps to NM_004791.1 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr13:102250647 G>A maps to NM_004791.1 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:52812033 G>T did not map to a codon.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr3:52813597 G>A maps to NM_002215.2 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr3:52823840 G>A maps to NM_002215.2 W764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:52818336 C>G maps to NM_002215.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr10:7774362 G>A maps to NM_002216.2 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr10:7768986 G>A maps to NM_002216.2 Q353Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:52835026 C>T maps to NM_002217.3 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:52836816 G>A maps to NM_002217.3 E568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr3:52836816 G>A maps to NM_002217.3 E568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr3:52851028 G>C maps to ENST00000485816 S786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr3:52859943 G>A maps to ENST00000485816 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr10:7621727 G>A maps to ENST00000256861 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr10:7621947 C>A maps to ENST00000256861 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr10:7683936 C>T maps to ENST00000256861 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr10:7618976 T>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr10:7611658 G>A maps to ENST00000256861 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr23:54777688 G>A did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:54781510 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr23:54783588 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:54777521 C>A did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:54784221 G>A did not map to a codon.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr23:54783665 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr23:54783525 G>T did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:54784820 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:54780384 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr23:54784853 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr23:54784729 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr5:156670653 C>G maps to NM_005546.3 S361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:160854637 G>A maps to NM_017625.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:160854649 G>A maps to NM_017625.2 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr1:160853265 G>A maps to NM_017625.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:160851890 C>T maps to NM_017625.2 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr1:160851087 G>A maps to NM_017625.2 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:160914930 C>G maps to NM_080878.2 *326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:160922431 C>T maps to NM_080878.2 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr23:78616968 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:78616608 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr20:3193861 G>A maps to NM_033453.2 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr15:41794314 C>T maps to NM_002220.1 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr15:41794613 C>A maps to NM_002220.1 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr1:226829729 G>A maps to NM_002221.3 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr1:226827314 C>T maps to NM_002221.3 T832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr19:41223369 G>A maps to NM_025194.2 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr19:41224074 A>T maps to NM_025194.2 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr19:41245404 C>T maps to NM_025194.2 D664D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr3:4716885 G>A maps to ENST00000356617 A907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:4818946 G>A did not map to a codon.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr3:4711445 G>A maps to ENST00000356617 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr3:4699873 C>T maps to ENST00000356617 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr3:4808218 C>T maps to ENST00000356617 S1846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:4856164 G>T maps to ENST00000356617 L2538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr3:4687372 C>A maps to ENST00000356617 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr3:4722271 C>T maps to ENST00000356617 S997S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr12:26640086 G>C maps to NM_002223.2 S1823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr12:26639285 A>G maps to NM_002223.2 D1854D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr12:26812146 G>A maps to NM_002223.2 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr12:26875356 G>A maps to NM_002223.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr12:26818877 G>A maps to NM_002223.2 Q506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:26589262 G>A maps to NM_002223.2 F2220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:26629898 T>C maps to NM_002223.2 R2055R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr12:26749848 C>T maps to NM_002223.2 V1407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr12:26714773 G>C maps to NM_002223.2 S1581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:26553144 G>T maps to NM_002223.2 L2482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:26878698 C>G did not map to a codon.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr12:26647274 T>C did not map to a codon.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr12:26592072 C>T maps to NM_002223.2 Q2210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:26810950 G>A maps to NM_002223.2 Q667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:26640096 C>A maps to NM_002223.2 E1820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:26810990 A>G maps to NM_002223.2 C653C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr12:26634117 C>G maps to NM_002223.2 L2023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:33660623 G>A maps to ENST00000374316 E2526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr6:33636792 G>T maps to ENST00000374316 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:33623612 T>C maps to ENST00000374316 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr6:33636828 G>T maps to ENST00000374316 T695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr6:33654250 C>T maps to ENST00000374316 I1978I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr6:33608293 G>A maps to ENST00000374316 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr6:33638552 G>A maps to ENST00000374316 V849V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr6:33644591 C>T maps to ENST00000374316 I1110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:33657033 C>T maps to ENST00000374316 L2238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr6:33644565 C>T maps to ENST00000374316 Q1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr6:33653565 C>T maps to ENST00000374316 L1877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr10:106075628 G>T maps to NM_033397.2 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:106075002 G>A maps to NM_033397.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:96992596 G>A maps to ENST00000420728 W107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr2:96993456 C>G maps to ENST00000420728 S394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr2:96992693 C>T maps to ENST00000420728 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr2:96992464 G>A maps to ENST00000420728 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr16:19125971 C>A maps to NM_001034841.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr16:19126040 C>G maps to NM_001034841.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr21:35247701 G>A maps to NM_003024.2 L1406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr21:35183343 G>A maps to NM_003024.2 W795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr21:35147079 G>T maps to NM_003024.2 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr21:35239539 T>C maps to NM_003024.2 L1360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr2:24521614 G>A maps to NM_006277.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:24538093 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:24521659 T>C maps to NM_006277.2 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr2:24440777 C>T maps to NM_006277.2 L1268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:24518534 G>A maps to NM_006277.2 Q545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:24518660 G>A maps to NM_006277.2 Q503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr2:24538025 G>C maps to NM_006277.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr2:24522980 G>A maps to NM_006277.2 R381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:24521592 C>A maps to NM_006277.2 E479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr2:24471551 C>T maps to NM_006277.2 Q1078Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr15:40698049 C>T maps to NM_002225.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr1:152882413 G>A maps to NM_005547.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:185269205 G>A maps to NM_006469.4 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:185270113 G>A maps to NM_006469.4 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr2:128263049 T>A maps to NM_017969.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr2:128255776 C>A maps to NM_017969.2 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:128246768 C>G maps to NM_017969.2 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr6:150713490 G>A maps to NM_203395.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr19:49248903 C>T maps to NM_182575.2 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr19:49244221 T>C maps to NM_182575.2 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:49245112 G>A maps to NM_182575.2 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr20:10629301 G>T maps to NM_000214.2 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:10625511 C>T maps to NM_000214.2 Q781Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr20:10620147 A>G maps to NM_000214.2 *1219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr20:10653408 G>A maps to NM_000214.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:10621488 C>T maps to NM_000214.2 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr20:10626117 C>T did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr20:10622200 G>C maps to NM_000214.2 L941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr20:10653477 G>A maps to NM_000214.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr20:10639260 G>T maps to NM_000214.2 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:105618507 G>A maps to NM_002226.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr14:105622233 G>A maps to NM_002226.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:9935059 G>A maps to NM_032492.3 *184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:65316516 G>A maps to NM_002227.2 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:65316593 C>T did not map to a codon.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr1:65335120 G>A maps to NM_002227.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:5126417 T>G maps to NM_004972.3 L1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr9:5126755 C>T maps to NM_004972.3 R1122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr9:5044444 C>T maps to NM_004972.3 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:17953846 C>T maps to NM_000215.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr19:17953148 G>A maps to NM_000215.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr19:17953939 G>A maps to NM_000215.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr19:17954209 G>C maps to NM_000215.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr19:17954683 G>C maps to NM_000215.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:17942578 C>T maps to NM_000215.3 E903E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr19:17950472 C>T did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr19:17945389 G>T maps to NM_000215.3 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr19:17945398 G>C maps to NM_000215.3 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:6107460 G>A maps to NM_001099433.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr4:6087326 C>G maps to NM_001099433.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr4:6107451 C>T maps to NM_001099433.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr4:6066678 C>T maps to NM_001099433.1 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr5:147023723 A>C maps to NM_014790.3 L374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:147015814 G>A maps to NM_014790.3 F549F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr5:147030077 G>A maps to NM_014790.3 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr10:133930750 G>T maps to NM_001105521.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:133918365 C>T maps to NM_001105521.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr10:133930627 C>T maps to NM_001105521.2 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:134014687 G>A maps to NM_032801.3 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr6:15496811 G>A maps to NM_004973.2 K452K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr6:15513613 G>A maps to NM_004973.2 R1137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr6:15410496 C>G maps to NM_004973.2 S75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:139826544 G>C maps to NM_030647.1 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr7:139801780 G>C maps to NM_030647.1 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:59965516 G>A maps to ENST00000356057 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:59965547 C>T maps to ENST00000356057 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr10:64968349 G>A maps to NM_032776.1 Q1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:64952853 G>A maps to NM_032776.1 Q1974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr10:64967166 G>C maps to NM_032776.1 S1421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr10:64975087 G>C maps to NM_032776.1 S317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr10:64974119 A>G maps to NM_032776.1 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr10:64974482 C>A maps to NM_032776.1 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr1:227922991 G>A maps to NM_023007.2 R41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr1:227921240 G>A maps to NM_023007.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:227922980 C>G maps to NM_023007.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:27221636 C>T maps to NM_001145348.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr16:27231897 G>A maps to NM_001145348.1 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:27221611 C>T maps to NM_001145348.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr17:74720007 G>C maps to NM_001081461.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr17:74722446 C>A maps to NM_001081461.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr17:74714846 G>A maps to NM_001081461.1 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr15:42129133 C>T maps to NM_001114632.1 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr5:78610357 T>G maps to NM_152405.4 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr5:78587034 C>G maps to NM_152405.4 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr5:78587100 G>A maps to NM_152405.4 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr5:78610323 C>G maps to NM_152405.4 S770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr5:78596497 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr22:39083954 C>T maps to NM_014876.5 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr8:75227739 C>T maps to NM_020647.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr8:75156997 C>T maps to NM_020647.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr8:75227223 G>T maps to NM_020647.2 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr20:42788427 G>A maps to NM_020433.4 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:87678380 C>T maps to NM_020655.2 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr16:87677960 G>C maps to NM_020655.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:87678050 C>T maps to NM_020655.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr14:24045162 G>A maps to NM_032452.2 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr14:24041061 G>A maps to NM_032452.2 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr14:24044934 G>A maps to NM_032452.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:96125217 G>T maps to NM_003772.3 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:96124928 A>G maps to NM_003772.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr11:96124103 A>T maps to NM_003772.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr19:2252453 C>T maps to NM_144616.3 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr14:23451471 C>A maps to NM_032876.4 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:59248199 C>T maps to NM_002228.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr1:59248505 C>G maps to NM_002228.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:12902734 C>T maps to NM_002229.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr19:12902989 C>T maps to NM_002229.2 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr19:18391385 G>C maps to NM_005354.4 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr17:39919297 G>C maps to NM_021991.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr17:39923801 G>A maps to NM_021991.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:39925390 C>T maps to NM_021991.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr17:39919273 C>T maps to NM_021991.2 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr17:39913895 G>A maps to NM_021991.2 N638N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr17:39914674 G>A maps to NM_021991.2 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr17:39920967 C>T maps to NM_021991.2 K385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr23:8507727 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:8553379 G>A did not map to a codon.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr23:8504982 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr23:8538597 A>G did not map to a codon.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr23:8501088 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:8502367 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:8553349 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr3:124066027 C>A maps to NM_001024660.3 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr3:124436141 G>A maps to NM_001024660.3 L2775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr3:124376604 G>A maps to NM_001024660.3 K1996K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:124165698 G>A maps to NM_001024660.3 L1171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:124211636 G>A maps to NM_001024660.3 V1578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr3:124356150 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:123987852 G>A maps to NM_001024660.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:124398309 G>A maps to NM_001024660.3 T2441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:124210186 G>A maps to NM_001024660.3 V1533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr3:124174040 G>A maps to NM_001024660.3 V1188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:124413236 G>A maps to NM_001024660.3 V2488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr3:124196174 C>T maps to NM_001024660.3 F1393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr3:124418746 G>C maps to NM_001024660.3 S2621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr3:124165104 C>T maps to NM_001024660.3 F1135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:124175548 G>A maps to NM_001024660.3 E1274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr9:730243 C>T maps to NM_015158.2 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr9:713351 C>T maps to NM_015158.2 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr9:713358 C>T maps to NM_015158.2 Q865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr9:734745 A>G did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr9:731233 A>G maps to NM_015158.2 K991K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr9:712748 C>T maps to NM_015158.2 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr9:711200 A>G maps to NM_015158.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:11287303 G>A maps to NM_015493.6 H578H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:11286643 G>A maps to NM_015493.6 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr19:11303663 C>G maps to NM_015493.6 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:11289370 C>A maps to NM_015493.6 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr19:11285368 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:8399277 C>T maps to NM_198471.2 K451K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr1:62740331 G>A maps to NM_181712.4 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:62728782 C>T maps to NM_181712.4 V840V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:62739458 G>A maps to NM_181712.4 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr16:75663369 C>T maps to NM_001130089.1 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr16:75669619 G>T maps to NM_001130089.1 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr16:75663315 G>T maps to NM_001130089.1 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr16:75665678 C>T maps to NM_001130089.1 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr16:75675614 C>T maps to NM_001130089.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr17:40270416 G>A maps to NM_021078.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr3:20136887 C>T maps to NM_003884.4 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr3:20082250 C>T maps to NM_003884.4 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr3:20161114 G>C maps to NM_003884.4 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:20178501 C>T maps to NM_003884.4 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr3:20082250 C>T maps to NM_003884.4 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr3:20167473 C>T maps to NM_003884.4 H497H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr3:20193902 C>T maps to NM_003884.4 V795V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr3:20161147 T>G maps to NM_003884.4 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr6:149954043 C>T maps to NM_007044.2 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr6:149919368 G>A maps to NM_007044.2 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr13:30829723 G>A maps to NM_032116.3 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr13:30782760 C>T maps to NM_032116.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr18:44595907 C>T maps to ENST00000356157 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr18:44589672 C>T maps to ENST00000356157 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr18:44593393 C>T maps to ENST00000356157 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr18:44625667 C>T maps to ENST00000356157 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:57789143 C>T maps to NM_005886.2 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:57789808 G>C maps to NM_005886.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr16:57786830 T>C maps to NM_005886.2 N282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr16:57786698 C>G maps to NM_005886.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr16:57786742 C>G maps to NM_005886.2 S253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:14925612 G>C maps to NM_201628.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:170367163 G>A maps to NM_006063.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:170366330 C>T maps to NM_006063.2 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:170366588 G>T maps to NM_006063.2 G101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr3:127642757 C>A maps to NM_207335.2 S285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr15:65370400 C>T maps to NM_001101362.2 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr7:32909141 G>A maps to NM_015483.2 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr7:32909796 G>A maps to NM_015483.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr11:105925183 T>C did not map to a codon.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr11:105923954 A>G maps to NM_198439.2 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr11:105924563 G>C maps to NM_198439.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:47599017 C>T maps to NM_018095.4 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:42729671 G>A maps to NM_152393.2 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:42732462 G>T maps to NM_152393.2 E574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:42727253 C>T maps to NM_152393.2 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr13:41705449 G>A maps to NM_152903.4 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr13:41706473 A>G maps to NM_152903.4 D58D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:41767322 G>C maps to NM_032138.4 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr13:41766514 G>A maps to NM_032138.4 Q627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr13:41766847 G>A maps to NM_032138.4 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr13:41767784 G>A maps to NM_032138.4 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:67054356 T>C maps to NM_032505.2 N322N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:67049612 C>T maps to NM_032505.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr2:85276690 A>G maps to NM_020122.4 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr12:5021464 C>G maps to NM_000217.2 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:5020927 G>A maps to NM_000217.2 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr12:5020705 C>A maps to NM_000217.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr12:5021485 C>A maps to NM_000217.2 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:5020816 C>T maps to NM_000217.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr12:5020961 G>T maps to NM_000217.2 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr12:5020600 C>T maps to NM_000217.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr1:111061106 G>C maps to NM_005549.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:111060578 G>A maps to NM_005549.2 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr1:111147110 C>T maps to NM_004974.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr1:111146939 G>T maps to NM_004974.2 Y155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:111147038 C>G maps to NM_004974.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr1:111216762 G>C maps to NM_002232.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr1:111216888 G>A maps to NM_002232.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:111216258 C>G maps to NM_002232.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:111216585 C>T maps to NM_002232.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr11:30033502 C>T maps to NM_002233.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:30032767 G>A maps to NM_002233.2 F486F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr11:30032650 C>G maps to NM_002233.2 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr11:30032368 C>T maps to NM_002233.2 K619K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr12:5154245 G>A maps to NM_002234.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr12:5154623 C>T maps to NM_002234.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:4920664 G>T maps to NM_002235.3 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr12:4920040 C>T maps to NM_002235.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr3:156234065 C>T maps to NM_172159.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:156232887 G>T did not map to a codon.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr3:156254481 G>A maps to NM_172159.3 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr3:155838447 G>A maps to NM_172160.2 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:156192556 G>A maps to NM_172159.3 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr1:6158567 C>T maps to NM_003636.3 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr1:6150527 G>A maps to NM_003636.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr20:47991310 G>C maps to NM_004975.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr20:48098448 A>G did not map to a codon.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr20:47991118 C>T maps to NM_004975.2 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr20:48098780 G>A maps to NM_004975.2 D79D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr20:47990815 C>T maps to NM_004975.2 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr20:47990827 C>T maps to NM_004975.2 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr8:73848264 A>G maps to NM_004770.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr8:73480334 A>G maps to NM_004770.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr8:73848438 G>A maps to NM_004770.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr8:73849755 T>C maps to NM_004770.2 N722N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr8:73848918 C>T maps to NM_004770.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr8:73850241 G>A maps to NM_004770.2 K884K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr8:73849398 C>T maps to NM_004770.2 I603I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:17757752 G>A maps to NM_001112741.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr11:17757671 C>T maps to NM_001112741.1 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:75444821 C>G maps to NM_139137.2 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr19:50831718 G>A maps to NM_004977.2 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr19:50826853 G>A maps to NM_004977.2 I452I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr19:50831807 C>A maps to NM_004977.2 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr19:50826727 G>A maps to NM_004977.2 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr1:110768678 G>A maps to NM_004978.4 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:110775578 C>G maps to NM_001039574.2 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr1:110754240 C>T maps to NM_004978.4 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:110766109 C>T maps to NM_004978.4 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr1:110768654 C>T maps to NM_004978.4 L558L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-UY-A9PF-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr23:48826377 C>A did not map to a codon.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr23:48825779 A>G did not map to a codon.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr23:48820024 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr7:119914979 C>T maps to NM_012281.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr7:120381637 T>C maps to NM_012281.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr7:119915121 G>T maps to NM_012281.2 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:112524481 G>C maps to ENST00000315987 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr1:112524688 C>T maps to ENST00000315987 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr1:112525045 C>T maps to ENST00000315987 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr1:112524511 G>A maps to ENST00000315987 N279N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr21:35821725 C>T maps to NM_000219.3 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr2:223918024 C>T maps to NM_080671.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr2:223918015 C>T maps to NM_080671.2 N156N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr2:223917898 C>G maps to NM_080671.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:223917754 C>G maps to NM_080671.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr2:11052944 G>A maps to NM_002236.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr2:11053991 G>A maps to NM_002236.4 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr20:49620848 C>T maps to NM_002237.3 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr18:77623954 G>A maps to NM_012283.1 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr18:77659422 C>T maps to NM_012283.1 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:84270992 C>T maps to NM_172347.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:84256053 G>A maps to NM_172347.2 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr16:84256059 G>A maps to NM_172347.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr16:84256131 T>A maps to NM_172347.2 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr1:210857359 G>A maps to NM_172362.2 R745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr1:211192433 G>A maps to NM_172362.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr1:211276925 C>G maps to NM_172362.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr1:210856623 C>T maps to NM_172362.2 *990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr1:210977473 C>T maps to NM_172362.2 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr1:210857018 C>G maps to NM_172362.2 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr1:211192469 G>A maps to NM_172362.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:211093237 G>A maps to NM_172362.2 D402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:210948796 G>A maps to NM_172362.2 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:211192581 G>C maps to NM_172362.2 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:211192487 G>A maps to NM_172362.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr7:150643985 G>A maps to NM_000238.2 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr7:150644592 G>C maps to NM_000238.2 S992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr7:150654540 G>A maps to NM_000238.2 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:150649797 G>A maps to NM_000238.2 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr7:150648812 G>T maps to NM_000238.2 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr7:150648203 G>T maps to NM_000238.2 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr7:150647493 G>A maps to NM_000238.2 F720F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr7:150647313 G>A maps to NM_000238.2 Y780Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:150654558 G>C maps to NM_000238.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr7:150671862 C>T maps to NM_000238.2 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr7:150671928 C>T maps to NM_000238.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:49934724 C>T maps to NM_012284.1 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:49935416 C>A maps to NM_012284.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:49937725 C>T maps to NM_012284.1 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr12:49935452 G>A maps to NM_012284.1 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr12:49943357 A>T maps to NM_012284.1 K535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr12:49943356 C>T maps to NM_012284.1 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:49944050 C>G maps to NM_012284.1 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr12:49951249 G>A maps to NM_012284.1 S922S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr12:49950152 G>A maps to NM_012284.1 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr17:40321563 C>A maps to NM_012285.2 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:40315335 C>A maps to NM_012285.2 E832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:40323896 G>A maps to NM_012285.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr17:40317637 G>A maps to NM_012285.2 F638F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr17:40321611 G>A maps to NM_012285.2 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr17:40312099 G>A maps to NM_012285.2 L1004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr17:40327650 G>A maps to NM_012285.2 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr14:63483574 G>A maps to NM_139318.3 D57D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr14:63246454 C>G maps to NM_139318.3 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr14:63269242 C>G maps to NM_139318.3 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr14:63174347 G>A maps to NM_139318.3 Q949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr17:61622588 G>A maps to NM_030779.2 G885G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:61615787 C>T maps to NM_030779.2 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr17:61607728 G>A maps to NM_030779.2 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr17:61611623 G>A maps to NM_030779.2 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr17:61615961 C>G maps to NM_030779.2 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr17:61611503 C>T maps to NM_030779.2 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:61601525 C>T maps to NM_030779.2 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr17:61615784 C>T maps to NM_030779.2 F572F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr17:61615775 G>A maps to NM_030779.2 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr17:61607518 C>T maps to NM_030779.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:163360984 G>A maps to NM_033272.2 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:163302587 C>T maps to NM_033272.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:163230024 C>T maps to NM_033272.2 P1093P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr2:163250971 G>T maps to NM_033272.2 S879S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:163374267 G>A maps to NM_033272.2 N288N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr2:163693087 G>C maps to NM_033272.2 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr3:19491661 G>A maps to NM_144633.2 W480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr3:19295254 G>A maps to NM_144633.2 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr3:19479719 C>T maps to NM_144633.2 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr3:19389401 C>A maps to NM_144633.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr3:19575563 G>C maps to NM_144633.2 V1099V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr3:19384100 A>G maps to NM_144633.2 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr3:19295191 C>A maps to NM_144633.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:170159844 G>A maps to NM_001034837.1 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr5:170148846 G>A maps to NM_001034837.1 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:103588902 G>A maps to NM_014591.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:96047360 C>T maps to NM_013434.4 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr2:96048222 C>T maps to NM_013434.4 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr2:96047363 C>T maps to NM_013434.4 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr4:20884249 C>A maps to ENST00000382152 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:128709868 G>A maps to NM_000220.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:160012172 G>C maps to NM_002241.4 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr11:17409116 G>T maps to NM_000525.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr11:17409305 G>A maps to NM_000525.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:17408783 G>A maps to NM_000525.3 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:21319443 C>T maps to NM_021012.4 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr2:233633215 C>T maps to NM_002242.4 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr21:39671487 C>G maps to NM_170736.1 S102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr21:39671930 C>T maps to NM_170736.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:68128890 C>G maps to NM_018658.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr17:68128977 G>A maps to NM_018658.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr17:68128239 C>T maps to NM_018658.1 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr17:68171212 C>T maps to NM_000891.2 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:68171222 G>T maps to NM_000891.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr2:155566290 C>T maps to NM_002239.2 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr2:155555299 C>T maps to NM_002239.2 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr2:155555577 C>T maps to NM_002239.2 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:155711633 C>T maps to NM_002239.2 R439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr2:155555454 G>A maps to NM_002239.2 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr22:38823648 G>A maps to NM_152868.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr22:38823564 C>T maps to NM_152868.1 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr22:38823099 G>A maps to NM_152868.1 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr22:38824092 C>T maps to NM_152868.1 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:128781854 C>T maps to NM_000890.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:128781389 G>C maps to NM_000890.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr21:39086838 G>A maps to NM_002240.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:160054011 C>T maps to NM_004983.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr1:160054062 G>A maps to NM_004983.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:233802575 C>T maps to NM_002245.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr14:88693730 C>T maps to NM_138318.2 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr14:88658716 G>C maps to NM_138318.2 S240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr14:90650737 C>T maps to NM_022054.2 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr14:90651232 C>T maps to NM_022054.2 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr20:43378794 G>A maps to ENST00000372861 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr20:43379085 C>T maps to ENST00000372861 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr6:39284635 C>A maps to NM_032115.3 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr6:39272285 C>A maps to NM_031460.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr10:118957188 G>T maps to NM_181840.1 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:215256744 C>A maps to NM_001017425.2 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:26950988 C>T maps to NM_002246.2 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr2:26950781 C>A maps to NM_002246.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr2:26916024 C>T maps to NM_002246.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr2:26950604 C>T maps to NM_002246.2 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:64067111 A>C maps to ENST00000422670 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:64064955 G>A maps to ENST00000422670 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:64067011 C>G maps to ENST00000422670 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr11:64064471 C>T maps to ENST00000422670 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr11:64064690 C>T maps to ENST00000422670 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr11:64064471 C>T maps to ENST00000422670 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr11:64064639 C>A maps to ENST00000422670 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr19:38817242 C>G maps to NM_004823.1 Y111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr19:38817437 G>A maps to NM_004823.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:65363054 C>A maps to NM_033347.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr11:65361043 G>A maps to NM_033347.1 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr8:140715037 G>A maps to NM_016601.2 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr8:140715045 G>A maps to NM_016601.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr10:78880747 C>T maps to NM_001161352.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr10:78799314 G>A maps to NM_001161352.1 F610F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:78708986 G>C maps to NM_001161352.1 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:78868296 C>A maps to NM_001161352.1 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr10:78799305 C>G maps to NM_001161352.1 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr10:78649234 G>A maps to NM_001161352.1 L1145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr10:78870023 G>C maps to NM_001161352.1 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr3:178968532 G>C maps to NM_171828.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr3:178968690 C>A maps to NM_171828.1 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:70760747 C>T maps to NM_014505.4 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:18104304 G>A maps to ENST00000222249 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr5:113698897 C>T maps to NM_021614.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr5:113698510 G>A maps to NM_021614.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:154705585 G>A maps to NM_002249.4 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:154698405 G>A maps to NM_002249.4 Q563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr1:154698439 C>T maps to NM_002249.4 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr1:154841876 G>T maps to NM_002249.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr1:154794615 G>A maps to NM_002249.4 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr19:44271756 C>A maps to NM_002250.2 E408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr19:44271760 C>T maps to NM_002250.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr19:44284935 G>C maps to NM_002250.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr19:44284956 C>T maps to NM_002250.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr11:2608852 C>A maps to NM_000218.2 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr20:62044921 G>A maps to NM_172107.2 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr20:62038152 G>C maps to NM_172107.2 Y821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr8:133142078 G>A maps to NM_004519.2 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr8:133146598 C>T maps to NM_004519.2 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr8:133141539 G>T maps to NM_004519.2 S863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr1:41284198 G>A maps to NM_004700.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:41283960 C>T maps to NM_004700.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr1:41285617 C>G maps to NM_004700.3 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:41282935 G>C did not map to a codon.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr1:41284237 C>T maps to NM_004700.3 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr6:73843245 C>T maps to NM_001160133.1 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:73843258 G>T maps to NM_001160133.1 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:73787120 C>G maps to NM_001160133.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr6:73332234 C>G maps to NM_001160133.1 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:73751753 G>A maps to NM_001160133.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr6:73905044 C>T maps to NM_001160133.1 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr13:50589919 C>T maps to NM_173605.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr13:50594388 C>T maps to NM_173605.1 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr13:50589875 C>T maps to NM_173605.1 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr20:43727082 G>A maps to NM_002251.3 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr20:43723921 G>A maps to NM_002251.3 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr20:43726794 G>C maps to NM_002251.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr8:99440458 C>T maps to NM_020697.2 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:99440542 G>A maps to NM_020697.2 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr8:99440701 C>A maps to NM_020697.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr8:99440704 C>T maps to NM_020697.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr8:99440965 C>T maps to NM_020697.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:18113261 C>G maps to NM_002252.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:138669287 C>T maps to ENST00000298480 I818I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BT-A42C-01A-11D-A23M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:138662867 G>A maps to ENST00000298480 K645K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:138669335 C>T maps to ENST00000298480 I834I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:138657498 G>A maps to ENST00000298480 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:196342325 A>G maps to NM_198503.2 C449C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr1:196434451 T>A maps to NM_198503.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr1:196436899 A>T maps to NM_198503.2 L159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr1:196250088 G>A maps to NM_198503.2 I937I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr1:196309548 G>A maps to NM_198503.2 Q569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:196227402 G>A maps to NM_198503.2 Y1044Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr1:196300309 T>C maps to NM_198503.2 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr8:36793050 A>T maps to NM_001031836.2 P1021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr8:36662754 T>C maps to NM_001031836.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:36698503 C>G maps to NM_001031836.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr8:36693883 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr8:36642051 C>T maps to NM_001031836.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr8:36644852 G>A maps to NM_001031836.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr8:36766905 G>A maps to NM_001031836.2 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr8:36722033 C>G maps to NM_001031836.2 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr8:36788509 G>T maps to NM_001031836.2 L926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr8:110984712 C>T maps to NM_014379.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr8:110984994 C>G maps to NM_014379.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr8:110980769 G>A maps to NM_014379.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr8:110980337 C>A maps to NM_014379.2 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr8:110984973 C>T maps to NM_014379.2 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr9:2729516 C>T maps to NM_133497.2 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:7256380 G>A maps to NM_001002914.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:7256926 C>G maps to NM_001002914.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:77459557 C>T maps to NM_138444.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr16:29937156 G>C maps to NM_178863.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr16:29918372 C>T maps to NM_178863.2 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr16:29918390 C>T maps to NM_178863.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr11:77728040 C>T maps to NM_023930.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr11:77734250 C>T maps to NM_023930.3 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:34297854 C>T maps to ENST00000422820 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:143586883 G>T maps to NM_020768.3 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr22:37452444 C>T maps to ENST00000403888 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr2:201371691 C>A maps to NM_152387.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr16:67331451 C>T maps to NM_001100915.1 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr16:67324841 G>A maps to NM_001100915.1 I871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:67327462 C>T maps to NM_001100915.1 Q734Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr16:67331520 G>A maps to NM_001100915.1 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr16:67327996 G>C maps to NM_001100915.1 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr16:67331478 G>T maps to NM_001100915.1 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:67327462 C>T maps to NM_001100915.1 Q734Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:73055612 G>A maps to NM_015353.1 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr17:73055694 G>T maps to NM_015353.1 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:36452533 G>A maps to NM_173562.3 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:36437986 C>A maps to NM_173562.3 S38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr1:215793776 G>A maps to NM_016121.3 K755K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr1:215793830 G>T maps to NM_016121.3 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:215775481 G>A maps to NM_016121.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr13:45768090 A>G maps to NM_198404.2 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:58486801 C>T maps to NM_153331.3 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr8:25293947 C>A maps to NM_017634.3 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr13:103450863 G>A maps to NM_024089.2 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr13:103445989 C>T maps to NM_024089.2 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr13:103450975 A>C maps to NM_024089.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:48892914 G>A maps to NM_006801.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr22:38875599 G>A maps to NM_016657.1 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr22:38877347 C>T maps to NM_016657.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr22:38877251 G>A maps to NM_016657.1 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:23382466 C>G maps to NM_001009999.2 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:23395117 C>T maps to NM_001009999.2 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:23408852 C>T maps to NM_001009999.2 A813A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:23376982 G>A maps to NM_001009999.2 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:23397734 G>A maps to NM_001009999.2 E477E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr1:23406143 C>T maps to NM_001009999.2 F718F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr6:18212789 G>A maps to ENST00000388870 K647K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr6:18212780 G>A maps to ENST00000388870 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr6:18218019 C>T maps to ENST00000388870 I764I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr6:18197302 C>T maps to ENST00000388870 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr6:18171673 T>G maps to ENST00000388870 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr11:66888786 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr11:66975110 C>G maps to NM_012308.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:67022405 G>A maps to NM_012308.2 L1123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr11:66888807 G>A maps to NM_012308.2 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr12:121868272 C>T did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:121882021 G>C maps to ENST00000377071 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr12:121882332 C>A maps to ENST00000377071 E704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:121947734 C>A maps to ENST00000377071 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:86707393 C>T maps to NM_001146688.1 A807A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr2:86693696 G>T maps to NM_001146688.1 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:86697423 C>T maps to NM_001146688.1 I539I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr5:137727501 G>A maps to NM_016604.3 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:137771352 C>T maps to NM_016604.3 T1750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr5:137727606 C>T maps to NM_016604.3 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr5:137717270 C>T maps to NM_016604.3 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:137727290 C>G maps to NM_016604.3 S657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr5:137713497 A>G maps to NM_016604.3 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr5:137756482 G>A maps to NM_016604.3 P1268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:44160390 C>T maps to NM_014663.2 F832F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:44128689 T>C maps to NM_014663.2 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr1:44128716 C>G maps to NM_014663.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:44156577 G>A maps to NM_014663.2 Q700Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr1:44169301 C>G maps to NM_014663.2 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr19:5110721 C>T maps to NM_015015.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr19:5138050 C>T maps to NM_015015.2 I840I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr19:5134005 C>T maps to NM_015015.2 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr9:7103806 G>A maps to NM_015061.3 E849E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:7174704 G>A maps to NM_015061.3 Q1049Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:7011858 C>T maps to NM_015061.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr9:6984285 C>T maps to NM_015061.3 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:6893117 C>T maps to NM_015061.3 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:94731430 C>T maps to NM_018039.2 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:94759440 G>C maps to NM_001161630.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr12:431653 C>T maps to NM_001042603.1 R785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr12:420230 C>G did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:475237 G>A maps to NM_001042603.1 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr12:427452 C>A maps to NM_001042603.1 E906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr12:430211 G>C maps to NM_001042603.1 V830V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr12:464389 A>G maps to NM_001042603.1 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr12:416968 G>C maps to NM_001042603.1 S1194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr12:431613 G>A maps to NM_001042603.1 Q799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:202705487 G>C maps to ENST00000367264 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr1:202709879 T>C maps to ENST00000367264 A1038A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:202722142 C>A maps to ENST00000367264 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:202702684 T>A maps to ENST00000367264 A1287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:202703014 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr1:202700984 G>C maps to ENST00000367264 S1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr1:202698959 C>A maps to ENST00000367264 E1494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:53222480 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr23:53223465 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr23:53228047 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:53230842 C>G did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr23:53247477 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr23:53240687 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr24:21867926 A>C did not map to a codon.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr24:21877605 C>T did not map to a codon.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr24:21877818 C>T did not map to a codon.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr24:21877844 C>T did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr24:21878275 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr24:21897325 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr23:44949082 G>T did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr23:44922762 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr23:44922801 C>T did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:44928928 C>T did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:44928991 C>T did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:44929156 C>G did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:44929550 C>G did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:44929588 C>T did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:44922801 C>T did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr23:44918317 G>C did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr23:44941857 C>G did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:44929218 A>G did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr23:44938511 C>T did not map to a codon.
Sequencing variant TCGA-CF-A47W-01A-11D-A23U-08 chr23:44949123 C>T did not map to a codon.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr23:44941857 C>G did not map to a codon.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr23:44969322 G>A did not map to a codon.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr23:44949016 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr23:44922801 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr23:44913156 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr23:44969326 G>T did not map to a codon.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr23:44949017 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr23:44922801 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr23:44894181 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B0-01A-11D-A31L-08 chr23:44921966 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr23:44870229 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr23:44938458 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr23:44920649 C>T did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:44969391 C>A did not map to a codon.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr23:44913135 C>T did not map to a codon.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr23:44922863 C>T did not map to a codon.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr23:44870203 A>T did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr23:44966652 A>T did not map to a codon.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr23:44870203 A>T did not map to a codon.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr23:44948986 G>A did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:44918513 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr23:44949072 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr23:44922669 A>T did not map to a codon.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr23:44870230 G>T did not map to a codon.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr23:44945114 C>T did not map to a codon.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr23:44969425 G>T did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr23:44928965 C>G did not map to a codon.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr23:44919401 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr23:44948994 T>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:44913172 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr23:44870259 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr23:44922801 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr23:44922801 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:44945180 G>T did not map to a codon.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr23:44918598 T>C did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr23:44922801 C>T did not map to a codon.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr23:44966653 G>A did not map to a codon.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr23:44929468 G>A did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr23:44966675 G>A did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr23:44969329 G>T did not map to a codon.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr23:44938404 T>C did not map to a codon.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr23:44922801 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr23:44969326 G>A did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr23:44948996 G>C did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr23:44949082 G>C did not map to a codon.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr23:44942820 T>C did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr23:44938446 G>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:44922694 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr23:44949153 T>C did not map to a codon.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr23:44918258 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr23:44920638 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr23:44942727 T>C did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:44833956 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr23:44922687 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr23:44929016 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr23:44910951 A>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr23:44833959 G>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr23:44948986 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr23:44922801 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr23:44929486 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:44929131 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr23:44948986 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:7751699 C>T maps to NM_001080424.1 I698I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr17:7751552 G>A maps to NM_001080424.1 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr4:55961104 G>A maps to NM_002253.2 F945F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr4:55948762 C>G maps to NM_002253.2 V1234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr4:55961743 C>T maps to NM_002253.2 K939K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:55968636 G>A maps to NM_002253.2 Q676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:55948735 C>T maps to NM_002253.2 P1243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:55962509 C>A did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr4:55948800 G>A maps to NM_002253.2 Q1222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr4:55956122 A>G maps to NM_002253.2 D1064D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr18:61030056 C>T maps to NM_002035.2 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr19:10602914 G>A maps to NM_203500.1 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr19:10597495 T>C did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:10602629 C>T maps to NM_203500.1 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:10602629 C>T maps to NM_203500.1 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:10599871 G>A maps to NM_203500.1 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr19:10602446 C>T maps to NM_203500.1 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:142651350 G>A maps to NM_000420.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr7:142640111 G>C maps to NM_000420.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:91449641 T>C maps to NM_007035.3 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr12:91449291 G>C maps to NM_007035.3 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr6:73951906 G>A maps to ENST00000370385 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:73952216 G>A maps to ENST00000370385 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:62887181 C>A maps to NM_152688.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr6:62757853 T>A maps to NM_152688.2 K89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr6:62611217 G>C maps to NM_152688.2 S181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr8:136561010 G>A maps to NM_006558.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr2:27317760 C>T maps to NM_006488.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr14:24901327 C>T maps to NM_015299.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr14:24906367 C>G maps to NM_015299.2 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr14:24901327 C>G maps to NM_015299.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr14:24901225 C>T maps to NM_015299.2 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr14:24902172 C>T maps to NM_015299.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr1:19549913 G>A maps to NM_015047.1 I784I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr1:19549913 G>A maps to NM_015047.1 I784I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:26951259 G>C maps to NM_014680.2 V1581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:26945943 C>A maps to NM_014680.2 L1896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr17:26969331 T>C maps to NM_014680.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:26967621 C>T maps to NM_014680.2 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:26964033 G>A maps to NM_014680.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:26958553 G>A maps to NM_014680.2 H1414H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr17:26958633 G>A maps to NM_014680.2 Q1388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:26958871 G>T maps to NM_014680.2 V1354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr17:26960991 G>T maps to NM_014680.2 I1061I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr17:26966616 G>C maps to NM_014680.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr17:26945871 C>G maps to NM_014680.2 L1920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr15:64668994 C>T maps to NM_014736.4 E79E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:141314120 G>A maps to NM_014773.3 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr5:141309810 C>T maps to NM_014773.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr5:141309801 C>G maps to NM_014773.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:48641545 C>G maps to NM_001080394.1 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr8:48647882 G>A maps to NM_001080394.1 K873K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr8:48320492 C>T maps to NM_001080394.1 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr16:71949581 G>C maps to NM_014761.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr16:85691123 C>T maps to NM_014615.2 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:85691039 C>A maps to NM_014615.2 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr16:85704673 G>A maps to NM_014615.2 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr16:85687987 C>T maps to NM_014615.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr17:73489626 A>G maps to ENST00000375248 T720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr17:73486836 C>T maps to ENST00000375248 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr17:73491425 C>T maps to ENST00000375248 I936I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr17:73482421 C>G maps to ENST00000375248 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:73489995 C>T maps to ENST00000375248 D808D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr17:73488565 G>C maps to ENST00000375248 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr17:73491111 C>T maps to ENST00000375248 Q915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr17:73485667 C>T maps to ENST00000375248 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr17:73494275 C>T maps to ENST00000375248 L1176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr17:73494287 C>G maps to ENST00000375248 L1180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr8:126061283 G>A maps to ENST00000377985 N786N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr8:126085446 C>G maps to ENST00000377985 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr8:126062838 C>G maps to ENST00000377985 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr3:197430481 C>A maps to NM_014687.1 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:197408131 C>T maps to NM_014687.1 W766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr3:197422852 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr4:6843913 C>T maps to NM_014743.2 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr4:6843852 G>A maps to NM_014743.2 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr4:6865526 C>T maps to NM_014743.2 Q1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr4:6862708 C>G maps to NM_014743.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr6:42832395 G>A did not map to a codon.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr6:42819876 G>A maps to NM_015349.1 K629K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr6:42819891 G>C maps to NM_015349.1 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:105354097 G>A maps to ENST00000453495 R1175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr14:105360911 G>A maps to ENST00000453495 Q1504Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr14:105353089 C>T maps to ENST00000453495 V839V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr14:105354103 G>C maps to ENST00000453495 R1177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr14:105353167 C>T maps to ENST00000453495 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr14:105350342 C>T maps to ENST00000453495 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr14:105353212 G>A maps to ENST00000453495 A880A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr14:105353209 A>G maps to ENST00000453495 P879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr14:105352816 C>T maps to ENST00000453495 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr14:75130425 G>C maps to NM_001039479.1 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr14:75130692 G>A maps to NM_001039479.1 Q760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr14:75131622 C>G maps to NM_001039479.1 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr14:75130443 G>A maps to NM_001039479.1 C817C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr6:24601307 G>A maps to NM_014809.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr6:24596445 C>T maps to NM_014809.3 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:24569157 C>G did not map to a codon.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr1:35919961 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:35940499 C>T maps to NM_024874.4 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:35917361 C>T maps to NM_024874.4 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:35908549 C>T maps to NM_024874.4 E912E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr1:35972683 C>T maps to NM_024874.4 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr19:34791437 C>T maps to NM_014686.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:34818938 G>A maps to NM_014686.3 Q329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:34791500 G>A maps to NM_014686.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr19:34818974 C>G maps to NM_014686.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr9:114151936 G>A maps to NM_001080398.1 Q1294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr9:114176748 G>A maps to NM_001080398.1 I827I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:114148666 G>A maps to NM_001080398.1 R1351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr9:114246639 G>A maps to NM_001080398.1 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr9:114133920 C>A maps to NM_001080398.1 G1751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr20:36634788 G>A maps to NM_014657.1 F771F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr20:36631083 C>T maps to NM_014657.1 V866V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:36625250 G>A maps to NM_014657.1 I966I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr20:36641206 C>A maps to NM_014657.1 G338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr20:36641451 G>C maps to NM_014657.1 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr20:36625163 C>T maps to NM_014657.1 E995E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:4830467 G>C maps to ENST00000450194 L1412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr7:4830401 C>T maps to ENST00000450194 F1390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr18:46385875 G>A maps to NM_001142397.1 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr18:46287780 G>A maps to NM_001142397.1 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr16:15729911 G>A maps to NM_014647.3 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr16:15730084 G>A maps to NM_014647.3 Q87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:15718641 G>A maps to NM_014647.3 Q752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:15715750 G>A maps to NM_014647.3 L826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr16:15705591 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:15718771 G>C maps to NM_014647.3 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:15718958 G>A maps to NM_014647.3 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:43893962 G>A maps to NM_015284.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr1:43895746 C>T maps to NM_015284.2 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:43906166 C>T maps to NM_015284.2 G1519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr1:43916111 C>T maps to NM_015284.2 I2521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr1:43892749 C>G maps to NM_015284.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr1:43916126 C>T maps to NM_015284.2 F2526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr1:43897176 G>T maps to NM_015284.2 E792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:43891313 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:43896195 G>T maps to NM_015284.2 E605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:43892725 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:43894079 C>G maps to NM_015284.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:43898458 C>G maps to NM_015284.2 S965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:43898246 C>T maps to NM_015284.2 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:47181985 G>A maps to NM_014774.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr1:3662657 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:3662531 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:3662768 C>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr16:85100907 C>T maps to NM_014732.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr16:85112026 C>T maps to NM_014732.2 D263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:22627715 G>C maps to ENST00000446597 S671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:22697069 C>T maps to ENST00000446597 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr12:22671061 G>A maps to ENST00000446597 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:22643099 T>G maps to ENST00000446597 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:22659672 C>T maps to ENST00000446597 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr16:27763242 C>A maps to NM_015202.2 R1184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:27640095 G>A maps to NM_015202.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:27751495 C>T maps to NM_015202.2 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr16:27761547 G>A maps to NM_015202.2 V1089V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr16:27720231 G>A maps to NM_015202.2 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr16:27692753 G>A maps to NM_015202.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr16:27788329 C>T maps to NM_015202.2 R1511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr16:27784441 C>T maps to NM_015202.2 L1407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr1:3755527 C>T maps to NM_014704.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:3732013 C>T maps to NM_014704.3 P910P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:3761475 G>A maps to NM_014704.3 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:3731997 T>A maps to NM_014704.3 K916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr1:3732013 C>T maps to NM_014704.3 P910P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr1:3753100 C>T maps to NM_014704.3 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr13:42265514 G>A maps to NM_015058.1 L1269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr13:42524080 G>A maps to NM_015058.1 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr13:42442562 T>C maps to NM_015058.1 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr13:42142407 G>A maps to NM_015058.1 F1881F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr13:42303747 G>A maps to NM_015058.1 V856V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr13:42259310 G>C maps to NM_015058.1 S1400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr14:58949407 C>G maps to ENST00000354386 S1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr14:58934550 C>T maps to ENST00000354386 R838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr14:58954656 T>G maps to ENST00000354386 T1172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr14:58949429 G>A maps to ENST00000354386 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr9:138379115 C>T maps to NM_014811.3 F920F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr9:138376898 C>T maps to NM_014811.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:138377993 G>A maps to NM_014811.3 A546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr9:138377480 C>T maps to NM_014811.3 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr9:138377702 C>A maps to NM_014811.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:46686402 C>G maps to NM_001142673.1 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:2605235 C>G maps to NM_015229.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr17:2601719 G>A maps to NM_015229.3 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr17:2600067 G>A maps to NM_015229.3 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:2604799 C>T maps to NM_015229.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr17:2594937 C>T maps to NM_015229.3 L1237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:2594904 G>A maps to NM_015229.3 L1248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr12:55356880 G>A maps to NM_001098815.1 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr12:55357673 G>T maps to NM_001098815.1 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr12:55356691 G>C maps to NM_001098815.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:6531881 G>T maps to NM_014804.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:6531775 G>A maps to NM_014804.2 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr17:6502619 T>C maps to NM_014804.2 E703E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:39876749 C>T maps to NM_015038.1 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:39878174 G>A maps to NM_015038.1 Q746Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:39876600 C>T maps to NM_015038.1 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:39876716 G>A maps to NM_015038.1 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:39876806 C>T maps to NM_015038.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:39877930 C>A maps to NM_015038.1 S665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr1:39878219 G>C maps to NM_015038.1 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr6:96999336 C>G maps to NM_015323.4 S616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr6:96971030 G>A maps to NM_015323.4 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr18:8824762 G>A maps to ENST00000456698 E1404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr18:8824702 G>A maps to ENST00000456698 V1384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr18:8793079 C>T maps to ENST00000306329 Q679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr18:8784102 G>T maps to ENST00000456698 G691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr18:8825347 G>A maps to ENST00000456698 L1599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr14:55852661 C>A maps to NM_014924.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:55852643 G>A maps to NM_014924.3 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr14:55862700 C>G did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr19:19465234 G>A maps to NM_015329.3 W540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:19459744 C>T maps to NM_015329.3 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:19448016 G>A maps to NM_015329.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr16:67213338 C>A maps to NM_001040715.1 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr1:155886439 G>C maps to NM_014949.2 S510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr1:155903426 C>T maps to NM_014949.2 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr1:155891320 G>A maps to NM_014949.2 Q371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:155891201 C>T maps to NM_014949.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr1:155884094 C>T maps to NM_014949.2 K554K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr1:155891350 G>A maps to NM_014949.2 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr1:155903468 G>A maps to NM_014949.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr10:75557631 A>C maps to NM_015037.2 T1252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr4:154506048 C>T maps to NM_001131007.1 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:154525364 C>T maps to NM_001131007.1 F1067F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:154517429 C>T maps to NM_001131007.1 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr4:154544212 C>T maps to NM_001131007.1 D1341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr4:154517525 C>G maps to NM_001131007.1 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr5:5463635 C>T maps to NM_015325.1 Q1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:5476187 G>C maps to NM_015325.1 L2172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr5:5464729 C>T maps to NM_015325.1 A1761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:5462599 G>A maps to NM_015325.1 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr5:5464639 C>G maps to NM_015325.1 L1731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr5:5460851 C>T maps to NM_015325.1 R469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr5:5457793 G>C maps to NM_015325.1 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr5:5462935 T>C maps to NM_015325.1 T1163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:84862558 G>A maps to NM_014895.2 Q1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr6:84859385 G>C maps to NM_014895.2 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr6:84904791 A>C maps to NM_014895.2 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr18:29522679 G>A maps to NM_014939.3 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr15:79750576 C>T maps to NM_015206.2 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr15:79749967 T>C maps to NM_015206.2 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:105536927 C>T maps to NM_015275.1 D639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr12:105527674 G>T did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr9:34971555 C>T maps to NM_015297.1 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr9:34971522 C>T maps to NM_015297.1 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr9:34977115 G>T maps to NM_015297.1 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr4:123254822 A>G maps to NM_015312.3 S3835S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr4:123122252 C>T maps to NM_015312.3 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr4:123171628 C>T maps to NM_015312.3 T1941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr4:123122273 C>T maps to NM_015312.3 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr4:123249452 G>A maps to NM_015312.3 E3730E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr4:123178470 G>A maps to NM_015312.3 W2147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr4:123170791 G>T maps to NM_015312.3 G1889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr4:123117943 A>C maps to NM_015312.3 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr4:123095790 G>T maps to NM_015312.3 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr4:123145807 T>G maps to NM_015312.3 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr4:123109108 T>C maps to NM_015312.3 D229D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr4:123227106 C>T maps to NM_015312.3 R3250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr4:123151144 C>T maps to NM_015312.3 I1034I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr4:123111187 G>A maps to NM_015312.3 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr4:123255641 C>T maps to NM_015312.3 S3930S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr3:44803049 C>A maps to NM_020696.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr9:34372503 G>A maps to NM_020702.3 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr9:34372104 C>T maps to NM_020702.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr5:175782708 G>A maps to NM_020444.3 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:81199100 G>A maps to NM_018689.1 E503E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:81230242 C>T maps to NM_018689.1 F1110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr15:81213414 C>T maps to NM_018689.1 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr15:81187356 C>G maps to NM_018689.1 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:118223342 A>G did not map to a codon.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr23:118228013 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr23:118220586 A>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:118221777 A>T did not map to a codon.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr23:118223108 A>G did not map to a codon.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr23:118220918 G>C did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:118222275 C>A did not map to a codon.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr23:118223491 G>A did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:118284332 T>C did not map to a codon.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr23:118223066 C>G did not map to a codon.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr23:118250500 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr23:118221634 T>C did not map to a codon.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr23:118223709 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:118222887 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:57179511 G>A maps to NM_020722.1 Q168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:57173840 C>T maps to NM_020722.1 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr4:57164477 C>G maps to NM_020722.1 S28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr10:24669886 G>A maps to NM_019590.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr10:24810778 C>T maps to NM_019590.3 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr10:24809177 G>A maps to NM_019590.3 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr10:24833112 G>C maps to NM_019590.3 V1638V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr10:24669919 T>C maps to NM_019590.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr6:138550949 A>T maps to NM_020340.4 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr6:138566668 C>G maps to NM_020340.4 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:138619774 G>A maps to NM_020340.4 Q1227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:138483237 G>A maps to NM_020340.4 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr6:138559752 G>A maps to NM_020340.4 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr6:138656175 C>T maps to NM_020340.4 Q2065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:138611012 G>A maps to NM_020340.4 L985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr6:138599732 G>A maps to NM_020340.4 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:128696920 C>A maps to NM_020741.2 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr17:44115955 G>C maps to NM_015443.3 S830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr17:44172055 G>C maps to NM_015443.3 S434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr17:44109506 G>C maps to NM_015443.3 S999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:44115974 G>A maps to NM_015443.3 R824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr17:44110826 C>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:44144093 G>A maps to NM_015443.3 Q553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr17:44144913 C>A did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr17:44116391 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr17:44115978 C>T maps to NM_015443.3 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr10:72292375 G>T did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:72300934 C>A maps to NM_014431.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr10:72324121 G>A maps to NM_014431.2 A755A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr10:72298136 G>A maps to NM_014431.2 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr10:72300919 C>T maps to NM_014431.2 F657F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr10:72307084 G>A maps to NM_014431.2 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr10:72324256 C>T maps to NM_014431.2 F800F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr10:70775862 C>G maps to NM_015634.3 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr10:70748746 G>T maps to NM_015634.3 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:97276602 G>C maps to ENST00000421845 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr2:97274329 C>T maps to ENST00000421845 Q552Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr2:97267466 C>T maps to ENST00000421845 P869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:109731741 G>A maps to NM_020775.3 W425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr1:109704541 G>A maps to NM_020775.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr1:109730884 G>A maps to NM_020775.3 K376K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr1:109740253 C>T maps to NM_020775.3 V760V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr7:86569359 G>C maps to NM_001142749.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:86548626 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr7:86521057 G>A maps to NM_001142749.2 L1004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr7:86522362 C>T maps to NM_001142749.2 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr18:34415223 C>G maps to NM_020776.1 S41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr18:34802107 C>G maps to NM_020776.1 S551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:52902153 G>A maps to NM_019600.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr15:52903958 G>A maps to NM_019600.2 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr15:52876943 C>T maps to NM_019600.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr15:52903367 C>T maps to NM_019600.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:101857621 G>T maps to NM_020802.2 E1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr11:101834144 T>A maps to NM_020802.2 A793A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr11:101834474 G>A maps to NM_020802.2 A903A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:113765546 T>C maps to NM_020817.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:113724602 G>A maps to NM_020817.1 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr3:113753923 C>T maps to NM_020817.1 S222S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-K4-A6MB-01A-11D-A31L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr3:113684175 C>T maps to NM_020817.1 W879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr14:93944051 A>G maps to ENST00000393153 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr14:94088399 G>A maps to ENST00000393153 L1629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr14:94155066 C>G maps to ENST00000393153 L2383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:94088397 C>T maps to ENST00000393153 L1629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:94128991 C>T maps to ENST00000393153 Q2251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:94088837 G>A maps to ENST00000393153 S1775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:94109980 C>T maps to ENST00000393153 F2055F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr14:94088426 G>A maps to ENST00000393153 S1638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr14:94156580 C>T maps to ENST00000393153 L2463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr14:94156519 G>A maps to ENST00000393153 L2442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr14:94008942 G>A maps to ENST00000393153 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr14:94089137 C>G maps to ENST00000393153 L1875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr8:95547203 C>T maps to NM_015496.3 W116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:95527161 C>A maps to NM_015496.3 E896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:95538574 C>A maps to NM_015496.3 E633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr8:95508077 G>A maps to NM_015496.3 D1475D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr8:95531372 C>A maps to NM_015496.3 E785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr8:95556076 G>A maps to NM_015496.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr8:95508023 G>A maps to NM_015496.3 L1493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr8:95500997 G>C maps to NM_015496.3 S1792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr8:95504024 G>A maps to NM_015496.3 Q1641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr8:95523457 G>C maps to NM_015496.3 L1115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr8:95556053 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr8:95523739 C>G maps to NM_015496.3 L1021L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr8:95502262 G>A maps to NM_015496.3 Q1730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr4:186112119 T>C maps to NM_020827.1 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr4:186085306 C>T maps to NM_020827.1 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr9:5762587 C>T maps to ENST00000414202 I680I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr9:5774008 C>T maps to ENST00000414202 L1345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr9:5772975 C>T maps to ENST00000414202 I1293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:30317489 C>G maps to NM_020848.2 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr10:30336609 C>T maps to NM_020848.2 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr10:30318524 G>T maps to NM_020848.2 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr10:30316004 A>G maps to NM_020848.2 S1024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr10:30315764 C>T maps to NM_020848.2 R1104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr10:30318172 G>A maps to NM_020848.2 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr10:30317489 C>T maps to NM_020848.2 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr10:30317459 T>C maps to NM_020848.2 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr12:13224173 G>C did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr12:13208677 C>G maps to NM_020853.1 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:13208740 G>A maps to NM_020853.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr18:59941274 T>G maps to NM_020854.3 S941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr18:59855015 C>G maps to NM_020854.3 S93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr18:59954629 G>A maps to NM_020854.3 Q1100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr18:59855230 G>T maps to NM_020854.3 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr18:59854746 G>A maps to NM_020854.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr18:59888693 T>G maps to NM_020854.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr18:59942678 G>A maps to NM_020854.3 V980V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr18:59854863 C>G maps to NM_020854.3 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr2:226446846 C>T maps to NM_020864.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr2:226447596 C>T maps to NM_020864.1 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr2:226446900 C>T maps to NM_020864.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr1:33236373 C>T maps to NM_020888.2 Q532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:33233521 C>T maps to NM_020888.2 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr1:33236197 C>G maps to NM_020888.2 S473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:33238472 G>A maps to NM_020888.2 Q1090Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:33236756 C>T maps to NM_020888.2 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:33237529 C>G maps to NM_020888.2 S917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:33237348 C>T maps to NM_020888.2 Q857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:33237944 C>T maps to NM_020888.2 L1055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:33236669 C>G maps to NM_020888.2 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr3:108295193 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:108272522 C>T maps to NM_020890.2 Q793Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr9:100126407 C>T maps to ENST00000375206 A1315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:100079487 G>T maps to ENST00000375206 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr9:100105770 C>T maps to ENST00000375206 I991I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr9:100087419 G>A maps to ENST00000375206 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr9:100076754 C>T maps to ENST00000375206 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr9:100079438 C>T maps to ENST00000375206 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr4:1377692 C>T maps to NM_020894.2 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr4:1379727 G>A maps to NM_020894.2 Q703Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:7682675 C>G maps to NM_001080429.2 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr19:7682262 C>T maps to NM_001080429.2 R1115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr7:138603283 G>C maps to NM_001164665.1 S363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr7:138602346 A>G maps to NM_001164665.1 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr7:138601914 G>A maps to NM_001164665.1 D819D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr7:138601954 G>C maps to NM_001164665.1 S806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr7:138591728 G>C maps to NM_001164665.1 L1132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr7:138602098 G>T maps to NM_001164665.1 S758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr7:138554444 G>A maps to NM_001164665.1 R1538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr10:118713580 G>C maps to NM_001127211.1 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr16:84520348 G>C maps to NM_020947.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr1:180905027 G>A maps to NM_020950.1 K661K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:180885861 T>A maps to NM_020950.1 L208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:180904938 C>T maps to NM_020950.1 Q632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr1:180885596 C>T maps to NM_020950.1 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr18:43440186 G>A maps to NM_020964.2 G2297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:43497740 G>A maps to NM_020964.2 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:43529493 G>A maps to NM_020964.2 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr18:43523149 C>T maps to NM_020964.2 V640V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr18:43534668 C>G maps to NM_020964.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr18:43496477 G>T maps to NM_020964.2 V1103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr18:43487975 G>A maps to NM_020964.2 L1426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr18:43464724 G>A maps to NM_020964.2 L1721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr22:44692664 G>A maps to NM_001099294.1 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr19:18368616 G>A maps to NM_001145304.1 L1159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr19:18377881 C>T maps to NM_001145304.1 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr4:175231080 G>T maps to NM_001145314.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:176857063 G>C maps to NM_030650.1 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr20:36845696 C>T maps to NM_001029864.1 T953T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr20:36869029 A>T maps to NM_001029864.1 C501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr20:36870148 G>C maps to NM_001029864.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr9:20990270 G>A maps to NM_017794.3 R1718R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr9:20720512 C>T maps to NM_017794.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:20770059 G>A maps to NM_017794.3 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr9:20865953 C>G maps to NM_017794.3 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr9:20820968 C>T maps to NM_017794.3 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr9:20929355 G>A did not map to a codon.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr9:20926298 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr1:233507841 G>A maps to NM_032435.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr2:61315571 C>T maps to NM_001129993.1 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:61315523 G>T maps to NM_001129993.1 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:61308604 C>G maps to NM_001129993.1 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:115421724 A>G maps to NM_133465.2 K509K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr9:115422015 G>C maps to NM_133465.2 R606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr8:22475218 G>A maps to NM_021174.5 K667K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr9:139702036 C>T maps to NM_001039374.4 F500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr9:139701505 G>T maps to NM_001039374.4 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr1:11982701 G>A maps to ENST00000376576 F626F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:113380266 C>A maps to NM_001009899.2 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr3:113376960 C>A maps to NM_001009899.2 E1190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr3:113374151 G>C maps to NM_001009899.2 S2126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:113376933 G>A maps to NM_001009899.2 Q1199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:113375962 C>T maps to NM_001009899.2 Q1522Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr3:113376451 C>T maps to NM_001009899.2 L1359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr23:73962299 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr23:73962898 G>C did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:73963125 C>T did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr23:73963496 C>G did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:73962088 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr23:73964270 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr23:73962681 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr23:73963760 T>C did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr23:73961257 G>C did not map to a codon.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr23:73959939 T>G did not map to a codon.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr23:73963599 A>G did not map to a codon.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr23:73963493 C>A did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr23:73965412 C>G did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:73960547 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:73963136 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:73963863 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr23:73961743 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:73962015 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:6007316 G>A maps to NM_001017969.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:5919701 A>C maps to NM_001017969.2 P2098P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr9:5921267 T>C maps to NM_001017969.2 G1576G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr9:6007546 G>A maps to NM_001017969.2 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr9:5920199 T>C maps to NM_001017969.2 Q1932Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr9:5922488 G>A maps to NM_001017969.2 F1169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr9:6007298 C>T maps to NM_001017969.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr9:5919731 A>T maps to NM_001017969.2 P2088P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr9:6007676 C>T maps to NM_001017969.2 Q37Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr2:8919857 G>A maps to NM_020738.2 I772I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr2:8926338 G>A maps to NM_020738.2 Q646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr2:8871592 C>A maps to NM_020738.2 E1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:8870992 G>A maps to NM_020738.2 Q1725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:8933972 G>A maps to NM_020738.2 Q415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:8926116 G>A maps to NM_020738.2 V661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr2:8943129 G>C maps to NM_020738.2 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr10:94399643 G>T maps to NM_004523.3 E752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr9:116857340 G>A maps to ENST00000259410 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr9:116856477 T>C maps to ENST00000259410 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr9:116854868 G>A maps to ENST00000259410 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr6:17781469 G>A maps to NM_022113.4 L1203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:17804705 G>A maps to NM_022113.4 F780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:17781077 G>A maps to NM_022113.4 V1243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr6:17765155 C>A maps to NM_022113.4 E1535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr6:17834269 G>A maps to NM_022113.4 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:17837138 C>T maps to NM_022113.4 E375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr6:17826043 C>A maps to NM_022113.4 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr8:28974497 G>A maps to NM_015254.3 S1229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:200569536 T>A maps to NM_014875.2 T749T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr1:200572409 C>T maps to NM_014875.2 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr1:200522794 A>T maps to NM_014875.2 V1556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr1:200587689 C>T maps to NM_014875.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:200549456 C>T maps to NM_014875.2 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr1:200586968 G>A maps to NM_014875.2 Q295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:44893818 C>T maps to NM_020242.2 V1364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr3:44872467 G>C maps to NM_020242.2 L1043L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr20:16553908 G>T maps to NM_024704.4 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr20:16486685 C>T maps to NM_024704.4 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr20:16355038 G>A maps to NM_024704.4 I1071I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr20:16359574 G>T maps to NM_024704.4 T1024T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr20:16360473 G>A maps to NM_024704.4 Q725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr20:16492111 G>A maps to NM_024704.4 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr1:21036288 C>T maps to NM_020816.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:21031303 C>T maps to NM_020816.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr1:21024913 C>T maps to NM_020816.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:28045338 G>A maps to NM_031217.3 R855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr11:28098655 C>T maps to NM_031217.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:28098655 C>A maps to NM_031217.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr11:28098655 C>T maps to NM_031217.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:28057954 G>A maps to NM_031217.3 I735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr11:28113033 G>C maps to NM_031217.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr17:43004370 C>T maps to ENST00000438933 K796K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr17:43005491 G>A maps to ENST00000438933 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:72350299 G>C did not map to a codon.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr17:72338022 T>C maps to NM_153209.3 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:241706750 G>C maps to ENST00000373308 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr2:241709123 C>A did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr2:241661250 G>A maps to ENST00000373308 H1580H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr2:241710490 G>C maps to ENST00000373308 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr2:241706708 G>A maps to ENST00000373308 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr2:241706395 C>G maps to ENST00000373308 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr2:241737136 C>T maps to ENST00000373308 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr2:241702641 G>A maps to ENST00000373308 F630F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:10381905 G>A maps to ENST00000377086 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:10342590 G>A maps to ENST00000377086 K478K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr1:10355184 T>A maps to ENST00000377086 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:10335484 G>C did not map to a codon.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr1:10380106 G>T maps to ENST00000377086 E708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr1:10421023 C>T maps to ENST00000377086 L1365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:10292470 C>T maps to ENST00000377086 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr1:10364404 C>A maps to NM_183416.3 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:4904540 C>T maps to NM_006612.5 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:4905848 C>T maps to NM_006612.5 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:4925874 C>G maps to NM_006612.5 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr17:4905367 C>G maps to NM_006612.5 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr5:137519713 G>A maps to NM_005733.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr10:91468952 C>G maps to ENST00000416354 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr10:91479228 C>T maps to ENST00000416354 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr10:91505672 G>A maps to ENST00000416354 Q1381Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr10:91469116 C>T maps to ENST00000416354 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:91498176 C>A maps to ENST00000416354 I1223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:39751994 G>C maps to ENST00000395670 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr12:39716468 C>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:39703447 G>C maps to ENST00000395670 S1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr12:39760202 A>G maps to ENST00000395670 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr12:39751994 G>A maps to ENST00000395670 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr12:39716622 G>C maps to ENST00000395670 S1173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr12:39734070 G>A maps to ENST00000395670 Q736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:200967638 G>A maps to NM_017596.2 I650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr1:200968595 T>C did not map to a codon.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr1:200978080 T>C did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:200954054 C>T maps to NM_017596.2 R1245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:200956032 G>A maps to NM_017596.2 R1210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:200959349 G>A maps to NM_017596.2 I982I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:200954081 G>A maps to NM_017596.2 F1236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:200961508 C>G maps to NM_017596.2 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr1:200972876 G>C maps to NM_017596.2 S350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:200973998 G>A maps to NM_017596.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr1:200971325 G>A maps to NM_017596.2 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr1:200946380 G>A maps to NM_017596.2 Y1415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:200958017 C>T maps to NM_017596.2 L1058L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr1:200954021 G>T maps to NM_017596.2 L1256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr16:29816259 C>A maps to NM_007317.1 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr16:29816196 C>T maps to NM_007317.1 I580I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr15:69714343 A>C maps to NM_138555.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr15:69732771 G>A maps to NM_138555.1 R671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr15:69733150 C>T maps to NM_138555.1 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr9:34257708 G>T maps to NM_194313.2 G632G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:34257246 C>T maps to NM_194313.2 L786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr9:34310979 G>C maps to NM_194313.2 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr9:34257660 C>T maps to NM_194313.2 V648V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:168440762 G>A maps to NM_030615.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr14:104641566 C>T maps to NM_015656.1 F814F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr14:104642733 C>G maps to NM_015656.1 A1203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr1:245850610 G>C maps to NM_018012.3 L1442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:245809540 C>T maps to NM_018012.3 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr1:245582981 G>T maps to NM_018012.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr1:245849191 G>A maps to NM_018012.3 A969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:245771029 C>T maps to NM_018012.3 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:245850472 C>T maps to NM_018012.3 C1396C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:245865905 T>C maps to NM_018012.3 *2109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr9:86495303 G>A maps to NM_017576.1 Q851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:86518141 G>A maps to NM_017576.1 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr9:86465050 G>A maps to NM_017576.1 H1173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr9:86457209 C>T maps to NM_017576.1 K1221K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:51901323 G>A maps to NM_032559.4 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr17:51901944 T>C maps to NM_032559.4 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr17:51901069 C>T maps to NM_032559.4 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr17:51901540 C>T maps to NM_032559.4 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr17:51901911 C>A maps to NM_032559.4 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr17:51900705 G>A maps to NM_032559.4 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr17:51901329 C>T maps to NM_032559.4 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr17:51902193 A>G maps to NM_032559.4 T600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr17:51900568 G>T maps to NM_032559.4 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:45228059 G>A maps to NM_006845.3 Q598Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr1:45213093 C>G maps to NM_006845.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr1:45223596 C>T maps to NM_006845.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr1:45226005 C>T maps to NM_006845.3 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:45221771 G>A maps to NM_006845.3 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr20:30897793 C>T maps to NM_004798.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr20:30898962 G>A maps to NM_004798.3 E461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr20:30919066 C>G maps to NM_004798.3 S730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr20:30897979 C>T maps to NM_004798.3 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr20:30914585 A>C maps to NM_004798.3 I587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr2:26204204 C>T maps to NM_002254.6 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr23:69516994 A>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:69521859 G>A did not map to a codon.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr23:69549358 C>G did not map to a codon.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr23:69626161 C>T did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr23:69594083 G>C did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:69561732 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr5:154395260 G>A maps to NM_001099293.1 K614K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr5:154396082 G>T maps to NM_001099293.1 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr5:154393910 G>T maps to NM_001099293.1 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr5:154396604 C>T maps to NM_001099293.1 G1062G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr12:57975341 C>G maps to NM_004984.2 S967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr10:32311874 C>T maps to NM_004521.2 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr10:32306188 C>A maps to NM_004521.2 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr2:149864526 G>A maps to NM_004522.1 Q832Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:39512363 G>A maps to NM_145027.4 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr6:39328251 C>T maps to NM_145027.4 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr6:39325102 G>C maps to NM_145027.4 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr15:90190164 G>A maps to NM_198525.2 R562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr3:47307253 C>T maps to NM_182902.3 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr3:47278067 C>A maps to NM_182902.3 E656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:170043581 G>A maps to NM_014970.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr1:170004662 C>G maps to NM_014970.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:169952503 G>A maps to NM_014970.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr1:170003618 T>C maps to NM_014970.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr6:33371638 G>A maps to NM_002263.3 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:33374169 C>T maps to NM_002263.3 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr6:33373215 G>C maps to NM_002263.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:145693254 C>G maps to NM_145754.2 S232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr8:145694703 C>T maps to NM_145754.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr8:145697773 C>T maps to NM_145754.2 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr8:145697779 C>G maps to NM_145754.2 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr8:145692626 C>T maps to NM_145754.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr8:145692636 C>T maps to NM_145754.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:7817735 G>A maps to NM_012311.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr10:7816796 G>T maps to NM_012311.2 S222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:55294989 G>A maps to ENST00000291633 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr19:55286722 T>C maps to ENST00000291633 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr19:55286731 G>A maps to ENST00000291633 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:55263167 C>G maps to NM_015868.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr19:55263955 A>C maps to NM_015868.2 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr19:55377273 C>T maps to ENST00000355608 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:158064159 C>A maps to ENST00000368173 R609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr1:158059547 G>C maps to ENST00000368173 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr1:158064738 C>T maps to ENST00000368173 Y717Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:158061273 C>T maps to ENST00000368173 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr1:158059333 C>T maps to ENST00000368173 Q379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:158059371 G>T maps to ENST00000368173 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr1:158061338 A>G maps to ENST00000368173 E504E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:158061330 C>T maps to ENST00000368173 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:36350380 A>T did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:36357213 C>A maps to NM_199180.2 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:36357093 C>T maps to NM_199180.2 V609V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr19:36357114 C>T maps to NM_199180.2 G616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr11:126314946 C>T maps to NM_032531.3 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:126294663 G>T maps to NM_032531.3 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr11:126396466 G>A maps to NM_032531.3 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr11:126343308 C>T maps to NM_032531.3 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr11:126333073 C>T maps to NM_032531.3 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr11:126432807 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:204159860 C>T maps to ENST00000306118 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr4:55564534 A>T maps to NM_000222.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr4:55589837 G>A maps to NM_000222.2 W440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr4:55569978 T>G maps to NM_000222.2 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:55602662 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr12:88912548 A>G maps to NM_000899.4 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:33635144 G>A maps to NM_004795.3 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr13:33635732 C>G maps to NM_004795.3 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr13:33635873 G>A maps to NM_004795.3 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr13:33591258 C>T maps to NM_004795.3 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr4:39448976 G>C maps to NM_175737.3 R877R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:39448202 C>T maps to NM_175737.3 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:39448238 G>A maps to NM_175737.3 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr4:39448277 G>T maps to NM_175737.3 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr4:39448823 C>T maps to NM_175737.3 F826F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr4:39436314 G>A maps to NM_175737.3 K437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr14:104121149 G>A maps to ENST00000445352 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:104121116 C>T maps to ENST00000445352 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr14:104120960 A>G maps to ENST00000445352 T192T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BT-A20T-01A-11D-A14W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:66030505 C>A maps to NM_022822.2 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr11:66029373 C>T maps to NM_022822.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:45853637 G>T maps to NM_177417.2 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr19:45853769 A>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr19:45851298 G>A maps to NM_177417.2 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr6:43029072 G>A maps to NM_201523.1 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr19:12996299 G>A maps to NM_006563.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr8:103662491 C>T maps to NM_005655.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr8:103663468 G>C maps to NM_005655.2 S364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr2:10192501 G>A maps to NM_003597.4 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr2:10187791 C>T maps to NM_003597.4 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr13:74420093 C>T maps to NM_007249.4 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr15:31619855 C>G maps to NM_015995.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:44595285 C>T maps to NM_173484.3 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr4:38682251 C>T maps to NM_016531.5 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr9:110249981 C>T maps to NM_004235.4 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr13:73636552 G>A maps to NM_001730.3 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr13:73649891 C>T maps to NM_001730.3 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr13:73636409 C>T maps to NM_001730.3 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr13:73636357 C>T maps to NM_001730.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr10:3823884 C>T maps to NM_001300.5 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr10:3824276 C>A maps to NM_001300.5 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr10:3824046 C>G maps to NM_001300.5 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr10:3824406 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr10:3824196 C>T maps to NM_001300.5 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:207988723 C>T maps to NM_003709.2 K169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr23:56291622 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr23:56291639 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr9:73002841 C>T maps to NM_001206.2 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr9:73002700 G>A maps to NM_001206.2 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr14:50175882 G>T maps to NM_172193.2 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr7:129756426 G>A maps to NM_014997.3 W132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr14:50238344 C>T maps to NM_014315.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr14:50249292 C>T maps to NM_014315.2 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr14:50244635 C>G maps to NM_014315.2 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:42987035 G>A maps to NM_057161.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:87744969 C>T maps to NM_017566.3 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr16:87782319 G>C maps to NM_017566.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:27933976 C>T maps to NM_020782.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr12:27933985 C>G maps to NM_020782.1 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr12:27933916 C>T maps to NM_020782.1 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:18808296 C>T maps to NM_152375.2 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:18808554 C>T maps to NM_152375.2 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr1:18807545 C>G maps to NM_152375.2 S24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr22:50987788 C>G maps to NM_138433.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr1:205312522 C>T maps to NM_018203.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:205312534 G>C maps to NM_018203.1 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr3:49211747 T>C maps to NM_173546.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr13:70293704 G>T maps to NM_020866.2 S604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr13:70314530 A>G maps to NM_020866.2 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr13:70681398 G>A maps to NM_020866.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr13:70314575 G>A maps to NM_020866.2 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:70413258 C>T maps to NM_020866.2 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr13:70681414 G>A maps to NM_020866.2 H139H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr13:70456575 C>A maps to NM_020866.2 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr13:70681660 G>C maps to NM_020866.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr17:39994309 C>T maps to NM_152467.3 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr17:40004216 G>A maps to NM_152467.3 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:40021194 C>T maps to NM_018143.1 W143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr17:40010620 C>A maps to NM_018143.1 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:40011328 C>A maps to NM_018143.1 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:40011452 C>T maps to NM_018143.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr17:40011357 G>C maps to NM_018143.1 S254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:40010378 A>T maps to NM_018143.1 I580I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr23:117043972 G>C did not map to a codon.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:117032872 A>C did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:117053607 A>G did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr23:117054333 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr23:117043444 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr23:117053580 G>C did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:117033227 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:117043382 G>T did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr18:30350173 C>T maps to NM_020805.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr18:30350104 G>A maps to NM_020805.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr23:24024256 T>C did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr23:24024256 T>C did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr23:24006300 C>T did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr23:24024467 C>G did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr23:24006433 C>G did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr23:24006692 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr1:900516 C>T maps to NM_198317.2 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr1:899320 G>A maps to NM_198317.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:47385223 G>C maps to NM_025010.4 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr1:6653595 G>A maps to NM_014851.2 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr1:6659243 C>T maps to NM_014851.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr1:6653439 G>A maps to NM_014851.2 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr22:20800942 C>T maps to NM_032775.3 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr22:20819314 G>C maps to NM_032775.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr22:20819440 G>A maps to NM_032775.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr22:20819710 G>A maps to NM_032775.3 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:170592591 C>G maps to NM_144711.5 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr2:170592180 C>G maps to NM_144711.5 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr3:183368872 G>C maps to NM_017644.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr3:183388883 C>T maps to NM_017644.3 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr3:183368536 C>T maps to NM_017644.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:183390181 C>A maps to NM_017644.3 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:183396980 T>C maps to NM_017644.3 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr15:86311829 C>T maps to NM_022480.3 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr19:18779478 C>T maps to NM_018316.1 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr19:18778893 G>A maps to NM_018316.1 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr19:18779241 G>A maps to NM_018316.1 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr14:45414369 C>T maps to ENST00000355081 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr6:53519800 G>C maps to NM_001003760.4 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:53516581 C>T maps to NM_001003760.4 W573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:97587082 C>T maps to NM_052904.3 F596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr6:97561858 C>T maps to NM_052904.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr23:21674414 C>A did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr23:21675004 G>A did not map to a codon.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr23:21675186 A>G did not map to a codon.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr23:21675858 G>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr23:21674382 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr11:75139637 G>A maps to NM_001039548.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr11:75139671 C>G did not map to a codon.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr16:84684520 C>T maps to NM_024731.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr16:84690535 C>T maps to NM_024731.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr16:84690922 C>T maps to NM_024731.2 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:84695222 C>T maps to NM_024731.2 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr23:86890750 C>G did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:86877260 T>A did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:86887266 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr23:86868915 C>T did not map to a codon.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr23:86869501 A>G did not map to a codon.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr23:86880668 C>G did not map to a codon.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr23:86773150 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr23:86772964 T>C did not map to a codon.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr23:86773255 T>C did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:39116802 G>A maps to NM_015990.4 W688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr4:39083641 C>T maps to NM_015990.4 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:183209962 G>A maps to NM_130446.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr3:183209738 G>A maps to NM_130446.2 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:183225915 G>A maps to NM_130446.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr7:23183566 C>G maps to NM_001031710.2 S239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr7:23207527 G>T maps to NM_001031710.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr4:88097922 T>G maps to NM_020803.3 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr4:88099701 G>A maps to NM_020803.3 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr4:88104367 C>T maps to NM_020803.3 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr9:21334108 G>A maps to NM_018847.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr9:21333784 A>G maps to NM_018847.2 Y358Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr9:21334287 G>A maps to NM_018847.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr9:21334468 G>A maps to NM_018847.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr9:21334734 G>A maps to NM_018847.2 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr19:51323214 C>T maps to NM_002257.2 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr19:51323488 G>A maps to NM_002257.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr19:51522332 C>T maps to NM_001077500.1 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:51520465 G>A maps to NM_001077500.1 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:51527532 G>T maps to NM_144947.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr19:51537853 G>T maps to NM_019598.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr19:51535177 G>T maps to NM_019598.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:51561863 G>T maps to NM_015596.1 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:51561931 C>A did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:51582811 G>A maps to NM_022046.4 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr19:51329141 G>A maps to NM_017509.2 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:51379979 C>T maps to NM_005551.3 Y153Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:51377989 C>G maps to NM_005551.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:51361377 C>G maps to NM_001648.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:51452190 G>A maps to NM_012427.4 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:51452364 G>A maps to NM_012427.4 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:51452166 A>G maps to NM_012427.4 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr19:51483505 C>T maps to NM_005046.2 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr19:51480875 G>A maps to NM_005046.2 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:51499315 C>T maps to NM_144505.1 *306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:51507040 G>C maps to NM_012315.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr12:10587088 C>T maps to NM_002260.3 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr12:10587971 G>C maps to NM_002260.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:10588537 G>A maps to NM_002260.3 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:9994917 A>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:9147878 G>T maps to NM_005810.3 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr12:9144892 G>A maps to NM_005810.3 W58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr7:139168193 C>T maps to NM_198508.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr12:10532338 G>A maps to NM_007360.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr10:135025325 C>G maps to ENST00000368572 L1402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr10:135011910 C>T maps to ENST00000368572 C659C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:135020849 C>A maps to ENST00000368572 Y1265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr10:135020453 G>C maps to ENST00000368572 L1194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr10:135003171 C>T maps to ENST00000368572 N504N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr10:135032546 C>T maps to ENST00000368572 L1607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr10:135020768 C>T maps to ENST00000368572 N1238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr10:134999800 G>T maps to ENST00000368572 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:186459948 C>T maps to NM_001102416.2 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr12:123067478 G>C maps to NM_014708.4 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr12:123087590 G>A maps to NM_014708.4 L1634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr12:123078908 A>C maps to NM_014708.4 T1444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:123089503 C>G maps to NM_014708.4 L1752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr12:123071246 G>A did not map to a codon.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr12:123102927 G>A maps to NM_014708.4 Q2023Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:123046496 C>T maps to NM_014708.4 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr3:122152512 C>T maps to NM_002264.3 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:122146547 C>T maps to NM_002264.3 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr17:66036858 G>A maps to NM_002266.2 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr13:50299569 G>A maps to NM_002267.3 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr3:160253310 G>A maps to NM_002268.3 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:160245744 G>T maps to NM_002268.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr3:160248718 T>C maps to NM_002268.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:160253345 G>C maps to NM_002268.3 S81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:117013215 A>C did not map to a codon.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr6:117045537 G>A maps to NM_002269.2 Q333Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr6:117023264 G>A maps to NM_002269.2 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:117046957 G>A maps to NM_002269.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr1:32620297 C>G maps to NM_012316.4 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr17:45754465 G>A maps to NM_002265.4 V692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:45748174 G>A maps to NM_002265.4 Q508Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr1:152733512 G>T maps to NM_001025231.1 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:152732541 C>T maps to NM_001025231.1 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr19:47986461 C>T maps to NM_007059.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr19:47984253 G>A maps to NM_007059.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr7:149419540 G>A maps to NM_032534.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr7:149420825 G>A maps to NM_032534.2 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr7:149431122 G>A maps to NM_032534.2 W1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr7:149425659 C>G maps to NM_032534.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr7:149421875 C>G maps to NM_032534.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr17:8273000 T>C maps to NM_213597.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr17:8272482 G>C maps to NM_213597.2 S483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:88327728 C>G maps to NM_016618.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:10670040 G>A maps to NM_023008.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:10671687 C>T maps to NM_023008.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr19:10668239 G>A maps to NM_023008.3 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr19:10668296 G>A maps to NM_023008.3 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:10670160 C>G maps to NM_023008.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:10668502 C>T maps to NM_023008.3 K482K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:10670506 G>A maps to NM_023008.3 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:10675656 C>T maps to NM_023008.3 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:10668317 C>T maps to NM_023008.3 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr7:91842568 G>C maps to NM_194456.1 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr7:91842709 G>C maps to NM_194456.1 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:91851314 T>A maps to NM_194456.1 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr7:91851242 C>G maps to NM_194456.1 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr7:91851265 G>A maps to NM_194456.1 Q505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr7:91844061 G>C maps to NM_194456.1 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:75900672 C>T maps to NM_007043.6 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:75905328 C>A maps to NM_007043.6 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr12:53069126 G>A maps to NM_006121.3 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:38975877 G>T maps to NM_000421.3 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr17:38975914 G>A maps to NM_000421.3 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:38978737 G>A maps to NM_000421.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr17:38975802 G>A maps to NM_000421.3 Q447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:39017932 C>A maps to NM_000223.3 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:39022937 C>T maps to NM_000223.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:39019990 C>T maps to NM_000223.3 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr17:39659034 G>A maps to NM_153490.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr17:39742777 G>T maps to NM_000526.4 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr17:39674668 G>T maps to NM_002275.3 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:39671845 C>T maps to NM_002275.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr17:39767395 C>A maps to NM_005557.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr17:39681483 C>T maps to NM_002276.4 Q154Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr17:39680171 G>A maps to NM_002276.4 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:39681205 G>A maps to NM_002276.4 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr12:53040645 C>G maps to NM_000423.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr12:53044193 G>A maps to NM_000423.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr12:53045824 C>G maps to NM_000423.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr12:53045869 G>A maps to NM_000423.2 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr17:39032711 T>A did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr17:39036070 G>A maps to NM_019010.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr17:39036988 C>T maps to NM_019010.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr17:39041281 C>T maps to NM_019010.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr17:39084820 G>C maps to NM_015515.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:39086302 G>A maps to NM_015515.3 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:39092488 C>A maps to NM_015515.3 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:38859915 G>A maps to NM_019016.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:38857472 C>G maps to NM_019016.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:38856527 G>C maps to NM_019016.2 Y321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:38910243 G>A maps to NM_181534.3 H179H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr17:38922847 C>T maps to NM_181539.4 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:38935996 G>A maps to NM_181537.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr17:38935852 A>G maps to NM_181537.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr17:38953185 C>T maps to NM_181535.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:53186527 A>G maps to ENST00000309505 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr12:53186506 G>A maps to ENST00000309505 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:39551520 G>A maps to ENST00000393998 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr17:39622398 C>T maps to NM_002278.3 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:39538573 C>T maps to NM_021013.3 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr17:39580631 G>A maps to NM_003770.4 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:39580733 G>A maps to NM_003770.4 C14C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr17:39596840 C>T maps to NM_006771.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:39594406 C>T maps to NM_006771.3 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr17:39116696 C>T maps to NM_213656.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr12:53200852 C>T maps to NM_002272.2 *595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr17:39135171 C>T maps to NM_182497.3 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:52913531 G>A maps to NM_000424.3 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr12:52913561 C>T maps to NM_000424.3 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr12:52910467 G>A maps to NM_000424.3 D464D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr12:52910920 C>T maps to NM_000424.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr12:52882203 C>T maps to NM_005554.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:52882122 A>G maps to NM_005554.3 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr12:52882230 C>T maps to NM_005554.3 Q435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:52884915 C>A maps to NM_005554.3 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:52865854 C>T maps to NM_173086.4 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr12:52627196 C>G maps to NM_005556.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr12:52642495 T>G maps to NM_005556.3 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:52938435 G>T maps to NM_033448.2 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr12:52940080 G>A maps to NM_033448.2 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr12:52941682 G>A maps to NM_033448.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:52984644 G>C maps to NM_080747.2 S355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr12:53012080 G>A maps to NM_175068.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr12:53005038 C>A maps to NM_175068.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr12:53012245 G>A maps to NM_175068.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr12:53009993 C>T maps to NM_175068.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr12:53009981 G>A maps to NM_175068.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr12:52962080 G>A maps to NM_175053.3 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:52827959 C>G maps to ENST00000252245 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr12:53165705 G>C maps to NM_015848.4 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr12:53164802 C>A maps to NM_015848.4 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr12:53165943 G>A maps to NM_015848.4 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr12:53162727 G>A maps to NM_015848.4 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr12:53170484 G>A maps to NM_015848.4 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:53164873 G>A maps to NM_015848.4 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr12:53096705 G>A maps to NM_175078.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr12:53088412 G>T maps to NM_175078.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr12:53242450 G>A maps to NM_173352.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr12:53241884 C>T maps to NM_173352.2 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr12:53215787 C>G maps to NM_175834.2 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:53227585 G>A maps to NM_175834.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:53227663 G>C maps to NM_175834.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr12:53227681 C>T maps to NM_175834.2 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr12:53216963 G>C maps to NM_175834.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr12:53292538 C>A maps to NM_002273.3 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr12:53298669 G>A maps to NM_002273.3 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr12:53295805 G>A maps to NM_002273.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:53295783 G>A maps to NM_002273.3 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr12:52567470 C>G maps to NM_182507.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:52565324 G>A maps to NM_001081492.1 Y417Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr12:52574305 G>T maps to NM_182507.2 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr12:52574697 G>A maps to NM_182507.2 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr12:52574707 G>A maps to NM_182507.2 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr12:52680902 C>T maps to NM_002281.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr12:52681091 C>T maps to NM_002281.3 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:52790747 G>A maps to NM_033033.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:52797585 G>A maps to NM_033033.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr12:52714765 G>A maps to NM_002282.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr12:52777486 G>A maps to NM_033045.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:52774310 G>A maps to NM_033045.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:52774947 G>A maps to NM_033045.3 N373N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr12:52758101 G>A maps to NM_002283.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr12:52758858 G>A maps to NM_002283.3 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr12:52695816 C>T maps to NM_002284.3 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr17:39726191 C>A maps to NM_000226.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:39190695 C>T maps to NM_030966.1 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:39183284 C>T maps to NM_031957.1 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr21:45959328 G>A maps to NM_198691.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr21:45959430 G>T maps to NM_198691.2 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr21:46057524 C>G maps to NM_181688.1 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr21:46058038 C>T maps to NM_181688.1 C235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr21:46057648 C>T maps to NM_181688.1 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr21:46117391 G>A maps to NM_198699.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr21:45971218 G>A maps to NM_198693.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr21:45978004 G>C maps to NM_198696.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr21:45994246 C>T maps to NM_198687.1 C204C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr21:45999885 G>T maps to NM_198694.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr21:46021231 C>G maps to ENST00000380102 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr21:46020559 G>A maps to ENST00000380102 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr21:46086428 G>T maps to NM_181684.2 C125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr21:46078006 C>T maps to NM_198697.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr21:46078069 G>A maps to NM_198697.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr21:46074276 G>A maps to NM_198698.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr21:31798110 G>A maps to NM_181622.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr21:31797951 C>G maps to NM_181622.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr21:31812803 G>A maps to NM_181623.1 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr17:39471728 A>T maps to NM_031964.1 C58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr21:31852399 C>T maps to NM_181607.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr21:31859545 G>T maps to NM_181608.1 S41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr21:31869407 A>G maps to ENST00000433652 Y7Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr21:31874369 G>A maps to NM_181611.1 Y13Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr21:31874369 G>A maps to NM_181611.1 Y13Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr21:31874294 G>A maps to NM_181611.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr21:31933599 G>A maps to ENST00000437381 Y3Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr21:31988927 C>G maps to ENST00000399871 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr21:31654986 C>A maps to NM_001085455.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr21:31654539 G>A maps to NM_001085455.1 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr21:31655194 G>C maps to NM_001085455.1 S19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr21:31654595 G>A maps to NM_001085455.1 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr21:31691848 A>G maps to NM_203405.1 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr21:31709533 G>A maps to NM_001077711.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr17:39340938 C>T maps to ENST00000458321 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr17:39340731 G>C maps to ENST00000458321 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:39340932 A>G maps to ENST00000458321 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr17:39341001 G>A maps to ENST00000458321 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr17:39274426 G>A maps to NM_033059.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr17:39324103 A>G maps to NM_033187.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr17:39316559 G>A maps to NM_032524.1 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:39253805 G>A maps to NM_031960.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:39262230 C>A maps to ENST00000377731 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr17:39262014 T>C maps to ENST00000377731 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr11:1606353 G>T maps to NM_001005922.1 C42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr11:1605690 G>T maps to NM_001005922.1 C263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr11:1605846 G>A maps to NM_001005922.1 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr11:1629429 G>T maps to ENST00000359229 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr11:1651189 C>T maps to NM_001001480.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:71238671 C>G maps to NM_001012503.1 S109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr11:71249544 C>T maps to NM_021046.2 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr21:31964949 C>T maps to ENST00000399871 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr21:32185382 G>A maps to NM_175857.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr17:39382933 C>T maps to NM_031961.2 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:39394330 C>T maps to NM_031963.2 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:155145216 G>A maps to NM_173852.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:155142002 G>A maps to NM_173852.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr2:27665506 C>T maps to NM_001168364.1 H30H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:25937224 G>C did not map to a codon.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr12:117909091 C>T maps to ENST00000339824 W872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr12:117914393 C>T maps to ENST00000339824 E819E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr12:117962700 G>A maps to ENST00000339824 F725F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr3:119209462 C>A maps to NM_152305.2 S288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr3:119196158 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:119187926 C>G maps to NM_152305.2 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr1:52498578 C>T maps to NM_138417.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr1:52498479 C>T maps to NM_138417.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr14:56079009 C>T maps to NM_001079521.1 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:56146392 C>A maps to NM_001079521.1 Y1353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr14:56122762 G>A maps to NM_001079521.1 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr14:56142554 G>A maps to NM_001079521.1 L1258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr3:134369697 C>G maps to NM_178554.4 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr3:134323275 C>T maps to NM_178554.4 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:134322837 C>T maps to NM_178554.4 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr2:143746425 C>T maps to NM_001032998.1 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr23:153128263 C>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr23:153128147 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr23:153134150 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr23:153134151 C>A did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr23:153135551 G>T did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:153130410 G>A did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr23:153130846 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr23:153131201 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:153135919 G>A did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr23:153131241 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:153138054 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr23:153133363 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr14:50769706 C>A maps to NM_024884.2 G57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:42164892 C>T maps to NM_032107.4 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr20:42162961 G>A maps to NM_032107.4 E524E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr20:42168833 C>G maps to NM_032107.4 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr20:42165057 C>T maps to NM_032107.4 R689R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr22:41605740 C>T maps to NM_031488.4 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr22:41605776 G>C maps to NM_031488.4 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr22:41616855 C>T maps to NM_031488.4 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr22:41625592 G>A maps to NM_031488.4 K646K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr22:41626225 G>T maps to NM_031488.4 E697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr6:130413971 C>G maps to NM_032438.2 S534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr6:130460876 G>A maps to NM_032438.2 K774K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7N-01A-11D-A391-08 chr18:6238035 G>A maps to NM_173464.3 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr18:6311597 C>T maps to NM_173464.3 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr18:6263972 G>C maps to NM_173464.3 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr18:6046753 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:108676918 A>G maps to NM_145315.3 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr15:63433490 C>A maps to NM_032857.3 Y377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr15:63419768 C>G maps to NM_032857.3 S278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr8:71570031 C>G maps to NM_016027.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr1:201355862 G>C maps to NM_005558.3 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:6882427 C>A maps to NM_002286.5 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr12:6882396 G>A maps to NM_002286.5 W33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:6887432 C>T maps to NM_002286.5 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:6886586 C>G maps to NM_002286.5 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:54868130 G>A maps to NM_002287.3 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr19:55019130 G>A maps to NM_002288.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:48962943 G>C maps to NM_002289.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:48962883 G>A maps to NM_002289.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr18:6997851 C>T maps to NM_005559.2 L1565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr18:7023259 C>T maps to NM_005559.2 G868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr18:7024443 G>C maps to NM_005559.2 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr18:6961982 G>C maps to NM_005559.2 L2471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr18:7044768 G>A maps to NM_005559.2 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr18:6971980 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr18:7010381 G>C maps to NM_005559.2 L1230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr18:7080412 G>A maps to NM_005559.2 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:6955398 T>C maps to NM_005559.2 Q2720Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:7043399 A>G maps to NM_005559.2 C327C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr18:7007211 G>A maps to NM_005559.2 L1396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr18:7038883 G>A maps to NM_005559.2 N496N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr18:6975959 G>C maps to NM_005559.2 L2155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr18:7044768 G>A maps to NM_005559.2 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr18:7043284 G>A maps to NM_005559.2 Q366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr18:6947176 C>T maps to NM_005559.2 E2943E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr18:6966190 G>T maps to NM_005559.2 T2335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr18:7016488 C>A did not map to a codon.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr18:7008608 T>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr6:129794494 G>A maps to NM_000426.3 L2479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr6:129513908 C>T maps to NM_000426.3 Q565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:129796543 A>C maps to NM_000426.3 A2483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr6:129475752 C>T maps to NM_000426.3 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr6:129475824 A>G maps to NM_000426.3 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr6:129486761 C>T maps to NM_000426.3 C416C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr6:129636974 T>C maps to NM_000426.3 S1268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr6:129649558 T>C did not map to a codon.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr6:129601239 G>T maps to NM_000426.3 G829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr6:129785438 C>T maps to NM_000426.3 Q2333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr6:129371192 G>A maps to NM_000426.3 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:129634145 C>T maps to NM_000426.3 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr18:21407358 G>A maps to ENST00000416669 G919G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr18:21492789 C>G maps to ENST00000416669 S2427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr18:21508632 C>T maps to ENST00000416669 F2782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr18:21453130 C>T maps to NM_000227.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr18:21512153 G>A maps to ENST00000416669 L2871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr18:21532954 C>T maps to ENST00000416669 V3248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr18:21485587 G>T maps to ENST00000416669 E2242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr18:21500942 G>A maps to ENST00000416669 V2658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr18:21483085 G>A maps to ENST00000416669 Q2107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr18:21508632 C>T maps to ENST00000416669 F2782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr18:21508200 G>A maps to ENST00000416669 W2766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr18:21399953 C>G maps to ENST00000416669 S768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr18:21453022 G>A maps to NM_000227.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr18:21331012 C>T maps to ENST00000416669 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr6:112462036 C>T maps to NM_001105206.1 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:112506486 C>T maps to NM_001105206.1 E343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr6:112463404 C>G maps to NM_001105206.1 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:112466046 G>A maps to NM_001105206.1 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr6:112575310 C>T maps to NM_001105206.1 W14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr6:112451193 G>A maps to NM_001105206.1 T1339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:112479932 C>A did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr6:112452195 G>A maps to NM_001105206.1 F1314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr6:112437185 G>A maps to NM_001105206.1 F1664F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr20:60906116 G>A maps to NM_005560.3 I1207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr20:60902942 G>C maps to NM_005560.3 L1592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr20:60904246 C>T maps to NM_005560.3 L1394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr20:60912858 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:60893545 G>A maps to NM_005560.3 L2401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:60908289 G>A maps to NM_005560.3 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr20:60900378 G>T maps to NM_005560.3 S1841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr20:60902022 C>T did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr20:60912923 G>A maps to NM_005560.3 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr20:60913288 C>T maps to NM_005560.3 Q585Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr20:60921966 A>C did not map to a codon.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr20:60902719 G>A maps to NM_005560.3 N1601N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr20:60907460 C>T maps to NM_005560.3 V1173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr20:60913629 G>A maps to NM_005560.3 N504N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr20:60907623 G>A maps to NM_005560.3 P1144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:60885532 G>T maps to NM_005560.3 I3514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:60885544 G>T maps to NM_005560.3 V3510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:60886014 G>A maps to NM_005560.3 L3408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr20:60903987 G>A maps to NM_005560.3 F1453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr20:60885765 G>C maps to NM_005560.3 L3467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr20:60921736 C>T did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr7:107594020 G>A maps to NM_002291.2 F1011F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:107599731 C>T maps to NM_002291.2 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr7:107580555 G>A maps to NM_002291.2 I1213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr7:107600929 G>A maps to NM_002291.2 I758I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr7:107592668 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:107571825 G>A maps to NM_002291.2 I1504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr7:107594059 G>C maps to NM_002291.2 L998L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr7:107594153 G>T maps to NM_002291.2 S967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr3:49158973 C>A maps to NM_002292.3 E1718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:49161497 G>A maps to NM_002292.3 Q1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr3:49159499 C>T maps to NM_002292.3 E1600E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr3:49169078 G>C maps to NM_002292.3 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr3:49163836 A>G maps to NM_002292.3 P704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:49169962 C>T maps to NM_002292.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:49166565 G>A maps to NM_002292.3 Q540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:209799288 G>C maps to NM_000228.2 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr1:209799084 C>T maps to NM_000228.2 K628K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:209791918 C>T maps to NM_000228.2 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr1:209806432 G>A maps to NM_000228.2 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr7:107717509 C>T did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr7:107746972 A>C maps to NM_007356.2 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr7:107674700 A>G maps to NM_007356.2 I1590I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr7:107688499 G>A maps to NM_007356.2 L1393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr7:107698334 C>G maps to NM_007356.2 G1107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr7:107703338 C>T maps to NM_007356.2 P1054P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:183094529 A>G did not map to a codon.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr1:183209494 C>T maps to NM_005562.2 L1099L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:183194781 G>A maps to NM_005562.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:183201367 C>G maps to NM_005562.2 S635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr1:183212354 C>T maps to NM_005562.2 I1134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:183201955 G>C maps to NM_005562.2 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr9:133927971 G>C maps to ENST00000355048 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr9:133911630 C>T maps to ENST00000355048 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr9:133945107 C>T maps to ENST00000355048 N980N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr9:133911663 C>T maps to ENST00000355048 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr9:133928004 G>A maps to ENST00000355048 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr9:133960998 G>A maps to ENST00000355048 T1385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr9:133920994 C>T maps to ENST00000355048 C489C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:113976672 C>T maps to NM_005561.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr13:113975983 C>G maps to NM_005561.3 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr13:113974730 G>A maps to NM_005561.3 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr13:113964043 C>T maps to NM_005561.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:119581865 T>C did not map to a codon.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr23:119589269 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr23:119580226 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:182872116 G>A maps to NM_014398.3 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr3:182853667 A>G maps to NM_014398.3 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr2:211301002 G>T maps to NM_001136575.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr2:211306126 C>A maps to NM_001136575.1 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:55499000 G>A maps to NM_018697.3 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr7:55468944 C>T maps to NM_018697.3 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr23:37514950 C>T did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr4:17608492 C>G maps to NM_015907.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:20251206 G>C maps to NM_014713.4 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:20251239 G>A maps to NM_014713.4 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:34046607 G>A maps to NM_133642.3 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr22:33679276 C>T maps to NM_133642.3 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr5:154183238 C>G maps to ENST00000377643 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr4:129127588 G>C maps to NM_018078.2 G772G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr4:129043144 C>T maps to NM_018078.2 D442D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:50829319 C>T maps to ENST00000429001 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr12:50822730 C>G maps to ENST00000429001 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr12:50847394 C>T maps to ENST00000429001 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr12:50831516 G>T did not map to a codon.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr10:930415 G>A maps to NM_015155.1 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr10:875435 C>T maps to NM_015155.1 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr10:871051 A>G maps to NM_015155.1 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr10:866763 C>G maps to NM_015155.1 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr10:860927 G>T maps to NM_015155.1 S593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr10:860753 G>A maps to NM_015155.1 H619H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr10:861004 G>A maps to NM_015155.1 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr15:71125194 A>G maps to NM_018357.2 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr4:113575242 T>C maps to ENST00000509061 Y539Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr5:145524038 C>A maps to NM_020117.9 E551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr5:145512561 G>T maps to NM_020117.9 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:45561758 C>T maps to NM_015340.3 Q755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr3:45500347 A>G maps to NM_015340.3 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr23:64753526 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr23:64753612 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr23:64749123 G>T did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:64734784 T>A did not map to a codon.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr23:64744077 G>T did not map to a codon.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr23:64734802 C>T did not map to a codon.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr23:64751241 C>T did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:37046754 C>T maps to NM_006148.2 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr19:18995035 G>A maps to NM_021267.3 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:19004312 G>C maps to NM_021267.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr15:100996184 G>A maps to ENST00000394113 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr19:8321584 C>G maps to NM_024552.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr12:50528445 G>A maps to NM_147190.2 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr12:50529516 G>A maps to NM_147190.2 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr16:28997738 G>A maps to NM_014387.3 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:28998179 C>T maps to NM_014387.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr16:28997507 C>G maps to NM_014387.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr7:73638408 G>C maps to NM_032464.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:73634088 G>A maps to NM_032464.2 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr6:150004896 G>C maps to NM_004690.2 S443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr6:150005092 G>A maps to NM_004690.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:150001311 C>T maps to NM_004690.2 W764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:150005005 G>A maps to NM_004690.2 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr6:150005690 C>T maps to NM_004690.2 W178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr6:149983113 C>T maps to NM_004690.2 W1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:150023253 C>T maps to NM_004690.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr6:150004839 G>C maps to NM_004690.2 S462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:21553889 G>A maps to NM_014572.2 F904F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:21562106 G>A maps to NM_014572.2 F604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr13:21555654 G>C maps to NM_014572.2 S872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr13:21620024 C>T maps to NM_014572.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr11:111430978 C>T maps to ENST00000375615 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr11:111414780 C>T maps to ENST00000375615 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:36982713 C>G maps to NM_004139.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr20:36997709 C>T maps to NM_004139.2 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:102987461 G>T maps to NM_006562.4 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr2:74725260 G>A maps to NM_001009812.1 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr15:68119287 G>A maps to ENST00000380035 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr15:68118510 G>A maps to ENST00000380035 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr15:68119374 C>T maps to ENST00000380035 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr15:68119374 C>T maps to ENST00000380035 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr21:40794948 A>G maps to NM_152505.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr21:40783686 A>G maps to NM_152505.3 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr21:40800152 C>T maps to NM_152505.3 V89V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KQ-A41Q-01A-11D-A339-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-S5-AA26-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr21:40777912 G>A maps to NM_152505.3 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr16:67974064 G>A maps to NM_000229.1 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:67974010 C>A maps to NM_000229.1 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:152777744 A>T maps to NM_178351.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:152777683 G>A maps to NM_178351.3 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:152770488 G>A maps to NM_178352.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:152770613 G>A maps to NM_178352.2 *115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:152760044 C>T maps to ENST00000417924 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:152749145 C>G maps to NM_178354.2 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr1:152749041 T>G maps to NM_178354.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr1:152659330 G>A maps to NM_014357.4 Q4Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr1:152552262 G>A maps to NM_032563.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr1:152681604 C>T maps to NM_178356.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr1:32745471 C>A maps to ENST00000373562 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr1:32745563 C>T maps to ENST00000373562 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr2:30756160 C>G maps to NM_182551.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:30790972 C>T maps to NM_182551.3 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr16:25189325 G>A maps to ENST00000380963 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr15:43622105 G>C maps to NM_014793.4 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr15:43621511 G>C maps to NM_014793.4 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr15:43621619 C>T maps to NM_014793.4 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr15:43622423 G>C maps to NM_014793.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr9:139847414 C>T maps to NM_178536.3 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr9:139658198 C>G maps to NM_203347.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr9:130911942 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:130914209 C>T maps to ENST00000373013 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr9:138557166 G>A maps to ENST00000277526 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr9:138556078 G>A maps to ENST00000277526 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr9:138557737 G>A maps to ENST00000277526 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr10:98715432 G>A maps to NM_001170765.1 E352E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr10:98715439 G>T maps to NM_001170765.1 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr13:46728948 G>A maps to NM_002298.4 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr13:46718647 C>T maps to NM_002298.4 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr13:46708312 C>T maps to NM_002298.4 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr5:169701310 C>T maps to NM_005565.3 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr2:136587247 T>C did not map to a codon.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr2:136575147 C>T maps to NM_002299.2 E490E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr2:136562345 G>T maps to NM_002299.2 I1485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr2:136594448 G>A maps to NM_002299.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr2:136570088 A>G maps to NM_002299.2 H715H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr2:136548243 G>A maps to NM_002299.2 I1773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMJ-01A-11D-A42E-08 chr2:136567429 C>T maps to NM_002299.2 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr15:66845510 G>T maps to NM_207338.2 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr15:66842424 G>A maps to NM_207338.2 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr15:66840869 G>A maps to NM_207338.2 I554I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr10:103868830 C>T maps to NM_001113407.1 K320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr10:103869735 C>T maps to NM_001113407.1 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr4:16900018 G>A maps to NM_001290.3 Y30Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr4:16510156 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr4:16760786 G>A maps to NM_001290.3 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr4:16504432 G>A maps to NM_001290.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr10:88441525 C>T maps to NM_001171610.1 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr10:88439910 G>A maps to NM_001171610.1 Q106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr15:59499498 C>T maps to NM_033195.1 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr15:59499918 G>A maps to NM_033195.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr11:18460093 G>C maps to NM_017448.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:18434293 G>A maps to NM_017448.3 E10E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr16:75149486 C>T maps to NM_153486.3 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr16:75146304 G>C maps to NM_153486.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:75146304 G>C maps to NM_153486.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr19:11213401 C>T maps to NM_000527.4 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr19:11215959 C>T maps to NM_000527.4 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr19:11217344 G>T maps to NM_000527.4 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:11227635 A>T maps to NM_000527.4 K603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:11227585 C>G maps to NM_000527.4 S586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:54474747 G>A maps to NM_001010978.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr1:22142463 G>A maps to NM_001013693.2 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:22141308 C>T maps to NM_001013693.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:36248960 G>T maps to NM_174902.2 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr11:36250844 G>C maps to NM_174902.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr11:36250736 G>A maps to NM_174902.2 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr11:36248839 G>A maps to NM_174902.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr11:36248707 C>T maps to NM_174902.2 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:25893368 C>T maps to NM_015627.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:25880455 G>A maps to NM_015627.2 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr23:140271003 A>C did not map to a codon.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr23:140271100 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr23:140271182 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:140271167 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr22:44892893 G>C maps to NM_032287.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr22:44892717 T>A maps to NM_032287.2 *240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr13:53313189 G>A maps to NM_007015.2 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr4:109004528 G>A maps to NM_016269.4 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:226127071 G>C maps to NM_003240.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr1:226125380 G>T maps to NM_003240.3 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr1:226127679 C>T maps to NM_003240.3 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr3:156746101 A>T maps to NM_001004316.2 K527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:33752201 G>A maps to NM_181336.3 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:65640103 G>A maps to NM_014319.4 *912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr12:65634706 C>G maps to NM_014319.4 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:65640031 C>G maps to NM_014319.4 S888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:54662153 G>A maps to NM_024316.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr19:54971985 C>T maps to NM_052925.2 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:54963383 G>A maps to ENST00000431846 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr19:54963335 G>A maps to ENST00000431846 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr19:54965838 A>G maps to ENST00000431846 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:54973371 G>A maps to NM_198988.1 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:54973626 C>T maps to NM_198988.1 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr15:52246700 C>G maps to NM_138792.2 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr15:52257977 G>T maps to NM_138792.2 S261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr7:127894788 G>A maps to NM_000230.2 W159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr1:66083653 C>T maps to NM_002303.5 I740I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:66102577 T>C maps to NM_002303.5 N1126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:66081709 C>G maps to NM_002303.5 S672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:43232528 G>C maps to NM_022356.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:43213044 G>A maps to NM_022356.3 F651F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr1:43228146 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:43232624 C>T maps to NM_022356.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr1:43223455 C>A maps to NM_022356.3 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:43224968 C>G maps to NM_022356.3 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr3:189704648 C>G maps to NM_018192.3 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:189706729 C>T maps to NM_018192.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr3:189705369 G>A maps to NM_018192.3 Y348Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr3:189675727 C>T maps to NM_018192.3 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr1:65895676 T>A maps to NM_017526.4 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr4:1843343 C>T maps to NM_012318.2 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr4:1843115 G>C maps to NM_012318.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr4:1836637 C>T maps to NM_012318.2 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr8:38261978 G>C maps to ENST00000379957 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:51450270 C>T maps to ENST00000448283 Q314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr12:51450185 G>A maps to ENST00000448283 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr12:51442968 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr12:51449970 G>C maps to ENST00000448283 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr12:51450284 G>T maps to ENST00000448283 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr7:2565140 C>T maps to NM_001040167.1 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr7:2565889 C>T maps to NM_001040167.1 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr22:38073012 G>A maps to NM_002305.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr19:40096006 C>T maps to NM_013268.2 Y94Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr19:40197835 G>A maps to NM_203471.1 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr19:39281454 G>A maps to NM_001042507.3 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr17:25967774 C>T maps to NM_009587.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr17:20354868 C>T maps to ENST00000324290 Q283Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr17:18394612 G>A maps to NM_001040078.2 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr10:95552643 G>C maps to NM_005097.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:25005687 G>C maps to NM_018176.3 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:25005549 G>A maps to NM_018176.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr8:22006251 G>C maps to NM_139278.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr8:22011488 C>G maps to NM_139278.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr11:27395159 C>T maps to NM_018490.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:27389569 G>A maps to NM_018490.2 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr11:27402439 A>G did not map to a codon.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr11:27389695 G>T maps to NM_018490.2 C858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr11:27405923 C>G maps to NM_018490.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr11:27398721 G>T maps to NM_018490.2 C364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr11:27389578 G>A maps to NM_018490.2 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:71977787 G>A maps to NM_003667.2 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr12:71833916 G>A maps to NM_003667.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr12:71918200 C>T maps to NM_003667.2 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:71960692 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:71960474 G>A maps to NM_003667.2 E331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:71978156 T>C maps to NM_003667.2 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr1:202270045 G>A maps to NM_001017403.1 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr1:202194617 G>T maps to NM_001017403.1 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:202273725 G>C maps to NM_001017403.1 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:202278241 G>A maps to NM_001017403.1 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:202283964 G>T maps to NM_001017403.1 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr6:63990549 G>A maps to NM_016571.2 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:206782759 A>C maps to NM_006893.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:206772965 C>T maps to NM_006893.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr19:49519530 G>A maps to NM_000894.2 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:49519549 C>T maps to NM_000894.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr2:48915213 G>A maps to NM_000233.3 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr2:48915339 C>T maps to NM_000233.3 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr5:77806000 G>A maps to NM_005779.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr7:104377169 C>G maps to NM_199000.2 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr6:35773689 C>T maps to NM_182548.3 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr6:35773575 C>G maps to NM_182548.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr6:35773557 C>T maps to NM_182548.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:35773513 C>T maps to NM_182548.3 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:126172786 C>T maps to NM_022126.3 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:126205771 C>A maps to NM_022126.3 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr17:35298105 C>T maps to NM_005568.3 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:35297718 C>T maps to NM_005568.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:35298105 C>T maps to NM_005568.3 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr17:35300097 G>A maps to NM_005568.3 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:126777583 C>T maps to NM_004789.3 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr9:126776373 C>T maps to NM_004789.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr9:139090905 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr9:139090633 C>T maps to NM_014564.3 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:180199687 C>T maps to NM_033343.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:180217471 G>A maps to NM_033343.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:124979461 G>A maps to NM_014368.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr1:197890577 C>T maps to NM_020204.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr1:197898166 G>A maps to NM_020204.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:38484883 G>A maps to NM_002310.5 R862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:38489297 C>T maps to NM_002310.5 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr5:38482026 T>C maps to NM_002310.5 E988E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr19:48634392 G>A maps to NM_000234.1 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:48643249 G>C maps to NM_000234.1 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:33325293 G>A maps to NM_013975.3 G656G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr17:33321329 G>A maps to NM_013975.3 K497K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr13:108861579 C>T maps to NM_001098268.1 E679E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr19:55106714 C>G maps to NM_006863.1 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr19:55107894 A>G maps to NM_006863.1 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:55087421 G>T maps to NM_001130917.1 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr19:55086316 G>T maps to NM_001130917.1 G158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr19:55085837 C>T maps to NM_001130917.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:55086013 C>G maps to NM_001130917.1 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr19:55087359 C>A maps to NM_001130917.1 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr19:55087349 G>T maps to NM_001130917.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr19:55085828 T>A maps to NM_001130917.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:55087517 C>G maps to NM_001130917.1 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr19:55087517 C>G maps to NM_001130917.1 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr19:54803052 C>T maps to ENST00000251375 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr19:54849824 G>C maps to NM_012276.3 S66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:54848848 C>T maps to NM_012276.3 E258E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:54823807 G>A maps to NM_021250.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:54823807 G>A maps to NM_021250.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr19:54746163 G>C maps to ENST00000407860 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr19:54744261 G>A maps to ENST00000419410 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:54746130 C>T maps to ENST00000407860 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr19:54745908 C>T maps to ENST00000407860 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr19:54744749 G>A maps to ENST00000245620 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr19:54744748 C>A maps to ENST00000245620 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:55147017 G>A maps to ENST00000427581 V586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr19:55146143 A>G maps to ENST00000427581 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr19:55143020 C>A maps to ENST00000427581 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:55143113 G>A maps to ENST00000427581 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr19:55143938 C>G maps to ENST00000427581 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr19:55144175 C>A maps to ENST00000427581 S344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr19:54782928 C>T maps to ENST00000391747 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:54780687 G>A maps to ENST00000391747 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:54782817 A>T maps to ENST00000391747 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:54782180 G>A maps to ENST00000391747 Y414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr19:54721343 C>T maps to NM_001081450.1 Q532Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr19:55176286 C>T maps to ENST00000391733 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr19:55179352 G>A maps to ENST00000391733 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr19:54760854 C>G maps to NM_001081442.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr19:51890568 C>T maps to NM_030657.3 W43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:51890571 C>T maps to NM_030657.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:51883514 C>G maps to NM_030657.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:50616214 C>T maps to NM_001113546.1 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr12:50594580 G>A maps to NM_001113546.1 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:50616147 C>A maps to NM_001113546.1 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:50570906 G>C maps to NM_001113546.1 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:50571653 T>A maps to NM_001113546.1 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr12:50571471 G>C maps to NM_001113546.1 S553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr12:50575724 G>A maps to NM_001113546.1 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr12:50616022 G>A maps to NM_001113546.1 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr4:41605907 A>C maps to NM_014988.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:41648876 C>T maps to NM_014988.2 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr3:45637102 C>T maps to NM_014240.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr3:45637109 C>T maps to NM_014240.2 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr20:62369617 C>G maps to NM_017806.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr22:31671195 C>A maps to NM_001031801.1 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr22:31671195 C>T maps to NM_001031801.1 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr22:31668685 G>A maps to NM_001031801.1 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:109300436 G>A maps to NM_001193484.1 E357E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:128412050 G>A maps to NM_017980.4 C126C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:128399646 G>A maps to NM_017980.4 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:128399743 C>A maps to NM_017980.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:26752885 C>G maps to NM_024674.4 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr1:26737973 C>T maps to NM_024674.4 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:36243369 C>G maps to NM_019104.1 S49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr14:74567921 T>C maps to NM_001024674.2 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr14:74567870 C>A maps to NM_001024674.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr4:83858432 C>G maps to NM_194282.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr1:226496864 C>T maps to ENST00000366807 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr1:226421212 G>A maps to ENST00000366807 D569D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr15:77907711 G>A maps to NM_032808.5 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr15:77907516 C>T maps to NM_032808.5 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr9:27949856 G>A maps to NM_152570.1 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:27950486 G>T maps to NM_152570.1 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr9:27950420 C>T maps to NM_152570.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr9:27950350 G>A maps to NM_152570.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr9:27950204 C>T maps to NM_152570.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr19:2290292 G>A maps to NM_001101391.1 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr19:2291481 G>A maps to NM_001101391.1 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:2290277 C>A maps to NM_001101391.1 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:151774211 C>T maps to NM_001004432.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:151774079 G>A maps to NM_001004432.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr15:101112166 G>A maps to NM_001040616.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr10:90988135 G>A maps to NM_000235.2 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:91005538 G>A maps to NM_000235.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr15:58861006 C>G maps to NM_000236.2 S494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr15:58830604 C>T maps to NM_000236.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr19:42914611 G>C maps to NM_005357.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr19:42911596 C>G maps to NM_005357.2 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr19:42931253 T>C maps to NM_005357.2 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr19:42910493 C>T maps to NM_005357.2 G728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:42909685 G>C maps to NM_005357.2 S798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr19:42910511 C>T maps to NM_005357.2 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:42907082 C>G maps to NM_005357.2 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr10:90429680 C>T maps to NM_001198829.1 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr10:90431628 C>T maps to NM_001198829.1 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr10:90427423 G>A maps to NM_001198829.1 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr10:90436018 T>C maps to NM_001198829.1 N324N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr18:47101863 C>T maps to NM_006033.2 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr3:185252790 G>T maps to NM_139248.2 S60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr3:185252790 G>C maps to NM_139248.2 S60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr3:185251380 A>G maps to NM_139248.2 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr3:185226660 G>A maps to NM_139248.2 Q425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:185252774 C>T maps to NM_139248.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr21:15561576 G>A maps to NM_198996.2 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr10:90492003 G>A maps to NM_001080518.1 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:18135877 C>T maps to NM_004140.3 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:18133325 C>T maps to NM_004140.3 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr17:73570735 C>A maps to NM_001031803.1 L1014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:73554289 G>A maps to NM_001031803.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr17:73569201 C>T maps to NM_001031803.1 A856A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:73559177 C>T maps to NM_001031803.1 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:73565354 C>A maps to NM_001031803.1 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr12:66517667 C>T maps to NM_032338.3 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr12:66517631 A>C maps to NM_032338.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr18:57026359 G>A maps to NM_005570.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr15:75111599 C>T maps to NM_021819.2 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr15:75112415 C>T maps to NM_021819.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr15:75117828 C>T maps to NM_021819.2 N488N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:75108986 C>T maps to NM_021819.2 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr5:176765522 G>A maps to NM_006816.2 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr5:176778287 G>T maps to NM_006816.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:176765495 G>A maps to NM_006816.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:97373495 G>A maps to NM_001142292.1 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:49491847 G>A maps to NM_018113.2 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:49494207 G>A maps to NM_018113.2 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:49496678 G>C maps to NM_018113.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:49491763 G>A maps to NM_018113.2 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:70411791 G>A maps to NM_018368.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr6:70386121 C>T maps to NM_018368.3 K517K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr5:36122391 A>G maps to NM_001007527.1 N370N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr5:36137543 C>A did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr5:36137544 T>C did not map to a codon.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr3:8590589 G>A did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr3:8590408 G>A maps to NM_014583.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr3:8609242 C>T maps to NM_014583.2 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr3:8590589 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr16:1004649 C>A maps to ENST00000262301 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr16:920733 G>A maps to ENST00000262301 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr16:920727 C>A did not map to a codon.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr22:50942125 C>T maps to NM_033200.2 E606E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr22:50943512 C>T maps to NM_033200.2 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr3:197707327 C>T maps to NM_001136049.2 N227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr3:197703552 C>T maps to NM_001136049.2 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr3:197707266 C>G maps to NM_001136049.2 S207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:156100506 C>G maps to NM_170707.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:156105708 G>A maps to NM_170707.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:156108869 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr5:126158475 C>T maps to NM_005573.3 Q464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr5:126154822 C>T maps to NM_005573.3 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr19:2433946 G>A maps to NM_032737.2 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr19:2433964 G>A maps to NM_032737.2 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:2434500 C>A maps to NM_032737.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:33886305 G>T maps to NM_005574.3 C102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:16704181 C>A maps to ENST00000441439 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr13:76397777 A>G maps to ENST00000357063 A836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr13:76427231 G>T maps to ENST00000357063 E1387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr13:76378449 A>G maps to ENST00000357063 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr13:76335155 C>G maps to ENST00000357063 S30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:76407224 G>A maps to ENST00000357063 T926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr13:76391401 G>A maps to ENST00000357063 Q614Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr13:76381693 C>G maps to ENST00000357063 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr13:76393543 A>T maps to ENST00000357063 K624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr13:76427351 C>T maps to ENST00000357063 Q1427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr1:201867504 G>A maps to NM_012134.2 Q600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr7:123302398 C>T maps to NM_207163.1 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr7:123302378 C>T maps to NM_207163.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMW-01A-11D-A42E-08 chr7:123302911 T>C maps to NM_207163.1 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr3:69168083 C>T maps to NM_198271.3 Q474Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:69168257 C>T maps to NM_198271.3 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:69168275 G>C maps to NM_198271.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr3:69168491 C>T maps to NM_198271.3 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:97822236 C>T maps to NM_014916.3 F820F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:97823421 C>T maps to NM_014916.3 F1215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:97821645 C>T maps to NM_014916.3 H623H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr7:97822686 G>A maps to NM_014916.3 S970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr7:97823391 G>A maps to NM_014916.3 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr7:97823451 C>T maps to NM_014916.3 L1225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr19:49000752 G>A maps to NM_001080434.1 L1220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:49000752 G>A maps to NM_001080434.1 L1220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr19:49013406 C>T maps to NM_001080434.1 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:49004779 C>T maps to NM_001080434.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr1:165175151 G>A maps to NM_177398.3 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:165173198 G>C maps to NM_177398.3 S356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr9:129453163 G>T maps to NM_001174147.1 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:100174712 G>A maps to ENST00000489752 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:96349454 C>T maps to NM_005575.2 I713I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:96315471 C>A maps to NM_005575.2 S217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr5:96364212 C>T maps to NM_005575.2 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:54424119 G>A maps to NM_032622.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:28141890 G>A maps to NM_153371.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr13:28127505 C>T maps to NM_153371.3 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr13:28124598 A>T maps to NM_153371.3 L603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr13:28130463 C>A maps to NM_153371.3 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:22546306 C>G maps to NM_001135865.1 S668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr16:22545855 C>T maps to NM_001135865.1 Q518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr16:22545855 C>T maps to NM_001135865.1 Q518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr5:135188349 C>T maps to ENST00000420621 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr5:135188250 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr2:96906261 G>A maps to NM_001037228.1 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:96906059 G>C did not map to a codon.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr2:96906234 T>A maps to NM_001037228.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr2:96906135 C>T maps to NM_001037228.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:40172146 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr19:19258566 C>T maps to ENST00000410050 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr16:20860750 G>C maps to NM_030941.2 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr16:20818355 G>A maps to NM_030941.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:12588634 C>T maps to NM_058169.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr12:12588568 G>A maps to NM_058169.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr19:5707773 G>A maps to NM_004793.2 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:5719792 G>A maps to NM_004793.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:5693377 G>T maps to NM_004793.2 A878A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:5694464 G>A maps to NM_004793.2 F751F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr19:5692057 C>T maps to NM_004793.2 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr16:48290564 G>A maps to NM_031490.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:48290642 G>A maps to NM_031490.2 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:48286110 G>A maps to NM_031490.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr16:48382161 C>A maps to NM_031490.2 A766A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:48329967 C>T maps to NM_031490.2 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:48368169 C>T maps to NM_031490.2 I613I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:12583268 G>A maps to NM_152271.3 F710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr8:12583372 C>A maps to NM_152271.3 E676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr2:100919381 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr23:118124520 G>C did not map to a codon.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr23:118109239 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr23:118109164 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr23:118148220 C>T did not map to a codon.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr1:153233496 C>T maps to NM_000427.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr5:121405765 G>C maps to NM_002317.5 S410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr15:74219678 C>T maps to NM_005576.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr8:23185980 C>T maps to NM_002318.2 W355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr8:23177556 C>T maps to NM_002318.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr8:23156439 G>A maps to NM_002318.2 F718F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:74779554 G>A maps to NM_032603.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:74763221 G>C maps to NM_032603.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:74762467 G>C maps to NM_032603.2 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr2:74776494 C>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:100022548 G>A maps to NM_032211.6 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr6:161007550 C>T maps to NM_005577.2 V1353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr9:113704127 G>C maps to NM_057159.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr19:19737748 G>A maps to NM_004720.5 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:85331293 G>A maps to NM_012152.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:85279606 G>A maps to NM_012152.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:78011464 G>T did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:78010590 T>A did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:78010793 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:78011237 T>G did not map to a codon.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr13:48985927 A>C maps to NM_005767.5 L211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:48985611 G>A maps to NM_005767.5 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr13:48985611 G>A maps to NM_005767.5 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr13:48986487 G>A maps to NM_005767.5 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr13:48985569 T>C maps to NM_005767.5 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr13:48985611 G>A maps to NM_005767.5 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr13:48985611 G>A maps to NM_005767.5 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr13:48985611 G>A maps to NM_005767.5 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr13:48985728 G>A maps to NM_005767.5 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr5:1463831 G>A maps to NM_024830.3 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr5:1466948 G>C maps to NM_024830.3 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr16:55616990 C>G maps to NM_017839.4 S539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:7090194 C>T maps to NM_005768.5 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr12:7086831 G>A maps to NM_005768.5 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr15:34651889 G>A maps to NM_153613.2 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr15:34654787 C>T maps to NM_153613.2 Q290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:211966440 C>T maps to NM_014873.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:14273686 G>T maps to NM_001008701.2 S314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr19:14268692 C>T did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:14271010 C>G maps to NM_001008701.2 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr19:14270343 C>T maps to NM_001008701.2 W636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:82451024 C>G maps to ENST00000370717 S1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:82432118 G>A maps to ENST00000370717 R721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:82434965 C>T maps to ENST00000370717 F872F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr1:82447615 C>T maps to ENST00000370717 Q1091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr1:82372888 C>T maps to ENST00000370717 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:82421723 C>G maps to ENST00000370717 S662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:82409445 T>C maps to ENST00000370717 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr4:62778439 C>T maps to ENST00000506720 Q693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr4:62598941 C>T maps to ENST00000506720 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr4:62863950 G>A maps to ENST00000506720 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:62758518 C>T maps to ENST00000506720 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:62800637 G>C maps to ENST00000506720 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr4:62599225 C>T maps to ENST00000506720 H451H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr4:62863950 G>A maps to ENST00000506720 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr4:62775456 G>A maps to ENST00000506720 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr4:62800706 G>A maps to ENST00000506720 K754K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr4:62542621 C>T maps to ENST00000506720 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr4:62849138 C>T maps to ENST00000506720 F1018F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr4:62800643 G>T maps to ENST00000506720 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr4:62863980 C>T maps to ENST00000506720 I1131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr4:62862018 C>T maps to ENST00000506720 R1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr2:11925029 C>T maps to ENST00000396099 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:11911646 G>A maps to ENST00000396099 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr2:11911613 G>A maps to ENST00000396099 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr18:2920389 G>A maps to NM_014646.2 L864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr18:2921614 G>A maps to NM_014646.2 F786F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr20:39986943 C>T maps to NM_022896.1 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr20:39987107 G>A maps to NM_022896.1 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr8:19818561 G>A maps to NM_000237.2 K430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr8:19805689 G>C did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr3:188242481 G>A maps to NM_005578.3 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr3:188478033 T>A maps to NM_005578.3 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:104048462 G>A maps to NM_017753.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr19:11472106 C>T maps to NM_001170635.1 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:814709 G>A maps to NM_024888.1 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr1:99771794 C>T maps to NM_014839.4 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:99772548 C>A maps to NM_014839.4 R759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:99772406 C>T maps to NM_014839.4 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr1:99771656 C>T maps to NM_014839.4 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr1:99771401 C>T maps to NM_014839.4 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:99387499 G>A maps to NM_001037317.1 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr1:99380452 G>A maps to NM_001037317.1 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:99470137 G>A maps to NM_001037317.1 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr4:155665531 C>G maps to NM_004744.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr4:155665888 C>G maps to NM_004744.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr4:151729480 G>C maps to NM_006726.3 S1792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr4:151827515 G>C maps to NM_006726.3 S512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:151223936 C>T maps to NM_006726.3 L2630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr4:151357946 G>A maps to NM_006726.3 Q2295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr4:151773883 G>C maps to NM_006726.3 S993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr4:151223903 G>A maps to NM_006726.3 V2641V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr4:151829820 G>C maps to NM_006726.3 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:47263285 G>C maps to NM_001164211.1 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:114419092 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr23:114357121 G>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:114404907 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:197598340 G>C maps to NM_032773.2 *713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr3:197562662 G>A maps to ENST00000425562 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:197562591 G>T maps to ENST00000425562 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr7:100172855 C>G maps to NM_002319.3 V642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr7:100180044 C>T maps to NM_002319.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr11:800220 C>T maps to NM_145886.3 V728V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:39805358 G>A maps to NM_020862.1 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr19:39805226 G>A maps to NM_020862.1 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:39804677 G>C maps to NM_020862.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:40399706 G>C maps to NM_020737.1 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr6:40360392 G>A maps to NM_020737.1 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:40399931 T>G maps to NM_020737.1 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr6:40360603 G>C maps to NM_020737.1 S483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:36430719 C>T maps to NM_024509.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr19:36430974 G>A maps to NM_024509.1 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:36431142 C>A maps to NM_024509.1 C272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr19:36430341 G>T maps to NM_024509.1 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:66627176 C>A maps to NM_024036.4 C473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:66627251 C>A maps to NM_024036.4 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:66627353 C>G maps to NM_024036.4 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:66627410 C>G maps to NM_024036.4 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:66625619 C>T maps to NM_024036.4 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr14:42361124 C>T maps to NM_152447.3 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr14:42355857 C>T maps to NM_152447.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr14:42356265 C>G maps to NM_152447.3 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr14:42356472 C>T maps to NM_152447.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr14:42360854 C>T maps to NM_152447.3 H596H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:4538476 C>T maps to NM_052972.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr7:133812299 C>A maps to NM_144648.1 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr7:133812125 G>A maps to NM_144648.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr7:133884159 G>A maps to NM_144648.1 E578E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:133861779 G>T maps to NM_144648.1 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr7:133884060 G>A maps to NM_144648.1 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr7:133876488 G>T maps to NM_144648.1 E473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:133868483 A>G did not map to a codon.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr7:133812146 G>A maps to NM_144648.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:66449392 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:66433415 G>C maps to NM_015541.2 V827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:66444593 G>A maps to NM_015541.2 C446C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:66449419 G>A maps to NM_015541.2 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:66434682 G>A maps to NM_015541.2 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:66448549 C>T maps to NM_015541.2 K430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:66436600 C>T maps to NM_015541.2 K531K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:113638960 T>C maps to NM_014813.1 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr1:113637016 C>G maps to NM_014813.1 S191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:113637016 C>G maps to NM_014813.1 S191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:113638567 C>G maps to NM_014813.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr10:85993979 C>T maps to NM_015613.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr10:85984110 C>T maps to NM_001017924.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr10:85984761 C>G maps to NM_001017924.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr4:110790864 C>A maps to NM_198506.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr4:110790916 G>T maps to NM_198506.2 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr4:110791182 G>A maps to NM_198506.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr4:110789061 C>A maps to NM_198506.2 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr12:25256982 C>A maps to ENST00000354454 S402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr12:25236369 T>C maps to ENST00000354454 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr12:25249924 C>T maps to ENST00000354454 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr12:57588462 C>T maps to NM_002332.2 G2724G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr12:57552203 C>T maps to NM_002332.2 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:57603646 C>T maps to NM_002332.2 P4145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:57586682 C>T maps to NM_002332.2 L2495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:57592286 C>T maps to NM_002332.2 I3170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:57598265 C>T maps to NM_002332.2 G3675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr12:57556104 G>T maps to NM_002332.2 V736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:57578201 C>T maps to NM_002332.2 I2051I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr12:57588212 C>G maps to NM_002332.2 L2665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr12:57552350 C>T maps to NM_002332.2 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr12:57604651 C>G maps to NM_002332.2 R4302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr12:57599380 C>G maps to NM_002332.2 L3837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr12:57591392 G>A maps to NM_002332.2 V3076V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr14:23344693 C>T maps to NM_014045.3 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr14:23344360 C>T maps to NM_014045.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr14:23346424 G>T maps to NM_014045.3 E611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr14:23344897 G>A maps to NM_014045.3 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr14:23345536 G>A maps to NM_014045.3 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr6:150158564 G>A maps to NM_032832.5 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:150174189 G>A maps to NM_032832.5 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:105509411 G>A maps to NM_013437.4 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr8:105507361 C>T maps to NM_013437.4 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr2:142237983 G>A maps to NM_018557.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:141130655 A>C maps to NM_018557.2 G3563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr2:141598562 G>A maps to NM_018557.2 L1680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:141093287 C>T maps to NM_018557.2 L4004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:142888274 T>C maps to NM_018557.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr2:141812760 G>A maps to NM_018557.2 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:141259354 G>A maps to NM_018557.2 G2917G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr2:141986992 T>C maps to NM_018557.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr2:141458068 C>G maps to NM_018557.2 L2183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:141533802 C>T maps to NM_018557.2 K1788K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:140990859 T>C maps to NM_018557.2 L4565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr2:141079601 A>T maps to NM_018557.2 S4190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:141130706 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr2:141660609 C>T maps to NM_018557.2 V1215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr2:141459332 G>C maps to NM_018557.2 V2128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr2:141283902 C>A maps to NM_018557.2 T2593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr2:141116513 G>C maps to NM_018557.2 V3711V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr2:169994003 C>G did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:170083084 G>A maps to NM_004525.2 F1747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr2:170042307 G>A maps to NM_004525.2 R3184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:170148822 G>A maps to NM_004525.2 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:170093703 C>A maps to NM_004525.2 E1534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr2:170003312 G>A maps to NM_004525.2 F4249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr2:170011071 G>A maps to NM_004525.2 R4065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:170042413 C>T maps to NM_004525.2 R3148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:170050364 C>T maps to NM_004525.2 K2912K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr2:170063719 C>T maps to NM_004525.2 L2170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr2:169999205 C>T maps to NM_004525.2 G4362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr2:170063206 G>C maps to NM_004525.2 V2341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr2:170063488 G>A maps to NM_004525.2 Y2247Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:170113632 C>T did not map to a codon.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr19:33697223 G>A maps to NM_002333.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:46917827 C>T maps to ENST00000256991 Q372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr11:46920515 G>A maps to ENST00000256991 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:46895137 T>C maps to ENST00000256991 A1457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr11:68174202 C>T maps to NM_002335.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr11:68191072 C>T maps to NM_002335.2 I1048I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr11:68181361 C>T maps to NM_002335.2 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr11:68157441 C>T maps to NM_002335.2 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr11:68207302 G>T maps to NM_002335.2 G1469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr11:68191087 G>A maps to NM_002335.2 L1053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:25747767 A>T maps to NM_001135772.1 *253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:25756050 G>A maps to NM_001135772.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr12:12300301 G>C maps to NM_002336.2 S1132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:12397409 C>A maps to NM_002336.2 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:12318082 C>T maps to NM_002336.2 E564E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr12:12300490 C>G did not map to a codon.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr12:12318021 G>A maps to NM_002336.2 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:12302024 G>C maps to NM_002336.2 L1019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:12302024 G>A maps to NM_002336.2 L1019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr12:12301925 C>G maps to NM_002336.2 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr12:12311925 C>T maps to NM_002336.2 V876V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:53755275 C>T maps to NM_004631.3 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:53724123 C>G maps to NM_004631.3 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr4:3516517 G>A maps to NM_002337.2 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr2:44209478 G>A maps to NM_133259.3 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:44176791 C>A maps to NM_133259.3 E562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:44170905 C>T maps to NM_133259.3 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:53785423 G>A maps to NM_018214.4 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr12:70003976 C>T maps to NM_201550.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr8:145745404 C>G maps to NM_014665.2 S99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr8:145746447 C>T maps to NM_014665.2 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr5:195110 C>A maps to NM_001080478.1 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr5:195401 T>G maps to NM_001080478.1 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr5:195452 C>G maps to NM_001080478.1 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr3:194080554 G>C maps to NM_001135057.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr3:194080554 G>A maps to NM_001135057.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr14:24535665 C>T maps to NM_138360.3 D1195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr14:24523301 G>A maps to NM_138360.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr14:24523497 C>T maps to NM_138360.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr14:24529268 G>A maps to NM_138360.3 Q653Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr7:102574389 C>G maps to NM_001031692.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr10:50121795 G>A maps to NM_001006939.3 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:26999665 G>C maps to NM_022901.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr12:7014917 G>T maps to NM_201650.2 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:7015815 G>A maps to NM_201650.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr8:145749908 G>A maps to NM_001024678.3 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr8:145748395 G>T maps to NM_001024678.3 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:18507659 G>A maps to NM_145256.2 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:18502811 C>T maps to NM_145256.2 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr19:18502901 G>A maps to NM_145256.2 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:99828119 C>T maps to NM_144598.2 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr15:99796161 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:99926305 G>A maps to NM_144598.2 *368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr16:67242310 A>G maps to NM_001004055.1 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:7232011 C>T maps to NM_001105581.1 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr18:7231327 C>T maps to NM_001105581.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr18:7231978 G>A maps to NM_001105581.1 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr18:7231444 G>A maps to NM_001105581.1 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr3:169574559 T>C maps to NM_024727.2 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr3:169572605 G>T maps to NM_024727.2 S329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:76371367 G>A maps to NM_001128922.1 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr3:196386909 G>A maps to NM_198565.1 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr3:196388271 G>A maps to NM_198565.1 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr3:196386657 C>A maps to NM_198565.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:169524704 G>T maps to NM_001172779.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr3:169511423 C>T maps to NM_001172779.1 *465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr16:67400954 C>T maps to NM_018296.5 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:44630809 C>T maps to NM_001006607.2 F1618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr17:44626215 C>T maps to NM_001006607.2 F1237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr17:62865264 G>A maps to NM_199340.2 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr17:62865277 G>C maps to NM_199340.2 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr17:62856222 C>A maps to NM_199340.2 A1347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr17:62856300 G>A maps to NM_199340.2 V1321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:62864605 G>A maps to NM_199340.2 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr17:62864654 C>G did not map to a codon.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr17:62892232 C>T maps to NM_199340.2 E381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:62893333 G>A maps to NM_199340.2 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr17:62892304 G>A maps to NM_199340.2 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr17:30348422 G>C maps to ENST00000327564 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr17:30376295 C>G maps to ENST00000327564 L880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:30349823 C>T maps to ENST00000327564 Y580Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr17:30358395 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr17:30361940 C>T maps to ENST00000327564 R690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr1:100618080 C>G did not map to a codon.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr7:127670540 C>T maps to NM_022143.4 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr7:127670471 G>C maps to NM_022143.4 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr7:127670602 G>A maps to NM_022143.4 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr7:127670588 G>A maps to NM_022143.4 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr7:127670495 G>C maps to NM_022143.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:70618117 G>C maps to NM_017768.4 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr1:70616830 C>T maps to NM_017768.4 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr1:70614210 G>C maps to NM_017768.4 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:46763282 C>T maps to ENST00000254454 W81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:46751934 G>C maps to ENST00000254454 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:46768813 G>A maps to ENST00000254454 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:46751787 G>A maps to ENST00000254454 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr1:46747008 G>C maps to ENST00000254454 S493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr1:46745287 T>C did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr1:46751603 C>A maps to ENST00000254454 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:54428057 C>T maps to NM_052940.3 C301C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:54426098 C>T maps to NM_052940.3 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:54426040 C>G maps to NM_052940.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr12:122669238 G>A maps to NM_001098519.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:79988620 G>A maps to NM_144999.2 Q651Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr17:45913411 G>A maps to NM_033413.3 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr17:45913815 G>A maps to NM_033413.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:3703762 C>A maps to NM_020710.2 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:3697774 G>A maps to NM_020710.2 D543D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr15:71256226 C>T maps to NM_017691.3 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr15:71256171 C>T maps to NM_017691.3 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr15:71341839 G>A maps to NM_017691.3 Q650Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:51022507 G>A maps to NM_001080457.1 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr19:51021499 C>T maps to NM_001080457.1 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr19:51022624 C>T maps to NM_001080457.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:40137464 G>A maps to NM_020929.1 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr11:40136624 G>A maps to NM_020929.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr11:40136306 T>G maps to NM_020929.1 I512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:40136114 C>A maps to NM_020929.1 T576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr16:84211434 G>A maps to NM_178452.4 P722P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr16:84199454 G>A maps to NM_178452.4 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr16:84209559 G>T maps to NM_178452.4 E574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:165513700 G>T maps to NM_001005214.3 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr1:165532871 C>T maps to NM_001005214.3 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:165532805 G>A maps to NM_001005214.3 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:165533027 G>A maps to NM_001005214.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr1:165513718 G>A maps to NM_001005214.3 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr1:165513715 C>T maps to NM_001005214.3 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr11:554044 G>A maps to NM_198075.3 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr11:552574 C>T maps to NM_198075.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr15:42840304 C>A maps to NM_153260.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr3:120067673 G>A maps to NM_001099678.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:48460408 G>A maps to NM_018509.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr17:48462536 G>C maps to NM_018509.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:48465459 G>A maps to NM_018509.3 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr8:133595957 T>C maps to ENST00000250173 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr8:133645074 C>T maps to ENST00000250173 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr8:133645150 G>T maps to ENST00000250173 S163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr7:150034004 C>T maps to NM_023942.2 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr4:52883313 G>A maps to NM_001024611.1 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr4:52861765 A>G maps to NM_001024611.1 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr4:52861828 C>T maps to NM_001024611.1 E453E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr4:52883386 A>G maps to NM_001024611.1 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr4:52883350 G>A maps to NM_001024611.1 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:67929975 G>A maps to ENST00000421742 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:70488896 G>A maps to NM_020794.2 W507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr1:70482146 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr1:70504818 C>T maps to NM_020794.2 I1066I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr1:70291506 T>C maps to NM_020794.2 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:70504959 G>A maps to NM_020794.2 L1113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr1:70504188 C>T maps to NM_020794.2 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:70503885 T>A maps to NM_020794.2 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:70503870 T>C maps to NM_020794.2 N750N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr1:70446111 T>C maps to NM_020794.2 N216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:70478655 G>A did not map to a codon.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr9:131669701 C>T maps to NM_001127244.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr9:131670420 C>T maps to NM_001127244.1 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr9:131671080 C>G maps to NM_001127244.1 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr9:131670663 C>T maps to NM_001127244.1 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr9:131671305 C>T maps to NM_001127244.1 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr9:131671341 C>A maps to NM_001127244.1 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:131670864 G>A maps to NM_001127244.1 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr9:131670444 C>T maps to NM_001127244.1 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr1:90049006 C>T maps to NM_015350.2 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr1:90049855 C>G maps to NM_015350.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:90179370 G>A maps to NM_032270.4 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:90400468 A>G maps to NM_001134479.1 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:90399550 T>C maps to NM_001134479.1 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:90398746 C>A maps to NM_001134479.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:7960595 C>G maps to NM_025061.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:7964513 C>T maps to NM_025061.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr19:7964183 G>A maps to NM_025061.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:7965380 C>G maps to NM_025061.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:7964520 C>T maps to NM_025061.3 Q372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr19:7963811 C>T maps to NM_025061.3 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:7964330 C>G maps to NM_025061.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr8:86049846 T>C maps to NM_033402.4 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr2:238626427 A>G maps to ENST00000391999 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr2:238664805 G>A maps to NM_001137552.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr2:238671321 G>A maps to NM_001137552.1 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:37105246 C>A maps to NM_006309.2 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr12:85450508 A>G maps to NM_001079910.1 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr12:85459087 C>T maps to NM_001079910.1 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:85547823 T>C maps to NM_001079910.1 L1558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:85449602 G>A maps to NM_001079910.1 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:85466778 C>T maps to NM_001079910.1 V930V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:85517895 G>A maps to NM_001079910.1 K1202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:85492705 C>G maps to NM_001079910.1 S1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr12:85450710 A>T maps to NM_001079910.1 K714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:74492541 C>T maps to NM_001105659.1 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:74507266 G>A maps to NM_001105659.1 R450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:169539713 C>G maps to NM_001080460.1 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:169539936 C>G maps to NM_001080460.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr3:169540563 C>G maps to NM_001080460.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:169539843 C>T maps to NM_001080460.1 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr3:169540296 C>T maps to NM_001080460.1 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr3:169540009 C>T maps to NM_001080460.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr3:169540614 G>C maps to NM_001080460.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr3:169540299 G>A maps to NM_001080460.1 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr3:169540050 C>T maps to NM_001080460.1 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr3:169540083 C>G maps to NM_001080460.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr15:101566279 C>G maps to NM_024652.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr15:101595286 T>A maps to NM_024652.3 L1397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr15:101550735 G>A maps to NM_024652.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr15:101554531 C>T maps to NM_024652.3 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr12:40716968 C>G maps to NM_198578.3 L1839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr12:40699616 C>T maps to NM_198578.3 L1270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:40696684 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr12:40728860 C>T maps to NM_198578.3 A1950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr12:40728839 G>C maps to NM_198578.3 R1943R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr12:40646726 G>A maps to NM_198578.3 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr12:40699704 T>A maps to NM_198578.3 L1299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:40629490 G>A maps to NM_198578.3 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:40643637 C>T maps to NM_198578.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:40713788 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr12:40677748 C>T maps to NM_198578.3 R772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr12:40692964 A>G maps to NM_198578.3 L1134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr3:3887308 C>A maps to NM_020873.5 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr3:3886768 C>G maps to NM_020873.5 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr3:3887742 C>G maps to NM_020873.5 S473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr3:3887650 G>A maps to NM_020873.5 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr3:3888131 C>T maps to NM_020873.5 Q603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:204587881 G>A maps to NM_201630.1 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr1:204588538 G>A maps to NM_201630.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr1:204588348 C>A maps to NM_201630.1 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr7:110764584 C>G maps to NM_018334.4 S586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:6025247 G>C maps to NM_152611.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr20:6021796 G>A maps to NM_152611.3 T698T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr20:6022006 G>A maps to NM_152611.3 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr20:6021775 G>C maps to NM_152611.3 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr2:80529674 G>A maps to NM_178839.4 Q424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:80529639 G>A maps to NM_178839.4 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr2:80530713 G>A maps to NM_178839.4 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:80530005 C>T maps to NM_178839.4 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr2:80530752 C>A maps to NM_178839.4 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr2:80530557 G>T maps to NM_178839.4 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:80529573 G>T maps to NM_178839.4 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMJ-01A-11D-A42E-08 chr2:80530671 G>T maps to NM_178839.4 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:138208712 C>A maps to NM_015564.2 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr10:68687369 G>A maps to NM_178011.3 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr10:68688158 G>A maps to NM_178011.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr10:68687864 G>A maps to NM_178011.3 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr2:77745875 C>A maps to NM_001134745.1 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:77745830 G>T maps to NM_001134745.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:77745524 A>T maps to NM_001134745.1 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:77746265 G>A maps to NM_001134745.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr9:130263352 G>A maps to NM_001005374.2 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr9:130221350 G>T did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr9:130265176 G>A maps to NM_001005374.2 *724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr9:130265126 G>A maps to NM_001005374.2 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr3:54958789 G>A maps to NM_020678.2 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:1943829 G>A maps to NM_001163926.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr12:1940218 G>T maps to NM_001163926.1 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr12:1940230 G>A maps to NM_001163926.1 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr12:1940431 G>A maps to NM_001163926.1 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:1940448 C>A maps to NM_001163926.1 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr11:71806564 G>A maps to NM_145309.2 *193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:71806016 G>C maps to NM_145309.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr7:102113217 C>T maps to NM_152892.1 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr3:115738452 G>A maps to NM_002338.3 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:194371613 G>C maps to NM_018385.2 S472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr3:194362863 C>T maps to NM_018385.2 W637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr8:38021253 C>T maps to NM_014462.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr1:36859514 G>C maps to NM_032881.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:157171171 G>A maps to NM_173491.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr17:42117555 G>A maps to ENST00000411445 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr19:34710341 G>A maps to NM_001114093.1 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr19:34706097 C>G maps to NM_001114093.1 S203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr19:34685410 G>A maps to NM_001114093.1 P50P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FJ-A3Z7-01A-12D-A23M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr20:60706475 C>T maps to NM_144703.2 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:31765793 G>C maps to NM_021177.3 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:18420560 G>A maps to NM_012321.3 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr19:2328461 C>T maps to NM_016199.2 K7K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:7760450 G>A maps to NM_032356.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:35758033 C>G maps to NM_205834.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr19:35739843 C>T maps to NM_205834.2 H21H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:35758630 C>G maps to NM_205834.2 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:35758180 C>T maps to NM_205834.2 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr21:47639461 C>T maps to NM_002340.5 W192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr12:21242856 C>T maps to ENST00000381541 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr12:21176198 G>A maps to ENST00000381541 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr12:21168673 C>T maps to ENST00000381541 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr12:21174487 T>C maps to ENST00000381541 N125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:96421236 G>A maps to NM_000895.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr14:24785315 C>G maps to NM_181657.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr14:24780290 C>T maps to ENST00000336557 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr14:24780919 G>A maps to ENST00000336557 E381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr2:33359989 T>C maps to ENST00000354476 H388H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:33412109 C>T maps to ENST00000354476 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:33614356 C>T maps to ENST00000354476 P1607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr2:33534595 C>T maps to ENST00000354476 Q1194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:33468839 C>G maps to ENST00000354476 S663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr2:33534499 G>C did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr2:33482534 G>A maps to ENST00000354476 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr2:33567999 C>T maps to ENST00000354476 Q1277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr2:33500048 C>T maps to ENST00000354476 Q922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr2:33614362 C>T maps to ENST00000354476 F1609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr14:75017810 G>A maps to NM_000428.2 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr14:74976494 G>A maps to NM_000428.2 F1073F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:74970000 G>A maps to NM_000428.2 R1603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMW-01A-11D-A42E-08 chr14:74975939 C>G did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr11:65318915 C>T maps to NM_001130144.2 Q526Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr11:65315516 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:65308408 G>C maps to NM_001130144.2 L970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr11:65308026 G>A maps to NM_001130144.2 N1012N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr11:65307975 C>T maps to NM_001130144.2 G1029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:41118027 G>A maps to ENST00000308370 V810V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:41132886 C>T maps to ENST00000308370 F1397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr19:41105135 G>A maps to ENST00000308370 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr19:41113415 C>G maps to ENST00000308370 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr19:41135361 C>A maps to ENST00000308370 L1593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr12:6499850 C>T maps to NM_002342.1 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr12:6497639 G>A maps to NM_002342.1 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr12:6499336 C>T maps to NM_002342.1 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr3:46497466 C>T maps to NM_002343.3 Q106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr15:41797424 C>A maps to NM_002344.5 E636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr15:41796247 G>A maps to NM_002344.5 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:144184234 C>T maps to NM_032860.3 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr16:258097 G>A maps to NM_201412.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr16:249117 G>A maps to NM_201412.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr16:249171 G>T maps to NM_201412.1 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:139083367 G>A maps to NM_016019.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:23420483 G>A maps to NM_001142546.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr11:24759794 C>T maps to NM_001009909.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:114541340 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr23:114536556 A>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:114537870 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr3:158386886 G>A maps to NM_020169.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr8:144103079 C>T maps to NM_002346.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr6:31683351 C>T maps to ENST00000375834 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:31685394 C>G maps to ENST00000375834 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr6:31683388 C>T maps to ENST00000375834 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr6:31675388 G>A maps to ENST00000375834 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr6:31675750 G>A maps to ENST00000375834 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr8:144240319 C>T maps to NM_001130478.1 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr8:144240220 G>A maps to NM_001130478.1 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr8:143782007 G>C maps to ENST00000292430 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr2:160710208 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:160667044 G>C maps to NM_001198759.1 S1564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:160698843 G>C maps to NM_001198759.1 L1064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr2:160737659 A>G maps to NM_001198759.1 Y446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:6589065 T>A maps to NM_004271.3 C33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr1:160794029 G>A maps to ENST00000263285 R630R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:160793321 C>G maps to ENST00000263285 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr1:160784450 C>T maps to ENST00000263285 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:160766039 G>A maps to ENST00000263285 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr1:160769711 T>A maps to ENST00000263285 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr2:99912094 C>T maps to NM_174898.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:99901154 C>T maps to NM_174898.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr2:99858935 G>C maps to NM_175735.3 S177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr19:13211528 G>A maps to NM_005583.4 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr8:143856781 C>T did not map to a codon.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr2:133425997 C>T maps to ENST00000409034 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr19:43968549 C>T maps to NM_014400.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:44302739 C>T maps to NM_001031749.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr2:150071148 G>A maps to NM_177964.3 Q183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr2:150061799 C>T maps to NM_177964.3 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:54965250 G>A maps to ENST00000419058 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr5:130522800 G>C maps to NM_181705.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:151134397 G>C maps to NM_212551.4 S120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr5:89814704 G>A maps to NM_198273.1 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:235972028 G>A maps to NM_000081.2 Q697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:235884049 G>A maps to NM_000081.2 F3157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:235920622 G>A maps to NM_000081.2 L2339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:235969822 G>A maps to NM_000081.2 L871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr1:235940492 G>C maps to NM_000081.2 S1777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr1:235973007 C>T maps to NM_000081.2 Q370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr1:235969279 T>C maps to NM_000081.2 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr1:235907457 C>G did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:235887451 G>T maps to NM_000081.2 S3064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr1:235973620 G>C maps to NM_000081.2 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:235969729 G>C maps to NM_000081.2 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:235964227 C>T maps to NM_000081.2 E1294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr1:235826287 C>T maps to NM_000081.2 L3786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr1:235884082 C>T maps to NM_000081.2 L3146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:235972889 G>A maps to NM_000081.2 Q410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:235973316 T>C maps to NM_000081.2 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr12:69746968 C>T maps to NM_000239.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr10:30901800 C>T maps to NM_183058.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr10:30915166 G>A maps to NM_183058.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr10:30900894 C>A maps to NM_183058.2 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:34261800 C>T maps to NM_020426.1 *149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr3:45869963 G>T maps to NM_020347.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr22:21344682 G>A maps to NM_006767.3 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr22:21350311 C>T maps to NM_006767.3 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr22:21345946 C>T maps to NM_006767.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr22:21348901 C>T maps to NM_006767.3 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr22:21350368 C>A maps to NM_006767.3 Y729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:20110393 C>A maps to NM_021020.2 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr8:20110613 G>A maps to NM_021020.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr10:102763274 G>A maps to NM_032429.2 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr10:102765447 G>A maps to NM_032429.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:102763724 T>A maps to NM_032429.2 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr13:36049906 G>A maps to NM_005584.4 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr13:36049659 C>A maps to NM_005584.4 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr13:36049795 C>T maps to NM_005584.4 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr4:151505141 C>T maps to NM_006439.4 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr7:20198185 C>A maps to NM_182762.3 G600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr7:20180730 A>G maps to NM_182762.3 Y799Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr7:20199458 C>T maps to NM_182762.3 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:20199868 C>T did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr7:20198031 G>C maps to NM_182762.3 S651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr7:20193844 G>T maps to NM_182762.3 R773R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr1:39853207 C>G maps to ENST00000361689 L2836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr1:39853306 C>G maps to ENST00000361689 V2869V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr1:39802867 G>A maps to ENST00000289893 R1800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:39827346 C>T maps to ENST00000361689 Q2195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:39801742 A>G maps to ENST00000289893 Q1601Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr1:39765884 G>T maps to ENST00000361689 E834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:39919383 C>T maps to ENST00000361689 F4857F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr1:39854153 G>T maps to ENST00000361689 E3152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:39799982 C>T maps to ENST00000289893 Q1015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr1:39913727 G>C maps to ENST00000361689 L4605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:39800780 G>T maps to ENST00000289893 E1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr1:39853528 C>T maps to ENST00000361689 L2943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:39816506 C>G maps to ENST00000361689 V1610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:39907946 C>G maps to ENST00000361689 L4242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:39800270 C>T maps to ENST00000289893 Q1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:39951249 G>C maps to ENST00000361689 G5359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr1:39824811 G>A did not map to a codon.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr20:14066285 A>G maps to ENST00000310348 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr7:2269701 G>A maps to NM_003550.2 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:11737617 G>C maps to ENST00000376669 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:11740481 G>A maps to ENST00000376669 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr11:47308080 G>C maps to NM_003682.3 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr11:47311755 C>T maps to NM_003682.3 L1020L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr4:1321434 C>G maps to ENST00000505177 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:166973534 C>T maps to NM_032858.1 Y214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr1:166963284 C>T maps to NM_032858.1 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr16:79632823 G>A maps to NM_005360.4 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:144511688 C>T maps to NM_201589.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:39317265 C>T maps to NM_005461.3 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr20:39316779 G>A maps to NM_005461.3 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:39316773 C>T maps to NM_005461.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr22:38610521 C>G maps to NM_012323.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr17:79880792 G>C maps to NM_002359.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr19:35793405 G>A maps to NM_002361.3 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr19:35793579 G>A maps to NM_002361.3 Q400Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr23:152482884 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr23:152482802 A>C did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:151303654 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr23:151303447 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr23:151303837 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr23:151303230 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:151303824 C>T did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:148797575 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:148797575 G>C did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:151899925 T>C did not map to a codon.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr23:151900050 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr23:151900648 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr23:151900074 G>T did not map to a codon.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr23:151900594 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr23:151900153 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr23:151935228 T>A did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr23:151935356 T>C did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr23:151935716 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr23:151935356 T>C did not map to a codon.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr23:151935581 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr23:151092369 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:151092235 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr23:151092925 G>T did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr23:151283721 G>A did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr23:151870003 G>C did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr23:151870054 T>C did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr23:151869718 G>T did not map to a codon.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr23:151870094 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr23:151870249 G>C did not map to a codon.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr23:149013351 T>C did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:149013296 A>T did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr23:30269616 C>G did not map to a codon.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr23:30268919 G>T did not map to a codon.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr23:30269206 G>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:30269468 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr23:30269412 A>G did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr23:27840055 C>T did not map to a codon.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr23:27839429 C>T did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr23:27839489 G>A did not map to a codon.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr23:27839478 G>T did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:27840023 A>G did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:27839618 G>A did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:35820730 T>C did not map to a codon.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr23:35820556 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr23:35820608 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr23:35820878 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr23:35821052 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr23:26157473 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr23:26157111 G>T did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr23:26157993 G>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:26157672 G>T did not map to a codon.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr23:26158022 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr23:26158092 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr23:30237163 C>G did not map to a codon.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr23:30254055 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr23:26212103 T>A did not map to a codon.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr23:26213114 C>T did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr23:26213149 T>A did not map to a codon.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr23:26213117 T>A did not map to a codon.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr23:26212430 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr23:26212473 G>A did not map to a codon.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr23:26212172 T>A did not map to a codon.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr23:26212947 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9SU-01A-31D-A391-08 chr23:26212315 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:26212477 G>T did not map to a codon.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr23:26212039 C>T did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr23:140995584 C>T did not map to a codon.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr23:140993969 T>C did not map to a codon.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr23:140995947 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr23:140995227 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:140994259 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr23:140995413 A>T did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr23:140996130 G>C did not map to a codon.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr23:140996491 C>A did not map to a codon.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr23:140995898 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr23:140995721 G>C did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr23:140993441 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr23:140995818 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr23:140996206 T>C did not map to a codon.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr23:140996090 A>C did not map to a codon.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr23:140993237 G>C did not map to a codon.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr23:140995383 C>T did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr23:140994668 T>C did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:140993265 C>T did not map to a codon.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr23:140995260 C>T did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr23:140994868 C>G did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:140994541 T>C did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:140996332 G>T did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:140993636 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr23:140994572 T>G did not map to a codon.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr23:141290840 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:141291071 C>T did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:141291022 C>T did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:141291023 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr23:141290658 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr23:141291224 C>G did not map to a codon.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr23:141290978 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr23:140969236 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr23:140984519 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr23:140969483 C>T did not map to a codon.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr23:140983189 C>G did not map to a codon.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr23:140969349 T>C did not map to a codon.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr23:140984611 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr23:140969331 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr23:140985203 A>G did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:140985340 G>A did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr23:140985119 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:140969486 C>T did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr23:140985380 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:140985108 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:51644765 C>T did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr23:51638298 C>G did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:51637850 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr23:51640907 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr23:54841755 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:54841144 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr23:54841755 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:54836547 C>T did not map to a codon.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr23:54838640 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SU-01A-31D-A391-08 chr23:54839983 G>T did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:75648703 T>C did not map to a codon.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr23:75650836 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr23:75651090 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr23:75649898 C>T did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr23:75649247 C>T did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:75649790 C>A did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:75650074 G>C did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:75650120 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:75650126 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:75650295 G>A did not map to a codon.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr23:75003747 A>G did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:75003929 G>A did not map to a codon.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr23:75004744 G>A did not map to a codon.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr23:75003484 C>A did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:75004684 G>T did not map to a codon.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr23:75004060 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr23:75004495 G>A did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:184429333 C>T maps to NM_022149.4 K92K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:55479291 T>G did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:55479334 C>T did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr15:23889946 G>C maps to NM_019066.4 L981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:23890751 G>T maps to NM_019066.4 S713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr15:23890798 G>C maps to NM_019066.4 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr15:23889340 G>A maps to NM_019066.4 L1183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:65346991 C>T maps to NM_001033057.1 E1172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr3:65464348 G>A maps to NM_001033057.1 Y225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr3:65422832 G>A maps to NM_001033057.1 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr7:77649045 C>T maps to NM_012301.3 A1318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr7:77762249 C>T maps to NM_012301.3 Q1053Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:77649126 T>C maps to NM_012301.3 E1291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr7:77973233 T>G maps to NM_012301.3 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr7:77649120 G>A maps to NM_012301.3 D1293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr7:79082468 G>A maps to NM_012301.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr7:77649003 G>C maps to NM_012301.3 P1332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr7:77973277 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr7:78636424 G>A maps to NM_012301.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:114201795 G>C maps to NM_001142782.1 G908G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:114189164 C>T maps to NM_001142782.1 Q686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:114225877 C>T maps to NM_001142782.1 Q1230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:114123164 C>T maps to NM_001142782.1 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr1:114165616 G>T did not map to a codon.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr1:114162390 A>C maps to NM_001142782.1 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:114196635 A>G maps to NM_001142782.1 P875P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:114128165 T>G maps to NM_001142782.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:114191916 C>T maps to NM_001142782.1 F738F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:114184791 G>A maps to NM_001142782.1 Q540Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr23:49022468 C>G did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr23:49022415 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr23:49021243 A>C did not map to a codon.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr1:53692716 C>T maps to NM_002370.2 *147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:53694614 G>A maps to NM_002370.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:53701307 C>T did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:77150857 G>A did not map to a codon.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr23:77112889 C>T did not map to a codon.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr23:77096781 C>G did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:10803997 G>A maps to NM_005906.3 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr6:10804120 A>C maps to NM_005906.3 Y165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:33346597 G>A maps to NM_032509.3 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr2:95715399 G>A maps to NM_002371.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr2:95715354 C>G maps to NM_002371.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr18:56377296 C>T maps to NM_006785.2 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr18:56363631 A>C maps to NM_006785.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr9:72833323 C>T maps to NM_153267.4 R575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr9:139749432 C>G maps to ENST00000392881 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr9:139754395 C>G maps to ENST00000392881 L1167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr9:139750012 G>A maps to ENST00000392881 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr9:139748774 C>T maps to ENST00000392881 N261N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr9:139752021 C>T maps to ENST00000392881 T853T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr5:179201094 C>G maps to NM_014757.4 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr5:179201772 G>T maps to NM_014757.4 G982G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:96074993 G>C maps to NM_032427.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr11:95712450 G>A maps to NM_032427.1 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr11:95712800 C>A maps to NM_032427.1 G928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:140646941 C>G maps to ENST00000509479 R793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr4:140810588 C>T maps to ENST00000509479 Q667Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr23:149638527 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr23:149639178 C>T did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:149642007 T>C did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr19:49216634 C>G maps to NM_001130915.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:119510943 G>A maps to NM_005907.2 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:118039473 G>A maps to NM_006699.3 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:117944918 G>A maps to NM_006699.3 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr1:117944853 A>T maps to NM_006699.3 K117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr9:139995589 C>G maps to NM_016219.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:26073232 G>T maps to NM_020379.2 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:26104603 G>A maps to NM_020379.2 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr1:26012974 G>A maps to NM_020379.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:109202633 C>T maps to NM_002372.2 Q1124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr15:91456141 C>T maps to NM_006122.2 V835V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr15:91461461 C>A maps to NM_006122.2 L1011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr15:91452613 C>T maps to NM_006122.2 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr15:91447502 C>T maps to NM_006122.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:12758065 G>A maps to NM_000528.3 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:12767435 G>A maps to NM_000528.3 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:12759050 G>A maps to NM_000528.3 Q868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr4:6588792 C>T maps to NM_015274.1 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr4:6610896 G>A maps to NM_015274.1 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr4:6578363 C>T maps to NM_015274.1 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr4:6598885 G>A maps to NM_015274.1 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr4:6578363 C>T maps to NM_015274.1 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr4:6621664 G>A maps to NM_015274.1 Q942Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr15:75656926 C>A maps to NM_006715.2 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr15:75652498 G>A maps to NM_006715.2 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr15:75659975 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr4:103556105 C>A maps to NM_005908.3 E752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr4:103644042 G>A maps to NM_005908.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr4:103611845 G>A maps to NM_005908.3 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr6:96054268 G>A maps to NM_024641.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:38265847 C>T maps to NM_001113482.1 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:51426366 G>A maps to ENST00000273628 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr3:51423654 G>C maps to ENST00000273628 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr12:12483225 G>C maps to NM_018050.2 S344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:43587476 C>A did not map to a codon.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr23:43590544 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:43592036 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr23:43590499 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr23:43552666 T>A did not map to a codon.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr23:43698113 C>A did not map to a codon.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr23:43652675 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr15:43819661 C>T maps to ENST00000382031 P2235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr15:43821417 G>T maps to ENST00000382031 E2821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:43815110 C>T maps to ENST00000382031 V718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr15:43816950 C>T maps to ENST00000382031 Q1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr15:43820097 G>T maps to ENST00000382031 E2381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr15:43821926 G>A maps to ENST00000382031 K2943K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr15:43819226 C>T maps to ENST00000382031 L2090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr15:43815554 G>A maps to ENST00000382031 Q866Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr5:71403525 C>T maps to NM_005909.3 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:71491836 C>T maps to NM_005909.3 T885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr5:71494956 C>G maps to NM_005909.3 T1925T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr5:71494386 T>C maps to NM_005909.3 A1735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr5:71494798 C>T maps to NM_005909.3 Q1873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:172945091 G>A maps to NM_199227.1 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:172928566 C>G maps to NM_199227.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr20:33147572 C>T maps to NM_181509.1 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr20:33147692 C>T maps to NM_181509.1 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr1:242159686 C>G maps to NM_001004343.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:17837422 C>T maps to NM_018174.4 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr19:17836874 G>T maps to NM_018174.4 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:210595045 C>T maps to NM_002374.3 I1803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr2:210557961 C>A maps to NM_002374.3 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr2:210560520 T>C maps to NM_002374.3 D1209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr2:210561030 C>T maps to NM_002374.3 D1379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr2:210559446 T>C maps to NM_002374.3 T851T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr15:66727425 A>T maps to NM_002755.3 K48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:4117503 G>A maps to NM_030662.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:4101064 G>T maps to NM_030662.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr17:21201740 G>A maps to NM_145109.2 K22K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr17:21207741 G>A maps to NM_145109.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr17:21204283 C>T maps to NM_145109.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr17:21208406 C>G maps to NM_145109.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr15:67923240 G>A maps to NM_145160.1 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:67519676 C>T maps to NM_002758.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr17:67521064 C>T maps to NM_002758.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr17:67519676 C>T maps to NM_002758.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:7968918 C>G maps to ENST00000425613 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:7976325 G>A maps to ENST00000425613 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr5:56177955 C>T maps to NM_005921.1 Q977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:56178365 C>T maps to NM_005921.1 F1113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:56178161 C>T maps to NM_005921.1 V1045V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:56189411 C>T maps to NM_005921.1 R1482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr5:56161653 A>T did not map to a codon.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr5:56152510 G>A maps to NM_005921.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr5:56171086 C>T maps to NM_005921.1 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:40715100 C>T maps to NM_002446.3 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr19:40715112 G>A maps to NM_002446.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr19:40715100 C>T maps to NM_002446.3 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr19:40710487 G>A maps to NM_002446.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr11:65375773 C>T maps to NM_002419.3 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr11:65380752 C>A maps to NM_002419.3 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr11:65365762 C>G maps to NM_002419.3 *848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:53878052 G>A maps to NM_001193511.1 Y412Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr12:53877711 C>T maps to NM_001193511.1 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:185191488 C>T maps to NM_004721.3 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr3:185191525 C>T maps to NM_004721.3 R803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr3:185155307 C>T maps to NM_004721.3 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr3:185191449 A>G maps to NM_004721.3 E777E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr3:185155358 G>A maps to NM_004721.3 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:43363962 C>T maps to ENST00000344686 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr17:43345028 C>T maps to ENST00000344686 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:43345028 C>T maps to ENST00000344686 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:19507019 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:19413273 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr23:19482500 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr23:19389507 C>T did not map to a codon.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr23:19389541 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:19387307 C>T did not map to a codon.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr23:19443800 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr23:19506966 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:19449623 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:19449706 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr23:19478198 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr23:19387250 T>C did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:128066316 G>C maps to NM_006609.3 S493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:128075804 T>A maps to NM_006609.3 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr2:128087554 T>C maps to NM_006609.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:128066253 G>C maps to NM_006609.3 S514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr2:128079769 C>G maps to NM_006609.3 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:61767078 G>A maps to NM_203351.1 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:61768565 G>C maps to NM_203351.1 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:61766935 C>T maps to NM_203351.1 Q333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr6:161513085 G>A maps to NM_005922.2 Q1060Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr6:161455435 C>T maps to NM_005922.2 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr6:161491785 T>G maps to NM_005922.2 V618V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:136977456 C>G maps to NM_005923.3 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:137018500 G>C maps to NM_005923.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:136913657 C>T maps to NM_005923.3 L991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr6:136980396 G>A maps to NM_005923.3 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:136882783 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr6:136922961 T>C maps to NM_005923.3 K945K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr6:136923006 G>A maps to NM_005923.3 N930N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr6:136990475 G>A maps to NM_005923.3 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr1:27683575 G>A maps to NM_004672.3 I1096I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:27686746 C>A maps to NM_004672.3 E723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:27686836 C>A maps to NM_004672.3 E693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:27683199 C>T maps to NM_004672.3 L1135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr1:27685223 C>T maps to NM_004672.3 G853G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr1:27683962 C>G maps to NM_004672.3 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr1:27685102 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:91254346 A>C maps to NM_145331.1 Y405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr6:91269805 C>G maps to NM_145331.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:30728106 T>C maps to NM_005204.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr10:30728017 C>T maps to NM_005204.2 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr10:30739296 C>A maps to NM_005204.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr10:30747017 C>T maps to NM_005204.2 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr14:71267618 G>A maps to NM_033141.2 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr14:71199717 C>A maps to NM_033141.2 E804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr14:71216770 C>T maps to NM_033141.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr14:71209104 C>T maps to NM_033141.2 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:47958224 T>C maps to ENST00000426837 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:47950746 G>A maps to ENST00000426837 R1739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:47894728 G>A maps to ENST00000426837 L2270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:47896809 G>A maps to ENST00000426837 F2208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr3:47894424 C>A maps to NM_001134364.1 E1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr3:47956391 C>G maps to ENST00000426837 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr3:48040147 G>C maps to ENST00000426837 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr3:47960220 G>A maps to ENST00000426837 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr3:47950537 C>G maps to ENST00000426837 L1808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr19:39086327 C>A maps to NM_001042600.1 G741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr19:39098538 T>A maps to NM_001042600.1 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr19:39108049 G>T maps to NM_001042600.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr19:39106877 G>A maps to NM_001042600.1 C90C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:39103252 G>C maps to NM_001042600.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr11:64564141 G>A maps to NM_004579.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:39664038 G>A maps to NM_003618.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr2:39552952 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:39499673 G>A maps to NM_003618.2 R602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr2:39536601 A>G maps to NM_003618.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr2:39664074 C>T maps to NM_003618.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:39477776 A>G maps to NM_003618.2 G889G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:39505624 G>A maps to NM_003618.2 Q573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr2:39505627 C>T did not map to a codon.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr2:39552930 A>G maps to NM_003618.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:102440401 G>T maps to NM_145686.2 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:102456340 C>G maps to NM_145686.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr14:50901238 C>T maps to NM_198794.1 V679V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr11:75319252 G>A maps to NM_033063.1 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr11:75319174 T>C maps to NM_033063.1 E366E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:75298604 C>T maps to NM_033063.1 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr11:75298104 C>G maps to NM_033063.1 *814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr11:75379324 G>A maps to NM_033063.1 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr6:136687110 C>T maps to NM_001198609.1 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr6:136667000 C>T maps to NM_001198609.1 Q774Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr6:136699006 C>T did not map to a codon.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr1:36636770 G>A maps to NM_018067.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr1:36640520 G>A maps to NM_018067.3 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BS-01A-21D-A26M-08 chr23:20043940 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr23:20062506 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:20043945 C>G did not map to a codon.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr23:135313899 C>T did not map to a codon.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr23:135328279 T>C did not map to a codon.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr23:135303036 T>G did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr22:22161969 G>A maps to NM_138957.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:87023142 C>T maps to NM_138982.2 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr4:87080491 C>T maps to NM_138982.2 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr4:87022229 G>A maps to NM_138982.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr4:87028486 G>A maps to NM_138982.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr22:50705387 G>A maps to NM_002751.5 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr22:50695569 C>A maps to NM_002969.3 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:36106812 C>T maps to NM_002754.3 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:36020526 C>T maps to NM_139012.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr6:36067963 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr6:36041851 G>C maps to NM_139012.2 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr8:144803971 G>A maps to NM_139021.2 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr8:144803788 G>T maps to NM_139021.2 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr8:144804377 C>A maps to NM_139021.2 S531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr8:144804291 C>T maps to NM_139021.2 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr14:55529992 C>T maps to NM_144578.3 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr16:30134419 G>A maps to NM_002746.2 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:30128084 G>A maps to NM_002746.2 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr16:30128090 G>A maps to NM_002746.2 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr18:48190813 C>G maps to NM_002747.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr18:48190738 C>G maps to NM_002747.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr18:48241510 C>T maps to NM_002747.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr15:52338702 C>T maps to NM_002748.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr17:19284404 C>A maps to NM_139034.2 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr17:19284256 C>G maps to NM_139034.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr10:49634092 C>G maps to NM_139049.1 S284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr11:45926752 C>T maps to NM_005456.2 H672H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:1797073 C>T maps to NM_015133.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:1798632 C>T maps to NM_015133.3 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:1810452 G>T maps to NM_015133.3 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr16:1817830 C>T maps to NM_015133.3 F1144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr16:1817198 G>C maps to NM_015133.3 P1045P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:1817650 G>C maps to NM_015133.3 L1107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr16:1818251 C>T maps to NM_015133.3 I1204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr5:179666935 C>A maps to NM_002752.4 E350*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DK-A3IU-01A-11D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr9:128347886 C>G maps to NM_001006617.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:206904054 G>A maps to NM_032960.2 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr1:206903366 C>T maps to NM_032960.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr3:50684225 C>A maps to NM_004635.3 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr3:50685380 C>T maps to NM_004635.3 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:50685458 G>A maps to NM_004635.3 Q377Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr3:50685413 C>G maps to NM_004635.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr3:50677924 C>T maps to NM_004635.3 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr15:42109189 G>A maps to NM_001128608.1 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr15:42116198 G>T maps to NM_001128608.1 E1391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr15:42110218 C>T maps to NM_001128608.1 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr15:42067505 G>A maps to NM_001128608.1 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr20:31427558 C>G maps to NM_012325.2 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr18:32706972 C>G maps to NM_014268.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr18:32682029 C>T maps to NM_014268.2 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr17:44101516 C>T maps to NM_001123066.3 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr17:44039819 G>A maps to NM_001123066.3 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr17:44060604 G>C maps to NM_001123066.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr17:44049255 A>C maps to NM_001123066.3 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr4:164534482 G>T maps to ENST00000514618 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr17:60799866 C>T maps to NM_152598.2 Q732Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr17:60814067 C>T maps to NM_152598.2 E387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:60799941 G>A maps to NM_152598.2 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:8503336 G>A maps to NM_016496.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr19:8495717 C>T maps to NM_016496.4 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr19:8495726 C>T maps to NM_016496.4 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:126214080 C>T maps to NM_178450.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr2:217124124 G>T maps to NM_020814.2 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:10403538 G>C maps to NM_005885.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr5:10403646 G>C maps to NM_005885.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:160604795 C>G maps to NM_022826.2 S332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr2:160605377 C>G maps to NM_022826.2 S526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr2:160621180 C>G maps to NM_022826.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:58152658 C>T maps to NM_138396.4 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:32800392 G>A maps to NM_023009.5 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:32800503 G>A maps to NM_023009.5 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:119727735 C>G maps to NM_006770.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:119739072 A>T maps to NM_006770.3 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:220752865 C>T maps to NM_018650.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:220792049 C>T maps to NM_018650.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:220825333 G>A maps to NM_018650.3 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:63668427 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr11:63676592 G>T maps to NM_001039469.2 E751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:63668460 G>T maps to NM_001039469.2 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr11:63662743 C>G maps to NM_001039469.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:103969476 G>T maps to ENST00000335102 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:45767942 G>A maps to NM_031417.3 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:45781257 G>A maps to NM_031417.3 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr19:45767972 G>A maps to NM_031417.3 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr19:45783635 G>A maps to NM_031417.3 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr19:45790772 G>T maps to NM_031417.3 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:45774875 C>G maps to NM_031417.3 Y232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr12:57908748 C>T maps to NM_004990.2 A704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr12:57882850 G>A maps to NM_004990.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr5:68728481 C>T maps to NM_001038603.2 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr5:68715298 A>G maps to NM_001038603.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr16:71668135 C>T maps to NM_052858.3 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:71668171 G>A maps to NM_052858.3 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:160328829 C>T maps to NM_002377.2 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:160328241 C>T maps to NM_002377.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:29454595 G>A maps to NM_052967.1 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:29455148 G>A maps to NM_052967.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr6:29455302 G>T maps to NM_052967.1 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr3:186954016 G>A maps to NM_139125.3 Q548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:186969424 C>T maps to NM_139125.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:186961380 C>T maps to NM_139125.3 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:11102930 C>T did not map to a codon.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr1:11097836 A>G maps to NM_006610.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:12958497 G>A maps to NM_014975.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:12969527 C>T maps to NM_014975.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr19:12985092 G>A maps to NM_014975.2 A1374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:12985128 C>T maps to NM_014975.2 V1386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:12954348 C>T maps to NM_014975.2 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:12984212 G>T maps to NM_014975.2 S1113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:12975886 C>T maps to NM_014975.2 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr19:12962830 G>A maps to NM_014975.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:12980031 A>T maps to NM_014975.2 K976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:12969353 C>G maps to NM_014975.2 Y389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr1:46485284 G>A maps to NM_015112.2 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr1:46495136 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:18232506 G>A maps to NM_015016.1 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr19:18235466 G>T maps to NM_015016.1 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr19:18255987 C>T maps to NM_015016.1 I967I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr19:18234407 G>A maps to NM_015016.1 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr5:66396384 G>A maps to NM_001164664.1 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:66462290 G>A maps to NM_001164664.1 P2428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr5:66440573 C>A maps to NM_001164664.1 T936T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr5:66460280 C>G maps to NM_001164664.1 L1758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr5:66459602 G>A maps to NM_001164664.1 L1532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:66460409 C>T maps to NM_001164664.1 I1801I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr5:66456366 G>A maps to NM_001164664.1 K1244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr5:66386047 A>G maps to NM_001164664.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr5:66449323 G>A maps to NM_001164664.1 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr5:66445238 G>A maps to NM_001164664.1 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr5:66440989 C>T maps to NM_001164664.1 S959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr10:27459816 G>A maps to NM_001172303.1 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr10:82043717 C>T maps to NM_000429.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr10:82036335 G>T maps to NM_000429.2 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr10:82043702 G>A maps to NM_000429.2 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr2:85770893 G>A maps to NM_005911.4 *396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:3781623 G>A maps to NM_002378.3 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr19:3779709 C>T maps to NM_002378.3 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr8:98943550 G>C maps to ENST00000254898 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr8:99019342 C>T maps to ENST00000254898 H446H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr8:99047938 G>A maps to ENST00000254898 *958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr8:98973702 C>T maps to ENST00000254898 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr2:20202934 C>T maps to NM_002381.4 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr20:43929793 C>A maps to ENST00000372754 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr5:138654643 T>C maps to ENST00000394800 D452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:138661215 G>T maps to ENST00000394800 E794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr20:3846493 C>T maps to NM_020746.3 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr20:3838391 G>A maps to NM_020746.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr20:3842923 G>A maps to NM_020746.3 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr16:29819027 C>T maps to NM_001042539.1 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr16:29818813 G>C maps to NM_001042539.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47W-01A-11D-A23U-08 chr16:29821443 A>G maps to NM_002383.2 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:29819017 G>A maps to NM_001042539.1 E304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr16:29818738 C>A maps to NM_001042539.1 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr16:29821552 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:29819562 C>G maps to NM_001042539.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:29819574 C>T maps to NM_001042539.1 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:36006936 G>A maps to NM_203377.1 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr22:36003349 C>T maps to NM_203377.1 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr18:47799760 C>T maps to ENST00000424334 W560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr18:47799840 C>A maps to ENST00000424334 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr18:51731412 C>T maps to NM_003927.3 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr18:51731508 G>A maps to NM_003927.3 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr18:51731375 G>A maps to NM_003927.3 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr19:1584562 C>T maps to NM_003926.5 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr3:129150349 T>C maps to NM_003925.1 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:129155754 C>T maps to NM_003925.1 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr3:129155373 C>T maps to NM_003925.1 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:149226995 C>G maps to ENST00000404807 S495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:149240943 G>T maps to ENST00000404807 V928V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr2:149226732 C>G maps to ENST00000404807 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr12:57918190 C>G maps to NM_052897.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr12:57919410 C>T maps to NM_052897.3 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr12:57918740 C>T maps to NM_052897.3 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr12:57919939 C>T maps to NM_052897.3 Q397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr12:57922069 C>G maps to NM_052897.3 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:57920562 G>A maps to NM_052897.3 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr10:54527897 C>T maps to NM_000242.2 *249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr5:89757190 A>G maps to NM_203406.1 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr5:89757256 G>A maps to NM_203406.1 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr13:97986586 C>T maps to ENST00000376673 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr13:97999161 A>G maps to ENST00000376673 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr13:97986693 G>T maps to ENST00000376673 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:131525016 T>A did not map to a codon.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr23:131525069 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:131573562 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr6:20126921 G>A maps to NM_001080480.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr6:20212396 G>A maps to NM_001080480.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr6:20126785 G>A maps to NM_001080480.1 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr2:9083341 G>A maps to NM_138799.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr2:9083347 G>T maps to NM_138799.2 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr19:54692144 G>A maps to NM_024298.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr19:54677812 A>C maps to NM_024298.3 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:54677869 G>A maps to NM_024298.3 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr18:74778341 C>A did not map to a codon.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr18:74692427 C>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr16:84118641 G>C maps to NM_003791.2 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr16:84118641 G>C maps to NM_003791.2 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:84088149 G>A maps to NM_003791.2 I1021I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr16:84108234 G>A maps to NM_003791.2 N520N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr16:84088128 C>T maps to NM_003791.2 P1028P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:84125381 G>A maps to NM_003791.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr16:84092935 C>T maps to NM_003791.2 K934K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr23:21863398 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:21896613 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr23:21861408 G>A did not map to a codon.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr23:21863340 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr23:21896196 C>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr23:21863385 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:89986103 C>T maps to ENST00000304984 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:89986130 C>T maps to ENST00000304984 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr18:13884796 A>G maps to NM_000529.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:54824012 C>A maps to ENST00000371389 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr20:54824541 C>A maps to ENST00000371389 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr18:58038832 C>T maps to NM_005912.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr18:58039270 G>A maps to NM_005912.2 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr18:13826345 C>T maps to NM_005913.2 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr18:13826366 G>A maps to NM_005913.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr18:13826051 C>T maps to NM_005913.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr18:13826333 C>T maps to NM_005913.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:119181613 C>T did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:119182860 C>T maps to NM_006500.2 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:119183624 C>G maps to NM_006500.2 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:119181551 G>A maps to NM_006500.2 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B0-01A-11D-A31L-08 chr23:103349041 G>A did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr22:43539108 G>C maps to NM_173467.4 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr5:112363127 C>T maps to NM_001085377.1 L977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr5:112403813 C>G maps to NM_001085377.1 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr3:182810310 G>C maps to NM_020166.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr3:182759418 T>C maps to NM_020166.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:182769980 G>A maps to NM_020166.3 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr3:182788830 G>A maps to NM_020166.3 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:70900208 C>T maps to NM_022132.4 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr2:71351604 G>A maps to NM_032601.3 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr23:138708449 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr23:138672034 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:138714551 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:138727776 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:138729007 A>C did not map to a codon.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr23:138664662 C>G did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr23:138668583 A>T did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:138669899 G>C did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:138680589 A>G did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:138687883 A>G did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr13:113730362 T>A maps to NM_001112732.1 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr13:113729379 G>A maps to NM_001112732.1 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr13:113678962 C>A maps to NM_001112732.1 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr13:113742939 C>T maps to NM_001112732.1 T1001T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr13:113724430 C>T maps to NM_001112732.1 Q371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:183013199 C>G maps to NM_015078.2 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr3:183041139 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr3:182897405 T>C maps to NM_015078.2 E1060E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr22:41077226 C>T maps to NM_005297.3 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr22:41077322 C>T maps to NM_005297.3 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr22:41077823 C>T maps to NM_005297.3 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:100395768 A>C maps to NM_032503.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr6:100368956 G>C maps to NM_032503.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:100390865 C>T maps to NM_032503.2 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:150550773 G>A maps to NM_021960.4 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr1:150551565 G>A maps to NM_021960.4 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:150551724 C>G maps to NM_021960.4 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr10:13225054 G>A maps to NM_182751.2 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr10:13214464 C>T maps to NM_182751.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:13213024 C>G maps to NM_182751.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr10:13222579 G>A maps to NM_182751.2 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr3:127325533 C>G maps to NM_004526.2 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:127325141 C>T maps to NM_004526.2 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr3:127335796 G>T maps to NM_004526.2 E537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr6:52147487 G>C maps to ENST00000419835 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:52129559 G>C maps to ENST00000419835 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:52137212 G>A maps to ENST00000419835 Y616Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:52129559 G>A maps to ENST00000419835 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr21:47674340 C>T maps to NM_003906.3 P1367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr21:47655202 C>A maps to NM_003906.3 L1974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr21:47663415 C>T maps to NM_003906.3 L1753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr21:47690461 G>A maps to NM_003906.3 F827F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:47660800 G>A maps to NM_003906.3 R1853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr21:47700465 C>T maps to NM_003906.3 K489K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr21:47663415 C>G maps to NM_003906.3 L1753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr8:48887363 C>G maps to NM_182746.1 S736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr8:48874718 G>A maps to NM_182746.1 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr22:35808506 C>T maps to NM_006739.3 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr22:35812628 A>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:136620271 G>A maps to NM_005915.4 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:136626326 G>A maps to NM_005915.4 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr2:136603936 C>T maps to NM_005915.4 V693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr7:99697217 C>T maps to NM_005916.3 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr7:99697265 C>T maps to NM_005916.3 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr7:99695254 G>A maps to NM_005916.3 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:99695469 C>G maps to NM_005916.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:99695481 G>C maps to NM_005916.3 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr7:99695254 G>A maps to NM_005916.3 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr7:99697345 G>A maps to NM_005916.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr7:99691000 C>T maps to NM_005916.3 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr6:119232919 A>G maps to ENST00000316316 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr19:7593840 C>T maps to NM_020533.2 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:7591754 C>T maps to NM_020533.2 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:7590027 C>G maps to NM_020533.2 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr19:7591348 C>T maps to NM_020533.2 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr19:7593585 G>A maps to NM_020533.2 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr19:7591798 G>A maps to NM_020533.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:85498381 C>T maps to NM_018298.9 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr1:85488002 G>A maps to NM_018298.9 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr8:6357450 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr12:49953081 G>A maps to NM_001012300.1 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr12:49956880 G>A maps to NM_001012300.1 H249H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:49959969 C>T maps to NM_001012300.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr5:94275892 T>A maps to NM_024717.4 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:94278071 C>G maps to NM_024717.4 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:94245026 T>C maps to NM_024717.4 E527E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr5:94248603 C>T maps to NM_024717.4 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr5:94208914 C>G maps to NM_024717.4 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr15:94913371 T>G maps to NM_018349.3 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr15:95019958 C>T maps to NM_018349.3 P835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr15:94910953 C>T maps to NM_018349.3 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr15:94882605 G>A maps to NM_018349.3 W242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr15:94945135 C>G maps to NM_018349.3 S658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:94858813 C>G maps to NM_018349.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr15:95022217 C>G maps to NM_018349.3 L864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr23:119742108 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr23:119739340 G>A did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr23:119742149 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr6:30675226 G>C maps to NM_014641.2 L1006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr6:30673314 G>T maps to NM_014641.2 T1215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr6:30680686 G>A maps to NM_014641.2 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr6:30673686 C>T maps to NM_014641.2 E1091E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:30681763 C>T maps to NM_014641.2 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr6:30671643 C>T maps to NM_014641.2 E1772E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr6:30675514 C>T maps to NM_014641.2 Q947Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr6:30673872 G>A maps to NM_014641.2 G1029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr6:30675469 G>T maps to NM_014641.2 A962A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:41621153 G>C maps to NM_005586.3 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr6:41621213 G>T maps to NM_005586.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr7:114655787 G>A maps to NM_199072.4 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr6:37622221 G>T maps to ENST00000297153 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr6:37620081 G>A maps to ENST00000297153 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr14:47530527 C>T maps to NM_001113498.2 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr14:47315055 G>A maps to NM_001113498.2 R968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr14:47530722 G>T maps to NM_001113498.2 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr14:47504451 T>G maps to NM_001113498.2 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr2:63831867 G>A maps to NM_005917.3 K179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:207621667 C>A maps to NM_001039845.1 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr7:75684284 G>C maps to NM_005918.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:68707439 G>C maps to NM_017440.4 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:68725001 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr12:69207365 A>G maps to NM_002392.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr12:69229747 C>G maps to NM_002392.3 S275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr1:204511993 G>A maps to NM_002393.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:204501324 C>G maps to NM_002393.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr6:90402716 C>T maps to NM_014611.1 Q3344Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr6:90428325 C>T maps to NM_014611.1 W2114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr6:90362716 G>A maps to NM_014611.1 I5273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr6:90504321 G>C maps to NM_014611.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:90422325 G>A maps to NM_014611.1 N2466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr6:90402856 G>A maps to NM_014611.1 Q3298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:90420472 G>C maps to NM_014611.1 L2564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:90442462 G>A maps to NM_014611.1 F1585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr6:90421881 G>A maps to NM_014611.1 Y2508Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr6:90529308 C>A maps to NM_014611.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr6:90499949 T>C maps to NM_014611.1 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr6:90368361 C>T maps to NM_014611.1 E4996E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:90428704 C>T maps to NM_014611.1 P2034P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:90372686 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr6:90455130 C>A did not map to a codon.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr6:90438805 G>T maps to NM_014611.1 T1731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr6:90461175 T>C maps to NM_014611.1 R1067R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:83949350 T>C maps to NM_002395.4 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:48446834 G>A maps to NM_002396.4 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr6:42980213 C>T maps to NM_014623.2 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr6:42980714 C>A maps to NM_014623.2 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr3:168845828 G>T maps to NM_004991.3 C211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr3:169099219 G>A maps to NM_004991.3 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr3:168834500 G>A maps to NM_004991.3 Q387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr3:168834112 G>C maps to NM_004991.3 S516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr3:168861551 G>C maps to NM_004991.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr3:168838886 G>A maps to NM_004991.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr23:153297730 C>T did not map to a codon.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr23:153296469 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:153296575 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr23:153295961 C>A did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:29557391 C>T maps to NM_016011.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr17:37563800 G>C maps to NM_004774.3 S1558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:37564543 C>T maps to NM_004774.3 L1310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr17:37564294 G>T maps to NM_004774.3 I1393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr17:37565284 G>A maps to NM_004774.3 I1063I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:37580963 G>T maps to NM_004774.3 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr17:37576006 G>A maps to NM_004774.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:37564385 G>C maps to NM_004774.3 S1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:37576138 G>A maps to NM_004774.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr5:6378551 G>A maps to NM_032286.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:6378485 G>T maps to NM_032286.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr5:6374448 G>A maps to NM_032286.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr5:6378512 G>A maps to NM_032286.2 D28D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr23:70340863 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr23:70338700 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr23:70340914 T>G did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr23:70345220 G>T did not map to a codon.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr23:70339980 G>C did not map to a codon.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr23:70341516 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:70355031 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr23:70360616 A>G did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:70338682 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:70360538 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr23:70341527 T>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:70349951 T>C did not map to a codon.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr23:70349568 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr23:70349941 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr23:70346319 G>A did not map to a codon.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr23:70349239 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr23:70339887 G>C did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr23:70351452 C>T did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:70356466 A>G did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:70357409 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr23:70346943 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr23:70339688 T>G did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr23:70338700 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:70338694 C>G did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:70341531 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:70342960 A>G did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:70347965 G>T did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:150903166 G>T maps to NM_053002.4 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:150840607 G>A maps to NM_053002.4 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr3:150908619 C>T maps to NM_053002.4 R624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr3:151097930 C>T maps to NM_053002.4 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr3:151090535 G>A maps to NM_053002.4 L1247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr3:151112624 C>T maps to NM_053002.4 L1895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr3:150840604 A>G maps to NM_053002.4 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr17:60043856 G>C maps to NM_005121.2 L1449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr17:60023933 G>C maps to NM_005121.2 L2140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr17:60028188 A>G maps to NM_005121.2 L2096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:60059865 G>C maps to NM_005121.2 L1166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:60130027 C>A maps to NM_005121.2 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr17:60088127 G>A maps to NM_005121.2 Q584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr17:60059726 T>A maps to NM_005121.2 K1213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:60108954 G>A maps to NM_005121.2 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr17:60059761 G>T maps to NM_005121.2 S1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr17:60059865 G>T maps to NM_005121.2 L1166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr17:60033092 G>A maps to NM_005121.2 L1910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr17:60033199 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr12:116534535 G>A maps to NM_015335.4 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr12:116445437 G>A maps to NM_015335.4 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:116418743 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:116429064 G>A maps to NM_015335.4 Q1232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr12:116445260 C>T maps to NM_015335.4 K731K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr12:116446393 G>A maps to NM_015335.4 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr12:116424265 G>A maps to NM_015335.4 P1381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr12:116421304 C>T maps to NM_015335.4 L1524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:40568681 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr23:40540141 C>A did not map to a codon.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr23:40534542 G>T did not map to a codon.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr23:40571447 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:40522376 G>C did not map to a codon.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr23:40534579 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:40522376 G>A did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr22:20920797 G>A maps to NM_001003891.1 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:872057 G>T maps to NM_005481.2 R656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr19:886119 C>A maps to NM_005481.2 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:872087 G>A maps to NM_005481.2 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr19:884912 G>A maps to NM_005481.2 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr11:57472218 C>T maps to ENST00000431606 Q181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr11:57472630 G>A maps to ENST00000431606 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr12:27175536 C>T maps to NM_004264.3 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr9:136211044 G>C maps to NM_133640.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr9:136211146 G>C maps to NM_133640.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr9:136213409 G>T maps to NM_133640.3 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:131929091 G>A maps to ENST00000403834 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr6:131915383 C>T maps to ENST00000403834 A1035A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr6:131923476 G>T maps to ENST00000403834 S665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr6:131925326 C>A maps to ENST00000403834 G589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr17:38178226 G>T maps to NM_014815.3 A868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:38178926 G>C maps to NM_014815.3 L801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr17:38179629 C>T maps to NM_014815.3 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr17:38179389 C>G maps to NM_014815.3 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr17:38182547 G>A maps to NM_014815.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr19:50335587 G>C maps to NM_030973.3 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr19:50333413 C>G maps to NM_030973.3 S253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr19:16688391 G>T maps to NM_004831.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr9:134955167 G>A maps to NM_004269.2 Q22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr9:134955168 G>A maps to NM_004269.2 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:134735933 G>A maps to NM_004269.2 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr9:134738490 G>A maps to NM_004269.2 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr9:134769289 G>C maps to NM_004269.2 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:39882055 G>C maps to NM_017592.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr8:118533246 C>T maps to NM_080651.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr13:48660458 G>A maps to NM_014166.2 Q108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr17:17394773 A>T maps to NM_018019.2 K136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr15:100214789 C>T maps to ENST00000338042 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr15:100214622 C>G maps to ENST00000338042 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr15:100185845 C>T maps to ENST00000338042 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:156438786 G>A maps to NM_005920.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr1:156438614 G>A maps to NM_005920.2 Q402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:156444933 G>C maps to NM_005920.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr16:3293383 C>T maps to NM_000243.2 A701A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr16:3304194 C>T maps to NM_000243.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:3304593 C>T maps to NM_000243.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr5:126791096 G>T maps to NM_032446.2 L1010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr5:126771179 A>G maps to NM_032446.2 Q701Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr5:126705683 C>T maps to NM_032446.2 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr5:126732389 G>A maps to NM_032446.2 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr5:126781359 C>T maps to NM_032446.2 V901V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr15:66191218 C>A maps to NM_032445.2 E941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr1:3417235 G>A maps to ENST00000452816 L965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:3428642 G>A maps to ENST00000452816 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr1:3414971 G>C maps to ENST00000452816 L1180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr1:3425765 G>A maps to ENST00000452816 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr1:3424386 C>T maps to ENST00000452816 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr19:42847658 C>G maps to ENST00000251268 S515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr19:42837912 C>G maps to ENST00000251268 S115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr19:42880155 C>T maps to ENST00000251268 V2589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:42848851 C>G maps to ENST00000251268 S655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:42854307 C>T maps to ENST00000251268 S836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:42863099 G>A maps to ENST00000251268 L1779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr19:42863317 G>A maps to ENST00000251268 S1804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:42873013 G>A maps to ENST00000251268 P2167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr19:42853767 C>T maps to ENST00000251268 Q806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr19:42839191 G>A maps to ENST00000251268 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr22:42180389 C>A maps to NM_152513.3 L1045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:42139153 C>T maps to NM_152513.3 R468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr22:42126601 G>T maps to NM_152513.3 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr22:42095596 G>T maps to NM_152513.3 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr22:42191758 G>A maps to NM_152513.3 L1229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr22:42177788 C>G maps to NM_152513.3 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr10:15014540 G>A maps to NM_001080836.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:66664921 G>A maps to ENST00000407092 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:66795860 C>T maps to ENST00000407092 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr2:66664972 G>A maps to ENST00000407092 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:66665000 C>T maps to ENST00000407092 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:66665038 C>T maps to ENST00000407092 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr15:37385841 G>A maps to NM_170675.2 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr19:47920168 A>G maps to NM_020160.1 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:47910625 G>T maps to NM_020160.1 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr9:36643016 C>T maps to NM_014791.2 C286C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr9:36630324 C>G maps to NM_014791.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr2:32145936 G>C maps to NM_015955.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr11:64575137 C>T maps to NM_130804.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:64571922 C>T maps to NM_130804.2 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:64577194 G>A maps to NM_130804.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr11:64571829 G>C maps to NM_130804.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr17:41721002 C>T maps to NM_004527.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr7:15666406 G>C maps to NM_005924.4 Y218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr7:15652117 G>C maps to NM_005924.4 S270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr7:15666537 G>A maps to NM_005924.4 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr6:46803190 C>T maps to NM_005588.2 D663D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr6:46777160 G>A maps to NM_005588.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:46801037 C>T maps to NM_005588.2 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:46766859 G>A maps to NM_005588.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr6:46806750 G>T maps to NM_005588.2 E707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr6:46766362 C>T maps to NM_005588.2 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr18:29797897 C>T maps to NM_005925.2 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr18:29797899 C>A maps to NM_005925.2 S688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr18:29788196 G>A maps to NM_005925.2 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr7:100028199 C>T maps to NM_019606.5 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr7:100030606 C>T maps to NM_019606.5 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr4:88767575 C>A maps to ENST00000395102 S550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:112740455 G>A maps to NM_006343.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:112740500 G>A maps to NM_006343.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:112740536 G>C maps to NM_006343.2 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:112733014 G>A maps to NM_006343.2 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:112751898 G>A maps to NM_006343.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr15:81295005 C>T maps to NM_022566.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:81271766 G>A maps to NM_015154.1 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr15:90293763 C>T maps to NM_018670.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr15:90321348 G>C maps to NM_001039958.1 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:130138062 C>A maps to NM_002402.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr7:116436027 C>T maps to NM_001127500.1 F1359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr7:116340295 C>T maps to NM_001127500.1 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr7:116380131 G>A maps to NM_001127500.1 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr7:116398617 C>T maps to NM_001127500.1 F736F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:116435737 G>A maps to NM_001127500.1 L1294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:116339701 A>G maps to NM_001127500.1 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr7:116436173 C>G maps to NM_001127500.1 S1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr16:767323 C>T maps to NM_024042.2 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:28232682 C>G maps to NM_001113528.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr11:28232614 C>T maps to NM_001113528.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr11:62433366 C>T maps to NM_001043229.1 R6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:171765685 C>G maps to NM_015935.4 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr4:119621744 C>G maps to NM_020961.2 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr17:60526026 G>A maps to NM_181725.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr17:60525063 C>T maps to NM_181725.3 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:60501621 G>A maps to NM_181725.3 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr7:128116866 G>A maps to NM_018396.2 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr14:21969071 G>A maps to NM_019852.3 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:21971662 G>A maps to NM_019852.3 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr14:21968749 G>C maps to NM_019852.3 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr14:21971650 C>A maps to NM_019852.3 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr18:2539046 G>C maps to NM_022840.3 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:170669017 T>C maps to ENST00000442181 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:15452881 G>A maps to NM_152396.2 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr12:51318850 G>C maps to NM_014033.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr12:51319030 G>A maps to NM_014033.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr12:51319141 G>A maps to NM_014033.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:51323816 G>T maps to NM_014033.3 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr12:51318934 C>T maps to NM_014033.3 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr12:56077607 C>G maps to NM_152637.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr12:56077751 C>T maps to NM_152637.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:21629338 C>T maps to NM_016025.3 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr16:21629242 T>C maps to NM_016025.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:156051411 C>T maps to NM_001093725.1 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:156047420 C>T maps to NM_001093725.1 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:156046475 G>A maps to NM_001093725.1 C484C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:82336487 G>A maps to NM_032246.3 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr15:82336598 C>A maps to NM_032246.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:82337860 C>T maps to NM_032246.3 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr15:44102069 C>T maps to NM_005926.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr4:170913392 T>C maps to NM_021647.6 K122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr4:170913356 C>A maps to NM_021647.6 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr2:228207526 G>C maps to NM_020194.4 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr15:89449895 G>A maps to NM_005928.2 H167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr15:89449883 G>A maps to NM_005928.2 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr15:89453026 C>T maps to NM_005928.2 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr8:8750148 G>A maps to NM_004225.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr8:8749554 G>A maps to NM_004225.2 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:8750289 G>C maps to NM_004225.2 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:8749872 G>A maps to NM_004225.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr3:196753549 C>T maps to NM_005929.5 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:179083012 C>T maps to NM_033540.2 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:179080189 G>A maps to NM_033540.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:179082150 C>G maps to NM_033540.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:179096595 C>T maps to NM_033540.2 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:12061570 C>G maps to NM_014874.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:12061835 C>T maps to NM_014874.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:12056236 G>A maps to NM_014874.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr1:12062100 G>A maps to NM_014874.3 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr22:37868557 G>A maps to NM_002405.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr11:119216218 G>C maps to NM_031433.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:119217080 C>A maps to NM_031433.2 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr11:119216323 A>C maps to NM_031433.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr11:119216561 G>A maps to NM_031433.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:158520060 G>A maps to NM_022736.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr3:158537504 G>A maps to NM_022736.2 E289E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr4:2935297 G>A maps to NM_001146069.1 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr4:2934085 C>A maps to NM_001146069.1 E229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr4:2934900 G>A maps to NM_001146069.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr17:74737111 C>T maps to NM_024311.2 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr17:74737128 C>G maps to NM_024311.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr17:74774373 C>T maps to NM_024311.2 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr17:74772610 C>T maps to NM_024311.2 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:74734509 C>T maps to NM_024311.2 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:40432522 C>T maps to NM_001136493.1 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:24236210 G>A maps to ENST00000338315 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:24239768 G>A maps to ENST00000338315 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:24246001 G>A maps to ENST00000338315 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr2:24244525 C>G maps to ENST00000338315 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr2:24239105 C>T maps to ENST00000338315 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:145736433 C>T maps to NM_138431.1 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr8:145736022 C>T maps to NM_138431.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr8:145736052 C>G maps to NM_138431.1 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr8:145736007 G>T maps to NM_138431.1 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr8:145736234 C>G maps to NM_138431.1 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:205538364 C>T maps to NM_181644.4 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:205561359 C>T maps to NM_181644.4 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr1:205553192 A>G maps to NM_181644.4 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr1:205554034 G>A maps to NM_181644.4 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr1:205568335 C>T maps to NM_181644.4 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:53647276 C>T maps to NM_001170790.1 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:53647578 C>T maps to NM_001170790.1 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr12:53646948 C>T maps to NM_001170790.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr2:191301485 C>G maps to NM_017694.3 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr2:191301090 C>T maps to NM_017694.3 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:191301210 C>G maps to NM_017694.3 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:191301485 C>G maps to NM_017694.3 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:191302211 C>A maps to NM_017694.3 S486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr2:191301975 G>A maps to NM_017694.3 E407E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr17:8701571 G>T maps to NM_152599.3 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:8701946 A>C maps to NM_152599.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr17:8701868 G>A maps to NM_152599.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:8701202 C>T maps to NM_152599.3 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:682808 G>A maps to ENST00000404286 I36I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G2-A3IE-01A-11D-A20D-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-G2-AA3F-01A-12D-A42E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr4:128886261 T>C maps to NM_152778.2 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr4:128870964 G>A maps to NM_152778.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr2:103353215 C>T maps to NM_032718.3 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr2:103340297 C>A maps to NM_032718.3 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:103353178 C>A maps to NM_032718.3 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr15:41988407 C>T maps to ENST00000219905 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr15:41988905 C>T maps to ENST00000219905 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr15:42041125 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:41961766 T>G maps to ENST00000219905 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:42041073 C>T maps to ENST00000219905 R1867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr15:42028646 G>A maps to ENST00000219905 V1395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr15:42019567 A>G maps to ENST00000219905 K1207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr15:42042439 C>G maps to ENST00000219905 S2261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr15:42021427 C>T maps to ENST00000219905 R1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr15:42032369 G>C maps to ENST00000219905 L1567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr15:42054513 G>A maps to ENST00000219905 R2615R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr15:41961908 C>T maps to ENST00000219905 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr15:42003148 C>T maps to ENST00000219905 R896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr15:41988399 G>T maps to ENST00000219905 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr15:41988413 G>A maps to ENST00000219905 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:141759284 C>G maps to ENST00000475668 S1278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr7:141738408 G>C maps to ENST00000475668 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr7:141763321 C>T maps to ENST00000475668 F1427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr7:141756726 C>G maps to ENST00000475668 T1226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:141708442 G>T maps to ENST00000475668 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr7:141799459 T>C maps to ENST00000475668 P2600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr14:50089275 G>T maps to NM_002408.3 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr14:50089050 A>T maps to NM_002408.3 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr14:50088400 C>T maps to NM_002408.3 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr22:39884269 C>T maps to NM_001098270.1 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:179229051 G>A maps to NM_054013.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr5:179228874 G>A maps to NM_054013.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr5:179229065 G>A maps to NM_054013.3 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:86374017 G>A maps to ENST00000393205 H191H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr2:135180408 C>T maps to NM_002410.3 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr2:135028041 C>T maps to NM_002410.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr2:135107417 A>G maps to NM_002410.3 E385E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr2:135206324 C>T maps to NM_002410.3 F711F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr2:135170579 G>A maps to NM_002410.3 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr17:74921104 C>T maps to NM_198955.1 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr17:74921110 C>T maps to NM_198955.1 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr17:74900407 C>T maps to NM_198955.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr17:74936491 C>T maps to NM_198955.1 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:74936536 C>T maps to NM_198955.1 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr17:74936590 C>G maps to NM_198955.1 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:74902215 C>G maps to NM_198955.1 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr5:138723603 G>A maps to NM_016459.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr5:43280371 C>G maps to NM_153361.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:43246105 C>T maps to NM_153361.2 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr5:43280140 T>C maps to NM_153361.2 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr5:43280426 C>T maps to NM_153361.2 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr7:22532993 G>C maps to ENST00000441815 Y329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr7:22533266 C>T maps to ENST00000441815 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr3:127413940 C>T maps to NM_007283.5 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr12:15035936 G>A maps to NM_001190839.1 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr16:4714750 C>T maps to NM_015246.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr19:41282876 C>T maps to NM_006533.2 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr14:39717073 T>C maps to NM_054024.3 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:222805523 G>T maps to NM_198551.2 E1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr1:222825572 C>T maps to NM_198551.2 Q1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:222833628 C>T maps to NM_198551.2 R1696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr1:222801318 C>T maps to NM_198551.2 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:222827621 G>A maps to NM_198551.2 Q1453Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr18:19321720 C>T maps to NM_020774.2 N59N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr18:19345736 C>T maps to NM_020774.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr18:19378187 T>A maps to NM_020774.2 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr18:19444606 C>T maps to NM_020774.2 R1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr18:19429162 A>G maps to NM_020774.2 Q800Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr18:19321657 C>G maps to NM_020774.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:1565852 C>G maps to NM_080875.2 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:1560500 G>A maps to NM_080875.2 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:1563942 G>A maps to NM_080875.2 V796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr6:31382787 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr6:31378386 T>C maps to NM_000247.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr6:109771574 C>T maps to NM_022765.3 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:109766412 C>T maps to NM_022765.3 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:12248644 C>G maps to NM_014632.2 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr11:12247759 C>T maps to NM_014632.2 N577N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr22:18348740 G>C maps to NM_015241.2 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr22:18368658 G>A maps to NM_015241.2 I742I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr22:18364027 C>T maps to NM_001136004.1 V761V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:12341261 C>T maps to NM_032867.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr11:12315826 C>A maps to NM_032867.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr22:38327930 C>T maps to NM_033386.2 I669I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr22:38328838 C>T maps to NM_033386.2 F726F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr22:38329084 C>G maps to NM_033386.2 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:38323564 C>G maps to NM_033386.2 S538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr22:38308443 C>T maps to NM_033386.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr22:38327864 A>G maps to NM_033386.2 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr22:38323564 C>G maps to NM_033386.2 S538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr22:38328844 C>T maps to NM_033386.2 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr22:38328803 G>C did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr7:1482085 G>A maps to NM_182924.3 Q485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr7:1488388 G>A maps to NM_182924.3 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr6:31474880 C>T maps to NM_005931.3 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr6:31477643 G>C maps to NM_005931.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr6:31473464 G>T maps to NM_005931.3 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:10535149 C>T did not map to a codon.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr23:10417480 C>T did not map to a codon.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr23:10534938 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:10417653 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:10450523 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:10535263 G>T did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr23:10427829 C>G did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:10535153 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9SU-01A-31D-A391-08 chr23:10535277 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:10534930 C>T did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:107084614 G>T did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:107084504 A>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:107169433 G>C did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr23:107169340 G>A did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:107084380 T>A did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr23:107084398 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:1250393 C>T maps to NM_177401.4 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr19:1255045 C>G maps to NM_177401.4 S281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:1251878 C>T maps to NM_177401.4 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:1251887 C>T maps to NM_177401.4 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr19:1254935 C>A maps to NM_177401.4 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr19:1257171 C>T maps to NM_177401.4 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:67411831 G>T did not map to a codon.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr1:67423837 G>T maps to NM_001077700.2 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr19:307408 C>T maps to NM_017550.1 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr19:327208 C>T maps to NM_017550.1 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr5:56224635 G>A maps to ENST00000381226 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr22:24236666 G>A maps to NM_002415.1 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:73266269 C>A maps to NM_020679.2 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:12082180 C>T maps to NM_021933.2 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr1:12089840 C>G maps to NM_021933.2 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr3:97664030 G>C maps to NM_153182.2 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr3:97668764 G>C maps to NM_153182.2 S328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr17:4789240 G>A maps to NM_153827.4 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr17:4800080 C>G maps to NM_153827.4 L1296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:4789838 C>T maps to NM_153827.4 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr17:4789451 C>G maps to NM_153827.4 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr17:4797303 C>T maps to NM_153827.4 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr17:4795962 C>T maps to NM_153827.4 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr10:89265220 C>T maps to NM_004897.4 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr7:7625396 A>G maps to NM_019005.3 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:7635968 C>T maps to NM_019005.3 Q760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr7:7612384 T>C maps to NM_019005.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:7625321 G>A maps to NM_019005.3 K568K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr7:7625271 C>T maps to NM_019005.3 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr22:50927503 C>T maps to NM_017584.5 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr22:50928200 C>T maps to NM_017584.5 C258C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr12:56847524 C>A maps to NM_012064.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr13:24384057 C>G maps to NM_005932.3 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr14:37739686 C>T maps to NM_001195296.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr14:37838802 G>T maps to NM_001195296.1 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr14:37777259 G>C did not map to a codon.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr3:70014278 C>T maps to ENST00000448226 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr3:69915467 C>T maps to NM_198177.2 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:226413460 C>G maps to NM_031944.1 S216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:129905873 G>A maps to NM_002417.4 L1410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:129904352 G>A maps to NM_002417.4 I1917I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:129903221 T>G maps to NM_002417.4 G2294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:129901805 C>T maps to NM_002417.4 L2766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr10:129902318 G>A maps to NM_002417.4 D2595D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr10:129923877 G>A maps to NM_002417.4 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr10:129905046 G>C maps to NM_002417.4 S1686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr10:129903241 G>A maps to NM_002417.4 Q2288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr10:129908692 G>A maps to NM_002417.4 Q789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:129899860 C>T maps to NM_002417.4 K3122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:129914117 G>C maps to NM_002417.4 S185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr10:129899668 C>T maps to NM_002417.4 Q3186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr10:129906962 C>T maps to NM_002417.4 T1047T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr10:129904706 C>T maps to NM_002417.4 L1799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr10:129909974 G>A maps to NM_002417.4 R732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr10:129910296 C>T maps to NM_002417.4 W661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr10:129903605 C>T maps to NM_002417.4 Q2166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr10:129903923 C>T maps to NM_002417.4 E2060E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr10:129913932 C>A maps to NM_002417.4 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr10:129911689 C>T did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr2:122488510 C>T maps to NM_032390.4 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr2:122485319 G>T maps to NM_032390.4 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr22:40819590 G>A maps to NM_020831.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr22:40814491 G>A maps to NM_020831.3 I650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr7:131148048 C>T maps to NM_013255.4 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr7:131082042 G>T maps to NM_013255.4 G140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:131122753 C>T maps to NM_013255.4 Q391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:131084001 C>A maps to NM_013255.4 Y171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:47024306 C>T maps to NM_003684.4 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:2042509 C>T maps to NM_199054.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr7:140158899 C>T maps to NM_013446.3 E226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr7:140159648 G>C maps to NM_013446.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr7:140156618 C>T maps to NM_013446.3 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr3:12616307 C>T maps to NM_014160.3 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr15:23811228 C>A maps to NM_005664.3 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:28032179 G>C maps to NM_173576.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr10:28023688 G>A maps to NM_173576.2 N178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr10:28032224 G>A maps to NM_173576.2 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr10:28030297 G>A maps to NM_173576.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr22:50523211 C>T maps to NM_015166.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:50518415 C>T maps to NM_015166.3 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:50523211 C>T maps to NM_015166.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:50523235 C>T maps to NM_015166.3 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr12:121132929 C>G maps to NM_014730.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:158310241 C>T maps to NM_001195432.1 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:158289106 C>T maps to NM_022443.4 N6N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr4:185650189 C>T did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr3:37058995 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr3:37055999 C>G maps to NM_000249.3 S252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr3:37042444 G>A did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:37035094 C>T maps to NM_000249.3 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr3:37056027 C>T maps to NM_000249.3 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr3:37035094 C>T maps to NM_000249.3 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:37081764 T>C maps to NM_000249.3 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:37090078 C>T maps to NM_000249.3 F656F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr14:75514393 G>T maps to NM_001040108.1 I655I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:75513112 C>T maps to NM_001040108.1 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:75514903 C>T maps to NM_001040108.1 E485E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr14:75513241 C>T maps to NM_001040108.1 T1039T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:74716682 C>A maps to NM_152649.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr16:74729418 G>A maps to NM_152649.2 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:74706419 G>C maps to NM_152649.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr16:74726288 C>T maps to NM_152649.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr11:118344286 C>T maps to NM_001197104.1 Q805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr11:118352584 C>T maps to NM_001197104.1 R1264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr11:118376453 C>T maps to NM_001197104.1 R3283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr11:118344282 G>A maps to NM_001197104.1 L803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:118344510 G>A maps to NM_001197104.1 E879E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr11:118342390 C>T maps to NM_001197104.1 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:118369131 C>T maps to NM_001197104.1 L1950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:118390357 G>A maps to NM_001197104.1 G3724G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:118390448 G>T maps to NM_001197104.1 E3755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr11:118373659 C>T maps to NM_001197104.1 I2351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr11:118375018 C>A maps to NM_001197104.1 L2804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr11:118377245 C>T maps to NM_001197104.1 Q3547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr11:118368670 T>G maps to NM_001197104.1 Y1895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr11:118352807 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr11:118373896 G>A maps to NM_001197104.1 Q2430Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr11:118390507 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:118374636 C>G maps to NM_001197104.1 S2677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr11:118382707 C>G maps to NM_001197104.1 S3705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr11:118374379 T>A maps to NM_001197104.1 Y2591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr11:118339534 C>T maps to NM_001197104.1 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr11:118343092 C>T maps to NM_001197104.1 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:118373370 C>G maps to NM_001197104.1 S2255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:118342779 G>C maps to NM_001197104.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:118342876 G>T maps to NM_001197104.1 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr11:118344313 C>T maps to NM_001197104.1 Q814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr11:118371719 G>A maps to NM_001197104.1 W2059*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:118348835 G>T maps to NM_001197104.1 V1163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr11:118342445 C>G maps to NM_001197104.1 S191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr11:118376221 C>T maps to NM_001197104.1 S3205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:49420687 G>A maps to NM_003482.3 R5021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr12:49427646 G>T maps to NM_003482.3 S3614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr12:49428628 G>A maps to NM_003482.3 Q3441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr12:49426354 G>A maps to NM_003482.3 Q4045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr12:49436428 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr12:49436661 C>T did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:49434414 G>A maps to NM_003482.3 Q2380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:49444318 C>A maps to NM_003482.3 E1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr12:49433216 C>A did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr12:49433003 C>A did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr12:49446820 G>C maps to NM_003482.3 S330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr12:49431523 T>C maps to NM_003482.3 G3205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr12:49424158 G>A maps to NM_003482.3 Q4635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:49416551 G>A maps to NM_003482.3 Q5387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr12:49437649 C>T did not map to a codon.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr12:49440046 C>A maps to NM_003482.3 E1527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr12:49435961 C>A maps to NM_003482.3 E2007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:49445263 G>C maps to NM_003482.3 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr12:49427905 C>A maps to NM_003482.3 E3562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr12:49438594 G>C maps to NM_003482.3 S1632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr12:49424740 G>A maps to NM_003482.3 R4536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr12:49434324 G>A maps to NM_003482.3 R2410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:49434739 G>T maps to NM_003482.3 P2271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:49444683 G>A maps to NM_003482.3 Q928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:49427437 G>A maps to NM_003482.3 Q3684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:49420240 G>A maps to NM_003482.3 Q5170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:49420031 C>T maps to NM_003482.3 P5239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr12:49425448 G>A maps to NM_003482.3 Q4347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr12:49444683 G>A maps to NM_003482.3 Q928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr12:49448438 C>T maps to NM_003482.3 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr12:49420732 C>A maps to NM_003482.3 E5006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr12:49425901 G>A maps to NM_003482.3 Q4196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr12:49444667 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr12:49440083 G>T maps to NM_003482.3 Y1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr12:49427125 G>A maps to NM_003482.3 Q3788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr12:49444390 C>A maps to NM_003482.3 E994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr12:49445643 G>A maps to NM_003482.3 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr12:49447424 C>T did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr12:49445520 C>A maps to NM_003482.3 E649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:49425637 G>A maps to NM_003482.3 Q4284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr12:49448704 G>A maps to NM_003482.3 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr12:49435940 G>A maps to NM_003482.3 Q2014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr12:49446855 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr12:49444141 T>A maps to NM_003482.3 K1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr12:49420669 G>A maps to NM_003482.3 R5027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr12:49434817 G>C maps to NM_003482.3 L2245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:49445351 G>T maps to NM_003482.3 S705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr12:49433649 G>A maps to NM_003482.3 R2635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr12:49448704 G>A maps to NM_003482.3 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr12:49418469 G>A maps to NM_003482.3 Q5315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr12:49447269 G>A maps to NM_003482.3 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr12:49420163 C>T maps to NM_003482.3 Q5195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:49446361 C>A maps to NM_003482.3 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:49446374 C>G maps to NM_003482.3 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr12:49425799 G>A maps to NM_003482.3 Q4230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:49425544 G>A maps to NM_003482.3 Q4315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr12:49422946 C>A maps to NM_003482.3 G4716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr12:49425703 G>A maps to NM_003482.3 Q4262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr12:49433393 G>A maps to NM_003482.3 R2685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr12:49434306 G>A maps to NM_003482.3 Q2416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:49443509 C>T maps to NM_003482.3 E1287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr12:49444500 A>T maps to NM_003482.3 L957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr12:49446774 G>C maps to NM_003482.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr12:49431736 G>A maps to NM_003482.3 F3134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr12:49444303 G>A maps to NM_003482.3 Q1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr12:49447876 G>C maps to NM_003482.3 S186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr12:49446722 C>A maps to NM_003482.3 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr12:49444303 G>A maps to NM_003482.3 Q1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr12:49433393 G>A maps to NM_003482.3 R2685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr12:49432334 G>C maps to NM_003482.3 S2935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr12:49425097 G>A maps to NM_003482.3 Q4464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr12:49420802 C>T maps to NM_003482.3 W4982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr12:49421089 C>A maps to NM_003482.3 E4887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr12:49441750 G>A maps to NM_003482.3 S1411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:49420048 C>A maps to NM_003482.3 E5234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMJ-01A-11D-A42E-08 chr12:49446696 C>G did not map to a codon.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr12:49425037 G>A maps to NM_003482.3 R4484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr12:49419967 G>A maps to NM_003482.3 Q5261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr12:49422718 A>T maps to NM_003482.3 Y4758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr12:49421924 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr12:49423014 C>A maps to NM_003482.3 E4694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr12:49433216 C>T did not map to a codon.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr7:151879573 G>A maps to ENST00000355193 Q1791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr7:151868428 T>G did not map to a codon.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr7:151932972 C>A maps to ENST00000355193 G900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr7:151945667 T>C maps to ENST00000355193 K617K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr7:151855997 C>A maps to ENST00000355193 E3874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr7:151860061 G>A maps to ENST00000355193 Q3534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr7:151834006 G>C maps to ENST00000355193 L4939L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47W-01A-11D-A23U-08 chr7:151891117 G>A maps to ENST00000355193 Q1546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr7:151860460 T>A maps to ENST00000355193 K3401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr7:151891213 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:151859701 G>A maps to ENST00000355193 Q3654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:151904468 C>A maps to ENST00000355193 E1253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:151845579 G>A maps to ENST00000355193 R4535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:151877153 G>A maps to ENST00000355193 R2403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:151884344 A>G did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:151921148 G>A maps to ENST00000355193 R1092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr7:151900090 G>A maps to ENST00000355193 S1340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr7:151841936 G>C maps to ENST00000355193 S4792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr7:151900065 G>A maps to ENST00000355193 R1349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr7:151902228 G>C maps to ENST00000355193 S1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr7:151860302 G>A maps to ENST00000355193 F3453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr7:151845352 G>A maps to ENST00000355193 L4610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr7:151873558 G>T maps to ENST00000355193 L2993L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:151846036 C>T maps to ENST00000355193 L4382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr7:151864229 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr7:151949044 C>A maps to ENST00000355193 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:151875030 G>A maps to ENST00000355193 Q2503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr7:152132790 C>T maps to ENST00000355193 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:151879025 C>T maps to ENST00000355193 V1973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr7:151945061 G>A maps to ENST00000355193 V819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr7:151884371 G>A maps to ENST00000355193 F1661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:151874139 C>A maps to ENST00000355193 E2800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr7:151874175 G>A maps to ENST00000355193 Q2788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr7:151962240 G>A maps to ENST00000355193 Q356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr7:152009017 G>A maps to ENST00000355193 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr7:151880089 G>C maps to ENST00000355193 S1745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr7:151864286 C>A maps to ENST00000355193 E3232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr7:151949176 T>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr7:151860218 C>T maps to ENST00000355193 Q3481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr19:36220926 C>G maps to NM_014727.1 L1659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:36218435 G>C maps to NM_014727.1 L1405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:36219889 C>T maps to NM_014727.1 F1564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:36221765 C>G maps to NM_014727.1 S1812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:36210439 C>T maps to NM_014727.1 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr19:36216718 G>A maps to NM_014727.1 W1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:36211233 C>T maps to NM_014727.1 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr19:36221655 G>A maps to NM_014727.1 W1775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr19:36218513 C>G maps to NM_014727.1 L1431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:36220956 C>T maps to NM_014727.1 A1669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr19:36221295 C>T maps to NM_014727.1 F1710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:36220082 C>T maps to NM_014727.1 I1601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr7:104742502 T>G maps to NM_182931.2 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr7:104742538 T>G maps to NM_182931.2 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr7:104730617 G>A maps to NM_182931.2 Q507Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr7:104731736 G>A maps to NM_182931.2 Q566Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr7:104731754 G>A maps to NM_182931.2 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr7:104748139 C>G maps to NM_182931.2 S1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr7:104704021 A>G maps to NM_182931.2 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr7:104750986 C>G maps to NM_182931.2 S1303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:6270698 G>A maps to NM_005934.3 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr10:21823698 C>T maps to NM_004641.3 C42C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr9:20620761 G>A maps to NM_004529.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:168352585 C>T maps to ENST00000400822 L1510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr6:168272963 C>G maps to ENST00000400822 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr6:168370543 C>T maps to ENST00000400822 Q1812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr6:168352863 G>A maps to ENST00000400822 A1602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:36877000 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr17:36863215 C>T maps to NM_005937.3 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr13:49796425 G>A maps to NM_001507.1 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr2:238428647 C>A maps to NM_024101.5 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:40721522 A>C maps to ENST00000432824 *163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:40723602 G>A maps to NM_170607.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr12:122626340 G>A maps to NM_014938.3 K914K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr12:122618181 G>A maps to NM_014938.3 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr12:122614579 C>T maps to NM_014938.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr7:73008308 G>C maps to NM_032951.2 V815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr7:73038786 C>T maps to NM_032951.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr7:73008650 G>C maps to NM_032951.2 S798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr7:73020090 G>A maps to NM_032951.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr16:83948928 G>T maps to NM_012213.2 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:83933168 C>T maps to NM_012213.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:146576333 C>T maps to NM_172250.2 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr12:110002953 C>T maps to NM_052845.3 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr12:110002928 G>A maps to NM_052845.3 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr1:45974756 C>G maps to NM_015506.2 S240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr17:53491514 G>A maps to NM_012329.2 H35H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:4949653 C>A did not map to a codon.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr7:4955702 C>A maps to NM_001100600.1 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr7:4949616 T>G maps to NM_001100600.1 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:154886392 G>A maps to NM_007289.2 W631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:154861347 G>A maps to NM_007289.2 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr3:154886308 C>T maps to NM_007289.2 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr3:154864994 G>A maps to NM_007289.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr1:2523048 G>A maps to NM_033467.3 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr1:2537031 G>A maps to NM_033467.3 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr1:2529729 C>T maps to NM_033467.3 Q396Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr1:2530148 G>C maps to NM_033467.3 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:2541194 C>T maps to NM_033467.3 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:135047187 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr11:102661151 C>T maps to NM_002421.3 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr11:102642782 T>A maps to NM_002425.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr11:102645973 T>C maps to NM_002425.2 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:23306100 C>T maps to NM_004995.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr14:23306100 C>G maps to NM_004995.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr14:23312544 C>T maps to NM_004995.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMW-01A-11D-A42E-08 chr14:23312526 C>T maps to NM_004995.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr16:58077487 G>A maps to NM_002428.2 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr8:89339429 G>A maps to NM_005941.4 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr8:89128906 C>A maps to NM_005941.4 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr8:89068470 G>A maps to NM_005941.4 Q420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:132322756 C>T maps to NM_016155.4 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr12:132325333 C>T maps to NM_016155.4 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47S-01A-11D-A23U-08 chr12:56233304 A>G maps to NM_002429.4 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr12:56236138 C>A maps to NM_002429.4 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr16:55539266 C>T maps to NM_004530.4 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr16:55525776 A>G maps to NM_004530.4 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr16:55527187 C>T maps to NM_004530.4 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr16:55525728 C>G maps to NM_004530.4 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr11:102495963 G>C maps to NM_004771.3 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr11:102464204 C>T maps to NM_004771.3 Q404Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr11:102482543 C>G maps to NM_004771.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:127459065 G>A maps to NM_147191.1 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr10:127464240 G>C maps to NM_147191.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr20:33862348 C>T maps to NM_006690.3 F625F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr20:33842327 G>A maps to NM_006690.3 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr20:33834785 G>A maps to NM_006690.3 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:3107032 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:3100401 C>T maps to NM_022468.4 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:3100350 C>G maps to NM_022468.4 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr16:3108533 G>A maps to NM_022468.4 K427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr16:3107049 C>T maps to NM_022468.4 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr11:5009488 C>T maps to NM_021801.3 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr11:102576409 T>A maps to NM_022122.2 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr11:102562565 A>T maps to NM_022122.2 Y491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:102563677 G>A maps to NM_022122.2 Q430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr11:102573703 G>A maps to NM_022122.2 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:34105976 A>G maps to NM_024302.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr11:102709925 C>T maps to NM_002422.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr11:102709405 G>T maps to NM_002422.3 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:102395703 G>A maps to NM_002423.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr11:102398303 C>T maps to NM_002423.3 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr11:102586119 A>G maps to NM_002424.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr20:44640363 C>T maps to NM_004994.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr20:44640216 C>G maps to NM_004994.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr20:44640875 C>T maps to NM_004994.2 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:44642134 C>A maps to NM_004994.2 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr20:44642385 G>A maps to NM_004994.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr20:44642325 G>A maps to NM_004994.2 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr4:90816727 C>T maps to NM_007351.2 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr4:90857416 G>A maps to NM_007351.2 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr4:90857266 T>C maps to NM_007351.2 D812D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:88696505 C>T maps to NM_024756.2 K948K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:88704121 G>A maps to NM_024756.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr22:28193513 C>T maps to NM_002430.2 T1006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:61285475 C>T maps to NM_002431.3 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr1:158815538 C>T maps to NM_002432.1 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr1:158812189 C>T maps to NM_002432.1 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr1:158813153 C>T maps to NM_002432.1 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:93649974 G>A maps to NM_022151.4 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr14:93650481 C>A maps to NM_022151.4 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr11:1491479 G>A maps to NM_001172223.1 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr4:71847760 C>G maps to ENST00000396051 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr4:71824734 C>T maps to ENST00000396051 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr2:74394142 C>T maps to NM_018221.3 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr9:27455340 G>T maps to NM_024761.3 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr1:47078822 G>A maps to NM_145279.4 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:198380839 G>A maps to NM_015387.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr18:33785187 C>T maps to NM_017947.2 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr18:33767630 C>T maps to NM_017947.2 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr18:33831207 C>G maps to NM_017947.2 S709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr18:33785223 C>T maps to NM_017947.2 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:39895071 G>A maps to ENST00000425303 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr6:39895179 C>T maps to ENST00000425303 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr6:39895170 G>A maps to ENST00000425303 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr20:49575531 G>A maps to NM_014484.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr20:49576559 G>A maps to NM_014484.3 W394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr20:49576334 C>A maps to NM_014484.3 S319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr20:49575822 C>G maps to NM_014484.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:49576221 G>C maps to NM_014484.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:49575456 G>A maps to NM_014484.3 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:49575978 C>T maps to NM_014484.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:49576167 C>A maps to NM_014484.3 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:49576536 G>A maps to NM_014484.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:75439096 G>A maps to NM_025098.2 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr11:75439858 C>A maps to NM_025098.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr11:75439963 C>G maps to NM_025098.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr7:100839277 C>T maps to NM_178176.2 E325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr2:74691733 G>A maps to NM_006302.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:74689844 C>T maps to NM_006302.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr2:74689267 G>A maps to NM_006302.2 Q550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:74688923 C>T maps to NM_006302.2 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr3:49947847 G>A maps to NM_032355.3 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr16:77232006 G>A maps to NM_014940.2 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr16:77232203 G>A maps to NM_014940.2 *548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr16:77229557 G>A maps to NM_014940.2 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:62861091 C>T maps to ENST00000393630 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:62931483 C>T maps to ENST00000393630 Q706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:108724085 G>C maps to NM_014429.3 S615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr3:108719424 C>T maps to NM_014429.3 T722T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr3:108698498 C>G maps to NM_014429.3 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr22:31337499 A>G maps to ENST00000397641 Y248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr21:37747542 T>C maps to ENST00000290384 D924D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr21:37717292 C>T maps to ENST00000290384 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:106219838 C>T did not map to a codon.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr23:106186425 T>C did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr23:106221415 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr23:106243185 C>T did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:106224143 C>T did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:106186172 T>C did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:106185962 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr23:106186369 G>C did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr15:79178555 C>T maps to NM_206839.1 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr23:102931202 T>C did not map to a codon.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr23:102931421 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:2268253 G>A maps to NM_024848.1 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr9:124936901 C>T maps to NM_198469.2 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr8:57026487 C>T maps to NM_005372.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:220970026 C>T maps to NM_022746.3 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:220964943 C>T maps to NM_022746.3 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr1:220935150 C>T maps to NM_017898.3 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr1:220928390 C>T maps to NM_017898.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr1:220936277 C>G maps to NM_017898.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr1:220928420 G>A maps to NM_017898.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr23:14910876 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:14937847 A>T did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr23:14937912 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr23:14891875 G>T did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr23:14932632 A>C did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:100212804 G>A maps to NM_023948.4 *236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:113234325 G>T maps to NM_020963.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:113232207 C>G maps to NM_020963.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr22:50563823 C>T maps to NM_018995.2 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:50591559 C>A maps to NM_018995.2 V993V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr22:50580508 G>A did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr22:50530601 G>C maps to NM_018995.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:132643946 C>G maps to NM_015529.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr17:7490057 C>T maps to NM_004870.3 C117C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-GV-A6ZA-01A-12D-A339-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr9:13168546 A>G maps to ENST00000319217 A1024A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr9:13221382 T>G maps to ENST00000319217 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:13224525 G>A maps to ENST00000319217 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr11:58979999 G>C maps to NM_001039396.1 Y113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:58978820 G>C maps to NM_001039396.1 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr11:58978634 G>A maps to NM_001039396.1 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr11:58979535 G>C maps to NM_001039396.1 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr11:58979861 G>C maps to NM_001039396.1 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr16:82203771 G>A maps to NM_005792.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr16:82183008 C>A did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:20220722 G>A maps to ENST00000414242 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr13:20240701 G>A maps to ENST00000414242 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr12:123641395 C>T maps to NM_022782.2 T1018T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:123645930 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr15:75185570 C>T maps to NM_002435.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr15:75183865 C>T maps to NM_002435.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr15:75189513 C>G maps to NM_002435.1 S336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr15:75189911 G>A maps to NM_002435.1 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr15:75190014 C>T maps to NM_002435.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:43805110 G>A maps to NM_005373.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr1:43804267 C>T maps to NM_005373.2 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:43805638 C>G maps to NM_005373.2 S232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:43805738 C>T maps to NM_005373.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr19:4352928 G>C maps to ENST00000262967 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:4359176 C>T maps to ENST00000262967 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr19:4357560 C>T maps to ENST00000262967 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr19:4359210 G>T maps to ENST00000262967 E460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:56349050 G>A maps to ENST00000340482 I697I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:56350925 G>A maps to ENST00000340482 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr17:56358092 G>A maps to ENST00000340482 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:56356967 G>C maps to ENST00000340482 S155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr23:154010077 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr23:154014675 C>G did not map to a codon.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr17:41960381 G>C maps to NM_005374.3 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr17:41958143 C>G maps to NM_005374.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr17:41958909 G>A maps to NM_005374.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:41907105 G>A maps to ENST00000398393 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr17:41879197 C>T maps to ENST00000398393 R568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr17:41901304 C>T maps to ENST00000398393 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr17:41907060 C>G maps to ENST00000398393 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr14:67779321 C>T maps to NM_022474.2 Q374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr7:24708259 A>G maps to ENST00000409253 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr10:28358781 C>A did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr10:28348589 T>C maps to NM_173496.3 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr10:28420611 G>A maps to NM_173496.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr18:11886743 G>A maps to ENST00000344987 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr18:11886993 G>A maps to ENST00000344987 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr18:11884521 G>A maps to ENST00000344987 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr22:43870628 C>T maps to NM_001044370.1 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr22:43870640 C>T maps to NM_001044370.1 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr22:43821053 C>T maps to NM_001044370.1 C21C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr22:43821216 T>C did not map to a codon.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr11:30439146 T>C maps to NM_001584.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr17:17083383 C>T maps to NM_015134.2 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr17:17080691 G>A maps to NM_015134.2 E975E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr17:17080712 G>A maps to NM_015134.2 T982T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:17080619 G>A maps to NM_015134.2 A951A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr17:17080664 C>G maps to NM_015134.2 L966L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr17:17083937 C>G maps to NM_201274.2 V1021V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr22:37425329 G>A maps to NM_021126.4 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr22:37425359 C>T maps to NM_021126.4 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:18304801 C>T maps to NM_032683.2 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:161276524 G>A maps to ENST00000360451 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:161276625 C>T maps to ENST00000360451 W117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:167741608 C>A maps to NM_003953.5 S119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr1:167741687 C>T maps to NM_003953.5 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr11:118104204 C>T maps to NM_198275.1 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:181018368 G>A maps to NM_001531.2 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:181019243 G>C maps to NM_001531.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:181003154 G>A maps to NM_001531.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr3:138121044 G>A maps to NM_001085049.1 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:18112245 C>G maps to NM_002438.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr10:18122664 G>A maps to NM_002438.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:60767310 G>A maps to NM_006039.3 Q1210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:60749514 T>C did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:60743623 C>T maps to NM_006039.3 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:60744208 C>T maps to NM_006039.3 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr11:94194100 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr11:94197306 G>A maps to NM_005591.3 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr4:6642606 C>T maps to NM_033296.1 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr4:6642856 G>T maps to NM_033296.1 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr4:6711005 G>A maps to NM_203462.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr4:6711275 G>A maps to NM_203462.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:6711005 G>C maps to NM_203462.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:68747723 G>A maps to NM_198923.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:68748224 G>A maps to NM_198923.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:68748292 G>A maps to NM_198923.2 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:68748395 C>G maps to NM_198923.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr11:68748292 G>A maps to NM_198923.2 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr11:68748143 C>T maps to NM_198923.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr11:3249612 C>T maps to ENST00000328215 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr11:3249789 G>A maps to ENST00000328215 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:68773666 C>T maps to NM_145015.4 Q37Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr11:68773591 G>A maps to NM_145015.4 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:18956184 G>T maps to NM_147199.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr11:18955395 G>A maps to NM_147199.3 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr11:19077061 G>A maps to NM_054030.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr11:18159609 G>A maps to NM_054031.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr11:18195534 G>T maps to NM_054032.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr11:18195141 G>A maps to NM_054032.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr11:18194979 C>T maps to NM_054032.3 N59N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr19:13882983 C>T maps to NM_001031727.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:13875419 C>T maps to NM_001031727.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:13882932 A>G did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:34964209 C>T maps to NM_024864.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:21751240 C>T maps to NM_024026.4 H62H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr13:21751153 G>A maps to NM_024026.4 Q33Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr4:78806486 T>C maps to NM_020236.3 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:45904543 G>A maps to NM_145255.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr17:45901690 G>C maps to NM_145255.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr17:45901603 C>T maps to NM_145255.3 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr17:79674000 G>A maps to NM_002949.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr17:79673991 G>C maps to NM_002949.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr6:44081612 G>A maps to NM_032111.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr8:55049830 C>T maps to NM_014175.3 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr11:6704518 C>T maps to NM_022061.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:1342309 C>T maps to NM_017971.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:1337498 A>G maps to NM_017971.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:1342522 C>T maps to NM_017971.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr5:154346441 C>T maps to NM_014180.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr5:154346276 G>A maps to NM_014180.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr11:1973374 C>T maps to NM_021134.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr11:1977517 G>A maps to NM_021134.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr11:1972203 C>T maps to NM_021134.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:48445521 G>C maps to NM_016504.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr16:417714 G>C maps to NM_006428.4 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr3:131220432 T>C maps to ENST00000425847 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr7:42974728 A>G maps to NM_031903.2 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:27997347 G>A maps to NM_004891.3 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:86437694 C>T maps to NM_016622.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr2:86437694 C>T maps to NM_016622.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:54675718 G>A maps to NM_016491.3 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:54670970 G>A maps to NM_016491.3 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr1:54670817 C>T maps to NM_016491.3 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr1:54670832 C>A maps to NM_016491.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr17:73898164 C>T maps to NM_032478.3 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr17:73897804 C>T maps to NM_032478.3 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr21:26978899 G>C maps to NM_080794.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr21:26966215 G>C maps to NM_080794.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:10369341 C>T maps to NM_146387.1 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr19:10363230 C>G maps to NM_146387.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr22:19422282 G>A maps to NM_003776.2 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr22:19423379 G>A maps to NM_003776.2 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:140446922 C>T maps to NM_032477.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:140446844 C>T maps to NM_032477.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr9:140446838 G>A maps to NM_032477.2 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr9:140446763 C>G maps to NM_032477.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr10:102741295 G>A maps to NM_176794.1 I220I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-XF-A9ST-01A-11D-A42E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr17:36476626 C>T maps to NM_032351.3 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:179306755 G>A maps to NM_020409.2 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr3:179306766 G>A maps to NM_020409.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:104153097 C>A maps to NM_019051.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:6602076 C>T maps to NM_016497.3 W47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr14:23299419 C>T maps to NM_178336.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:74699246 C>A maps to NM_053050.3 *113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:74699246 C>T maps to NM_053050.3 *113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:151733962 C>T maps to NM_031420.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr6:42176088 C>A maps to NM_018141.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr19:39422994 C>G maps to NM_033363.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:174987625 G>T maps to NM_022100.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr1:174987586 G>C maps to NM_022100.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr10:75011599 G>C maps to NM_016065.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr10:75011599 G>A maps to NM_016065.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr7:56022648 G>A maps to ENST00000426595 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr7:56022675 C>T maps to ENST00000426595 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:43655471 G>A maps to ENST00000372118 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:138395831 C>G maps to NM_016034.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:150280532 T>C maps to NM_031901.4 Y45Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:150280533 G>T maps to NM_031901.4 E46*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-E7-A7PW-01A-11D-A34U-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-MV-A51V-01A-11D-A26M-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-GV-A3JZ-01A-11D-A21A-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-GV-A3JZ-01A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr20:3027132 C>T maps to NM_030811.3 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr8:80942414 G>A maps to NM_014018.2 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr13:41345135 G>T maps to NM_005830.3 S46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr13:41340883 C>T maps to NM_005830.3 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr16:1822221 C>T maps to ENST00000432952 *226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr2:95766233 T>A maps to NM_031902.3 K306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr21:35497669 G>A maps to NM_032476.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr17:73261874 G>A maps to NM_015971.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:125042728 G>C maps to NM_138777.3 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:19584360 C>T maps to NM_016183.3 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:19585254 G>A maps to NM_016183.3 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr1:19582479 C>T maps to NM_016183.3 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr11:10622525 C>T maps to NM_001098579.1 A643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr11:10602123 A>G maps to NM_001098579.1 G782G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:60184147 G>A maps to NM_032597.3 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr11:60184401 G>A maps to NM_032597.3 W654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr11:60183916 C>A maps to NM_032597.3 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:59863128 A>C maps to NM_000139.4 *245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr11:59828762 C>T maps to NM_006138.4 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr11:59828719 G>C maps to NM_006138.4 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:59828764 G>A maps to NM_006138.4 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr11:60070102 T>C maps to NM_148975.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:60070048 A>G maps to NM_148975.1 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:60048184 G>T maps to NM_148975.1 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr11:59939726 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:60154218 C>T maps to NM_206939.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr11:60468497 G>A maps to NM_031457.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr8:72755903 G>A maps to NM_005098.3 N170N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr2:47705482 G>T maps to NM_000251.1 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:47641446 G>T maps to NM_000251.1 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr2:47703707 C>G maps to NM_000251.1 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:47703557 A>T maps to NM_000251.1 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:47639621 C>T maps to NM_000251.1 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:47709967 C>G maps to NM_000251.1 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:79950602 G>A maps to NM_002439.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:79970868 C>T maps to NM_002439.3 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr5:79974806 C>G maps to NM_002439.3 S412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr5:79965994 C>A maps to NM_002439.3 S220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr5:79950578 C>T maps to NM_002439.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr5:79950578 C>G maps to NM_002439.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr5:80109518 A>G maps to NM_002439.3 A924A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr1:76262800 C>A maps to NM_002440.2 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr1:76262725 C>A maps to NM_002440.2 S19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:76262774 C>G maps to NM_002440.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:31710891 G>A maps to ENST00000375742 Q120Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr6:31712334 G>A maps to ENST00000375742 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr6:31729659 G>A maps to ENST00000375742 A766A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr6:31711795 C>T maps to ENST00000375742 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:31711762 C>G maps to ENST00000375742 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr2:48027213 C>T maps to NM_000179.2 Q698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr2:48026078 G>A maps to NM_000179.2 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:48018161 C>T maps to NM_000179.2 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr2:48032802 C>G maps to NM_000179.2 L1201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr17:55335714 G>A maps to NM_138962.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:135870900 G>A maps to NM_018133.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr23:11783847 A>G did not map to a codon.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr23:11786763 C>T did not map to a codon.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr23:11780320 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr23:11783729 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:11783670 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr23:11781933 G>A did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:11783734 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:234774884 G>T did not map to a codon.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr2:234775807 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr2:234775295 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr16:816938 C>G maps to NM_013404.4 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr16:820212 G>A maps to NM_001025190.1 T924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr16:830826 G>A maps to NM_001025190.1 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr16:830499 G>A maps to NM_001025190.1 H167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr16:824484 G>A maps to NM_001025190.1 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr9:35754039 G>C maps to NM_001044264.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:64957100 C>T did not map to a codon.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr23:64949311 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr23:64959691 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:64959736 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:16026068 G>T maps to ENST00000445506 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr10:23408305 G>T maps to ENST00000277598 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:23408325 G>A maps to ENST00000277598 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr10:23399190 G>T maps to ENST00000277598 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr10:23399244 C>T maps to ENST00000277598 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:65857023 A>G maps to NM_001031679.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr3:49721755 C>T maps to NM_020998.3 G669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:49725031 C>T maps to NM_020998.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr3:49721549 G>T maps to NM_020998.3 R697R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr3:49721499 C>T maps to NM_020998.3 V713V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:49723779 G>A maps to NM_020998.3 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr3:49723040 G>A maps to NM_020998.3 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr3:49723876 G>A maps to NM_020998.3 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:49933756 C>T maps to NM_002447.2 G840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr3:49929004 C>A maps to NM_002447.2 E1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr3:49932964 C>G maps to NM_002447.2 L993L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr3:49940130 T>C maps to NM_002447.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr3:49941017 G>A maps to NM_002447.2 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr3:49928678 G>A maps to NM_002447.2 L1199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr3:49928718 G>A maps to NM_002447.2 L1185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr3:49929254 G>A maps to NM_002447.2 V1096V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr3:49935087 C>T maps to NM_002447.2 E637E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr3:49932627 G>A maps to NM_002447.2 V1081V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr3:49927493 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr3:49933756 C>T maps to NM_002447.2 G840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:49936678 G>A maps to NM_002447.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr3:49940148 G>A maps to NM_002447.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr23:131188742 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:190925045 G>A maps to NM_005259.2 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr2:190927241 A>G maps to NM_005259.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:155582216 G>A maps to NM_018116.2 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr16:56672670 C>T maps to NM_005946.2 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr14:105936421 C>A maps to NM_004689.3 S673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr2:42836605 G>T maps to ENST00000405094 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr9:21854823 C>T maps to NM_002451.3 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:121514759 A>G maps to NM_022045.3 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr8:121468866 C>A maps to NM_022045.3 S235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr8:121535569 G>A maps to NM_022045.3 K903K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr6:36946337 C>T maps to ENST00000373627 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:47660528 G>C maps to NM_014342.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:47644271 C>T maps to NM_014342.3 W269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr11:47663975 G>A maps to NM_014342.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:154294195 C>A did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr23:154292252 T>G did not map to a codon.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr8:98718937 C>A maps to NM_178812.3 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr8:98718972 C>T maps to NM_178812.3 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:91503795 C>T maps to NM_006980.3 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:91503774 A>T maps to NM_006980.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr8:97256295 C>A maps to NM_015942.3 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr8:97256206 C>A maps to NM_015942.3 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr12:107372069 A>G maps to NM_025198.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:38289445 G>T maps to NM_005955.2 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr1:93584937 C>G maps to NM_007358.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:93575838 C>T maps to NM_007358.3 R20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:93602499 A>G maps to NM_007358.3 E566E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr15:65316098 C>T maps to NM_139242.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:66619458 G>A maps to NM_014637.3 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr8:66617031 C>T maps to NM_014637.3 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr10:135213088 C>A maps to NM_138384.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:135213088 C>T maps to NM_138384.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr14:64894141 C>T maps to NM_005956.3 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr14:64921556 C>T maps to NM_005956.3 S894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr14:64877851 G>T maps to NM_005956.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr6:151243415 C>T maps to NM_015440.3 Q354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr6:151203954 C>T maps to NM_015440.3 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr6:151197291 G>A maps to NM_015440.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr2:74432978 C>G maps to NM_006636.3 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr2:74432987 C>T maps to NM_006636.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr1:11854537 C>G maps to ENST00000376585 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:11852390 G>A maps to ENST00000376585 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr1:11854050 G>A maps to ENST00000376585 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:55481207 T>G maps to NM_002453.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:149809882 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:149807436 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:149809877 G>A did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:149809840 G>T did not map to a codon.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr23:149826365 A>G did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:149783102 G>A did not map to a codon.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr23:149818251 A>G did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr23:149767124 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr23:149807417 A>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:149867720 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr23:149895704 T>A did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr23:149905821 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr23:149867759 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr23:149900043 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:149895710 C>A did not map to a codon.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr23:149931145 T>C did not map to a codon.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr23:149901028 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:31269111 T>C maps to NM_017762.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:149906109 G>A maps to NM_001145862.1 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr1:149908107 A>G maps to NM_001145862.1 N27N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr1:149906157 C>T maps to NM_001145862.1 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:149901050 G>A maps to NM_001145862.1 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:32233925 C>A maps to NM_001040446.1 E543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr5:32230021 G>C maps to NM_001040446.1 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr5:32229904 G>A maps to NM_001040446.1 F741F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr5:32230144 C>T maps to NM_001040446.1 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:32239279 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:31197388 G>T maps to NM_014967.4 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr15:31210495 G>A maps to NM_014967.4 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr11:95595479 G>A maps to NM_016156.5 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr22:30415618 A>G maps to NM_021090.3 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr22:30387503 C>G maps to NM_021090.3 S102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:56569024 C>T maps to NM_004687.4 *1196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr17:56581514 G>A maps to NM_004687.4 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr17:56570242 G>T maps to NM_004687.4 S1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr17:56584221 C>T maps to NM_004687.4 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr17:56569116 G>C maps to NM_004687.4 V1165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr17:56586078 C>G maps to NM_004687.4 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr17:56572878 A>T maps to NM_004687.4 L875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:25823573 T>C maps to NM_004685.3 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr13:25826112 C>T maps to NM_004685.3 E452E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr13:25828052 G>A maps to NM_004685.3 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr8:17169028 C>T maps to NM_004686.4 K364K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr23:63488417 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:63488549 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:63488785 C>G did not map to a codon.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr23:63568656 A>G did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr23:63548759 G>A did not map to a codon.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr8:11172555 G>T maps to NM_015458.3 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr4:187455003 G>A maps to NM_005958.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr11:92715325 C>T maps to NM_005959.3 Q313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr11:92715237 C>G maps to NM_005959.3 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr11:92703068 C>T maps to NM_005959.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr6:74191779 C>T maps to NM_001123226.1 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr6:74171786 C>T maps to NM_001123226.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr1:11270888 G>A maps to NM_004958.3 L1212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:11308145 C>G maps to NM_004958.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr1:11288889 C>G maps to NM_004958.3 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:11269464 C>T maps to NM_004958.3 R1235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr1:11186834 G>A maps to NM_004958.3 Q2124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:11194508 C>T maps to NM_004958.3 Q1715Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:30824561 C>T maps to NM_001003704.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr10:30638053 C>A maps to NM_018109.3 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr10:30625884 G>A maps to ENST00000358107 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr7:135635364 C>T maps to NM_145808.3 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr1:236979840 C>T maps to NM_000254.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr1:237060353 C>G maps to NM_000254.2 S1216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:237054613 T>C maps to NM_000254.2 Y1063Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr1:237049647 G>A maps to NM_000254.2 W944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:237024568 C>T maps to NM_000254.2 L730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr13:41834629 T>C maps to NM_004294.2 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr6:153316426 C>A maps to NM_019041.5 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:153323591 C>A maps to NM_019041.5 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr5:7895908 C>T maps to NM_024010.2 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr5:7895917 G>T maps to NM_024010.2 V570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr8:125568499 C>T maps to NM_014751.4 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr8:125579321 G>C maps to NM_014751.4 S239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr8:125580652 G>A maps to NM_014751.4 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr8:125580730 G>C maps to NM_014751.4 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr8:125601933 C>G maps to NM_014751.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr16:70713226 C>G did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr16:70713607 C>G did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr16:70711733 C>T maps to NM_138383.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr16:70698044 C>T maps to NM_138383.2 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr4:100542244 C>T maps to ENST00000511045 I817I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr4:100532320 G>C maps to ENST00000511045 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr4:100510815 C>G maps to ENST00000511045 S164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:100512944 G>A maps to ENST00000511045 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr4:100503107 C>G maps to ENST00000511045 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr4:100503107 C>G maps to ENST00000511045 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr4:100518249 G>A maps to ENST00000511045 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr4:100521886 C>G maps to ENST00000511045 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr4:100518240 G>A maps to ENST00000511045 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr8:17507471 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr8:17611486 C>T maps to NM_001001924.2 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr13:29599704 G>C maps to NM_001033602.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr13:29599350 G>A maps to NM_001033602.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr13:29599200 G>A maps to NM_001033602.2 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr13:29599291 G>T maps to NM_001033602.2 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr13:29599308 T>C maps to NM_001033602.2 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr13:29599890 A>G maps to NM_001033602.2 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr13:29600797 C>T maps to NM_001033602.2 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr2:177161615 A>G maps to NM_006554.4 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr5:79279589 G>A maps to ENST00000512528 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr5:79279554 C>T maps to ENST00000512528 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr1:155160659 C>T maps to ENST00000425082 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:155160208 G>C maps to ENST00000425082 S443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr3:124646826 T>C maps to NM_033049.3 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:124641133 C>T maps to NM_033049.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr3:124646787 C>G maps to NM_033049.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr11:26587102 T>C maps to NM_001135091.1 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr11:26587345 C>T maps to NM_001135091.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:26584756 G>C maps to NM_001135091.1 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr11:26587353 G>A maps to NM_001135091.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr19:8993546 T>C did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:8999055 G>A maps to NM_024690.2 F13596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr19:9085812 G>C maps to NM_024690.2 S2001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr19:9065494 G>A maps to NM_024690.2 I7317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr19:9025598 G>A maps to NM_024690.2 T12285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr19:9057195 G>A maps to NM_024690.2 L10084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr19:9009268 G>C maps to NM_024690.2 L13068L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr19:9009297 G>A maps to NM_024690.2 L13059L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:9077703 G>A maps to NM_024690.2 Q3248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:9067795 C>T maps to NM_024690.2 V6550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:9091499 C>T maps to NM_024690.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr19:9061675 C>T maps to NM_024690.2 V8590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:9001861 C>G maps to NM_024690.2 S13462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:9082527 G>T maps to NM_024690.2 S3096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:9025597 A>G maps to NM_024690.2 L12286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:9059941 G>A maps to NM_024690.2 H9168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:9045729 G>T maps to NM_024690.2 I11967I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:9058479 C>A maps to NM_024690.2 E9656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:9068833 G>T maps to NM_024690.2 L6204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:9070753 G>A maps to NM_024690.2 T5564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:9076713 C>A maps to NM_024690.2 E3578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:9083744 C>T maps to NM_024690.2 E2690E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B0-01A-11D-A31L-08 chr19:9072517 G>A maps to NM_024690.2 T4976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr19:9058016 G>C maps to NM_024690.2 S9810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr19:9011340 C>T maps to NM_024690.2 R12964R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr19:9048544 G>T maps to NM_024690.2 S11029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr19:9070990 C>T maps to NM_024690.2 L5485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr19:9084266 G>T maps to NM_024690.2 A2516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr19:9017492 C>A maps to NM_024690.2 G12611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr19:9070617 G>T maps to NM_024690.2 R5610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr19:8993376 G>C maps to NM_024690.2 V13904V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr19:8971699 G>A maps to NM_024690.2 Q14298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:9086460 G>T maps to NM_024690.2 S1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:9088658 C>T maps to NM_024690.2 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr19:9070792 G>A maps to NM_024690.2 L5551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr19:9087677 C>T maps to NM_024690.2 P1379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr19:9070120 T>C maps to NM_024690.2 E5775E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr19:9016708 G>T maps to NM_024690.2 S12676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr19:9058630 G>T maps to NM_024690.2 Y9605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:9001858 T>C maps to NM_024690.2 R13463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:9090785 G>C maps to NM_024690.2 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:8969427 C>G did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:9083459 C>G maps to NM_024690.2 V2785V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr19:9076789 A>T maps to NM_024690.2 T3552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr19:9069356 G>C maps to NM_024690.2 S6030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr19:9075646 G>A maps to NM_024690.2 A3933A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr19:9074152 G>T maps to NM_024690.2 L4431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr19:9070792 G>C maps to NM_024690.2 L5551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:9086870 G>T maps to NM_024690.2 A1648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr19:9069855 G>A maps to NM_024690.2 Q5864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:9000462 C>T maps to NM_024690.2 T13507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr19:9061279 T>G maps to NM_024690.2 A8722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr19:9065701 C>T maps to NM_024690.2 L7248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr19:9002510 G>C maps to NM_024690.2 L13435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr19:9019598 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr19:9066444 G>A maps to NM_024690.2 Q7001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr19:9086273 G>A maps to NM_024690.2 L1847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:9062137 G>C maps to NM_024690.2 V8436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:9071114 G>C maps to NM_024690.2 S5444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr19:9076876 C>T maps to NM_024690.2 A3523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:9082832 A>G maps to NM_024690.2 Y2994Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr19:9047957 G>A maps to NM_024690.2 L11225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr19:9015691 T>A maps to NM_024690.2 K12711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:9064402 C>T maps to NM_024690.2 V7681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr19:9089751 G>C maps to NM_024690.2 S688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr19:9049261 G>C maps to NM_024690.2 S10790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr19:9057643 G>T maps to NM_024690.2 I9934I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:9065726 G>C maps to NM_024690.2 S7240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr19:9007505 G>A maps to NM_024690.2 S13154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr19:9059417 G>C maps to NM_024690.2 S9343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr19:8994152 C>T maps to NM_024690.2 L13844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:9049769 C>A maps to NM_024690.2 E10621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:9089780 G>C maps to NM_024690.2 V678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr7:100679487 T>C maps to NM_001040105.1 P1597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr7:100687056 G>A maps to NM_001040105.1 K4120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr7:100692213 C>T maps to NM_001040105.1 S4208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:100695123 C>T maps to NM_001040105.1 F4328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:100696365 G>A maps to NM_001040105.1 L4401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:100684882 G>T maps to NM_001040105.1 E3396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:100679289 C>A maps to NM_001040105.1 I1531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr7:100679550 T>C maps to NM_001040105.1 G1618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr7:100685856 C>G maps to NM_001040105.1 V3720V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr7:100683864 G>C maps to NM_001040105.1 T3056T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr7:100677276 T>C maps to NM_001040105.1 Y860Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr7:100680144 C>T maps to NM_001040105.1 S1816S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr7:100678977 G>A maps to NM_001040105.1 G1427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr7:100684455 G>A maps to NM_001040105.1 L3253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr7:100684166 C>G maps to NM_001040105.1 S3157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr7:100685840 C>G maps to NM_001040105.1 S3715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr7:100679216 C>G maps to NM_001040105.1 S1507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr7:100675542 C>A maps to NM_001040105.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr7:100675896 C>G maps to NM_001040105.1 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr7:100676733 A>T maps to NM_001040105.1 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr7:100683690 G>A maps to NM_001040105.1 P2998P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr7:100678842 A>G maps to NM_001040105.1 E1382E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:100677231 A>G maps to NM_001040105.1 S845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr7:100695084 G>A maps to NM_001040105.1 E4315E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr7:100679223 T>C maps to NM_001040105.1 P1509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr7:100676915 C>G maps to NM_001040105.1 S740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr11:1093739 G>C maps to ENST00000441003 P1853P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr11:1102478 C>T maps to ENST00000441003 P2621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr11:1099442 C>T maps to ENST00000441003 V2428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:1081799 G>A maps to ENST00000441003 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr11:1084793 C>T maps to ENST00000441003 Y863Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr11:1101651 C>T maps to ENST00000441003 F2555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:1097900 C>T maps to ENST00000441003 Q2332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr11:1093787 C>G maps to ENST00000441003 L1869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr11:1078357 C>T maps to ENST00000441003 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:195452034 C>T maps to ENST00000447234 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr3:195453357 C>T maps to ENST00000447234 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr3:195453216 C>G maps to ENST00000447234 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:195456585 A>G maps to ENST00000447234 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr3:195452814 G>A maps to ENST00000447234 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr3:195479243 C>T maps to NM_018406.5 S5194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr3:195477928 C>T maps to NM_018406.5 S5234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr3:195501045 G>C maps to NM_018406.5 L4358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr3:195480081 C>G maps to NM_018406.5 L5116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr3:195492179 G>A maps to NM_018406.5 Q4587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr3:195497089 G>A maps to NM_018406.5 L4465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr3:195480014 G>A maps to NM_018406.5 L5139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr11:1251360 C>G maps to ENST00000447027 Y452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:1272546 C>T maps to ENST00000447027 L4816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr11:1257644 C>A maps to ENST00000447027 T973T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr11:1273631 C>T maps to ENST00000447027 Q4978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr11:1261065 C>T maps to ENST00000447027 F1210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr11:1279389 C>A maps to ENST00000447027 I5507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr11:1272041 G>A maps to ENST00000447027 G4647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:1268536 C>A maps to ENST00000447027 S3479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr11:1267502 G>A maps to ENST00000447027 T3134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr11:1262876 C>T maps to ENST00000447027 Y1592Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:1263618 G>T maps to ENST00000447027 E1840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr11:1267769 C>T maps to ENST00000447027 T3223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:1274061 G>A maps to ENST00000447027 E5026E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr11:1272701 G>A maps to ENST00000447027 T4867T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:1271639 G>T maps to ENST00000447027 L4513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr11:1025205 G>C maps to NM_005961.2 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr11:1026379 G>A maps to NM_005961.2 F831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:1025892 G>C maps to NM_005961.2 S904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr11:1028661 G>A maps to NM_005961.2 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr11:1017907 G>A maps to NM_005961.2 V1631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr11:1018414 G>A maps to NM_005961.2 V1462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr11:1018561 C>A maps to NM_005961.2 G1413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr11:1018723 C>T maps to NM_005961.2 T1359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr11:1017271 G>A maps to NM_005961.2 F1843F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:71339776 G>A maps to NM_152291.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:20827203 C>T maps to NM_024544.2 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr1:20827461 C>G maps to NM_024544.2 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:1356433 T>C maps to NM_032853.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr19:1376573 G>C maps to NM_032853.3 *712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr19:1376551 G>T maps to NM_032853.3 E705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr23:105450562 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:105450251 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr23:105449659 C>G did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr9:103348231 C>T maps to NM_001018116.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr9:103340781 C>G maps to NM_001018116.1 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr9:113547875 C>T maps to ENST00000189978 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:113562940 C>T maps to ENST00000189978 N767N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr9:113538207 G>A maps to ENST00000189978 W448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr9:113547281 G>A maps to ENST00000189978 W530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr9:113530264 G>C maps to ENST00000189978 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr9:113530255 G>C maps to ENST00000189978 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:8041390 G>A maps to NM_201280.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr6:8064507 G>T maps to NM_201280.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr6:8041459 C>T maps to NM_201280.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr16:88721705 G>C maps to NM_002461.1 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:110024577 T>C maps to NM_001114185.1 H217H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:29852915 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:29845299 C>T maps to NM_017458.3 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:29845310 C>A maps to NM_017458.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:29858703 C>T maps to NM_017458.3 Q818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr16:29858531 G>A maps to NM_017458.3 Q760Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr16:29857243 G>C maps to NM_017458.3 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr21:42812950 C>A maps to NM_001144925.1 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr21:42823169 G>A maps to NM_001144925.1 K503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr21:42813763 G>A maps to NM_001144925.1 Q284Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr21:42813769 C>A maps to NM_001144925.1 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr21:42824619 G>T maps to NM_001144925.1 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr21:42778861 C>T maps to NM_002463.1 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr21:42762622 G>A maps to NM_002463.1 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr21:42762520 G>A maps to NM_002463.1 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr21:42780075 G>A maps to NM_002463.1 K688K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr21:42754397 C>T maps to NM_002463.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:3242585 C>G did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:3239494 T>C did not map to a codon.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr23:3238722 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr23:3239349 G>A did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:3229320 G>A did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:3239767 T>A did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr23:3241400 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr23:3239560 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr23:3239740 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr23:3239743 C>T did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr23:3238915 G>C did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:3229460 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:3241796 G>A did not map to a codon.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr23:3240253 G>A did not map to a codon.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr23:3241553 G>C did not map to a codon.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr23:3240253 G>C did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr23:3235239 C>A did not map to a codon.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr23:3238515 G>C did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:3248281 G>A did not map to a codon.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr23:3240446 G>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:3242730 A>G did not map to a codon.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr23:3239788 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:3238722 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:3240311 C>T did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr23:3235277 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:3240958 T>C did not map to a codon.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr23:3242344 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:3239951 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:3240667 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr23:3241286 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr23:3239012 A>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:1290311 G>A maps to NM_032348.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr19:54376941 G>A maps to NM_001020818.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:54377145 C>T maps to NM_001020818.1 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr19:54377238 C>T maps to NM_001020818.1 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:54377328 C>T maps to NM_001020818.1 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr6:135515529 C>T maps to NM_001130173.1 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:4455915 C>T maps to NM_001105538.1 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:4451466 G>A maps to NM_001105538.1 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr17:4448565 C>T maps to NM_001105538.1 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:4458574 C>G maps to NM_001105538.1 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:4442928 C>T maps to NM_001105538.1 Q1256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:4443773 C>G maps to NM_001105538.1 L1101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr17:4446306 G>A maps to NM_001105538.1 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr17:4453498 G>A maps to NM_001105538.1 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr8:67514655 G>A maps to NM_001080416.2 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr8:67504748 C>A maps to NM_001080416.2 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr8:67478984 G>C maps to NM_001080416.2 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:67507964 C>T maps to NM_001080416.2 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr8:67514679 C>T maps to NM_001080416.2 W33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr20:42320808 T>C maps to NM_002466.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr12:102045133 C>T maps to NM_002465.2 Q497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr12:102040592 C>T maps to NM_002465.2 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr12:102060549 T>C maps to ENST00000441232 N770N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr12:102040657 C>T maps to NM_002465.2 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr19:50939407 C>T maps to NM_004533.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr19:50961862 C>G maps to NM_004533.3 A786A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:50967706 G>A maps to NM_004533.3 S1111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:50967745 C>T maps to NM_004533.3 N1124N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr19:50967790 T>G did not map to a codon.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr19:50958851 C>T maps to NM_004533.3 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr19:50947073 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr19:50945441 C>T maps to NM_004533.3 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr19:50964950 C>T maps to NM_004533.3 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr19:50962450 C>T maps to NM_004533.3 F893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr19:50958428 C>T maps to NM_004533.3 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr11:47364472 G>A maps to ENST00000399249 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:47354824 G>A maps to ENST00000399249 L1084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:203140595 G>T maps to NM_004997.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr1:203138037 G>C maps to NM_004997.2 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr8:128751083 G>T maps to NM_002467.4 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:128750660 G>A maps to NM_002467.4 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:77669734 G>A maps to NM_015057.4 V3319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:77852998 T>C maps to NM_015057.4 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr13:77642918 G>C maps to NM_015057.4 V3984V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:77651515 G>A maps to NM_015057.4 L3831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr13:77642912 T>C maps to NM_015057.4 E3986E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr13:77847639 G>T maps to NM_015057.4 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr13:77714226 C>T maps to NM_015057.4 Q2491Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr13:77765948 C>G did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr13:77780797 C>T maps to NM_015057.4 L1193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr13:77671943 G>A maps to NM_015057.4 I3115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr13:77759425 C>A maps to NM_015057.4 E1511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr13:77629764 C>G maps to NM_015057.4 V4525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr13:77671967 T>C maps to NM_015057.4 P3107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr13:77748453 G>C maps to NM_015057.4 L1881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr13:77641942 G>A maps to NM_015057.4 S4076S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:48604700 C>T maps to NM_032133.4 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:48600298 G>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr17:48586016 C>T maps to NM_032133.4 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr17:48593986 G>T maps to NM_032133.4 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:48606083 G>A maps to NM_032133.4 V855V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:16082290 C>T maps to NM_005378.4 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:16085690 C>T maps to NM_005378.4 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:16082800 G>T maps to NM_005378.4 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr2:16082731 G>T maps to NM_005378.4 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr6:153043096 G>C maps to NM_025107.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr15:48444121 G>A maps to NM_016132.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr11:69062896 G>T maps to NM_138768.2 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr11:69062934 G>C maps to NM_138768.2 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr12:81111063 C>T maps to NM_005593.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr12:81111187 C>T maps to NM_005593.2 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr12:81111213 C>G maps to NM_005593.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:81111210 C>T maps to NM_005593.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr12:81110944 C>T maps to NM_005593.2 R35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr12:81101954 C>T maps to NM_002469.2 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr12:81101623 C>A maps to NM_002469.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr17:10411686 C>T maps to NM_005963.3 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr17:10409365 A>G maps to NM_005963.3 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:10399383 C>T maps to NM_005963.3 L1684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr17:10401050 C>T maps to NM_005963.3 K1455K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:10419629 G>A maps to NM_005963.3 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr17:10415815 G>A maps to NM_005963.3 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr17:10398334 C>T maps to NM_005963.3 T1793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr17:10415239 G>A maps to NM_005963.3 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:10415429 G>A maps to NM_005963.3 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr17:10409223 G>A maps to NM_005963.3 V693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr17:8449912 G>A maps to ENST00000360416 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr17:8449972 C>T maps to ENST00000360416 Q389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr17:8396108 C>T maps to ENST00000360416 Q1481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:8422096 C>A maps to ENST00000360416 E786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr17:8409807 C>T did not map to a codon.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr17:8417199 C>T maps to ENST00000360416 K839K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr17:8387497 C>T maps to ENST00000360416 K1711K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr17:8396287 C>A maps to ENST00000360416 E1422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:15841994 C>A maps to NM_001040114.1 E704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:15835628 C>T maps to NM_001040114.1 Q887Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr16:15833946 C>T maps to NM_001040114.1 E993E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr16:15851722 C>T maps to NM_001040114.1 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:15931777 G>C maps to NM_001040114.1 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:15932088 G>A maps to NM_001040114.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr16:15820797 C>T maps to NM_001040114.1 K1262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr16:15829284 C>G maps to NM_001040114.1 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr16:15829308 C>T maps to NM_001040114.1 Q1147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr17:10248879 C>A maps to NM_003802.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:10248813 G>T maps to NM_003802.2 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:10265465 G>A maps to NM_003802.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr17:10204268 C>T maps to NM_003802.2 *1939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:10212868 C>T maps to NM_003802.2 K1645K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr17:10216602 A>T maps to NM_003802.2 Y1351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:10253987 G>A maps to NM_003802.2 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr17:10216004 C>T maps to NM_003802.2 S1417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:10235463 G>T maps to NM_003802.2 L750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr17:10231293 A>G maps to NM_003802.2 F860F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:10216042 C>A maps to NM_003802.2 E1405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:10243491 C>G maps to NM_003802.2 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr17:10235526 G>C maps to NM_003802.2 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:50764748 G>A maps to NM_001145809.1 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr19:50774700 G>A maps to NM_001145809.1 A1023A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr19:50804979 G>A maps to NM_001145809.1 G1844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr19:50804980 C>A maps to NM_001145809.1 R1845R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr19:50789752 G>A maps to NM_001145809.1 E1518E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr19:50753031 C>T maps to NM_001145809.1 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:50792751 A>G maps to NM_001145809.1 A1604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr3:108158679 C>T maps to NM_014981.1 E1013E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:108102560 G>A maps to NM_014981.1 Q1903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:108218326 G>A maps to NM_014981.1 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr3:108133161 G>C maps to NM_014981.1 S1374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:108135693 C>A maps to NM_014981.1 E1325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr3:108110645 C>A maps to NM_014981.1 L1817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr17:10427829 G>A maps to NM_017534.5 Q1710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr17:10430321 G>C maps to NM_017534.5 S1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:10442617 C>T maps to NM_017534.5 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr17:10448677 G>A maps to NM_017534.5 Q164*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-A2I4-01A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:10438397 G>A maps to NM_017534.5 F724F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr17:10436849 G>A maps to NM_017534.5 T760T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:10432499 C>T maps to NM_017534.5 Q1111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:10535903 G>C maps to NM_002470.2 L1615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:10539066 C>T maps to NM_002470.2 L1320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:10532976 C>T maps to NM_002470.2 A1911A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:10547727 C>T maps to NM_002470.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr17:10532970 G>A maps to NM_002470.2 I1913I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:10542948 G>C maps to NM_002470.2 L951L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr17:10545812 G>A maps to NM_002470.2 N603N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr17:10364371 C>G did not map to a codon.
Sequencing variant TCGA-CF-A47W-01A-11D-A23U-08 chr17:10351272 G>T maps to NM_017533.2 I1609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:10362719 G>A maps to NM_017533.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:10363274 G>T maps to NM_017533.2 I470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr17:10363352 G>A maps to NM_017533.2 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr17:10369589 G>A maps to NM_017533.2 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr17:10359804 G>A maps to NM_017533.2 F655F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr17:10346753 G>A maps to NM_017533.2 Q1920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr17:10358114 G>A maps to NM_017533.2 F816F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr17:10357085 G>T maps to NM_017533.2 I936I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:23865620 G>A maps to NM_002471.3 F767F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr14:23869938 G>A maps to NM_002471.3 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr14:23863378 G>A maps to NM_002471.3 I861I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr14:23856970 A>C maps to NM_002471.3 L1507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr14:23856976 C>T maps to NM_002471.3 K1505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr14:23855640 C>G maps to NM_002471.3 L1614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr14:23869929 G>A maps to NM_002471.3 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr14:23870045 G>A maps to NM_002471.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr14:23887504 A>C maps to NM_000257.2 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr14:23897827 G>A maps to NM_000257.2 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr14:23884263 G>A maps to NM_000257.2 N1833N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:23899053 G>A maps to NM_000257.2 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr14:23894223 C>T maps to NM_000257.2 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr14:23890202 G>A maps to NM_000257.2 L1100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr14:23886467 C>T maps to NM_000257.2 Q1471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr14:23902830 G>C maps to NM_000257.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr14:23894579 G>A maps to NM_000257.2 D778D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:33577697 C>T maps to NM_020884.3 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr20:33588233 C>T maps to NM_020884.3 T1682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr20:33574743 C>A maps to NM_020884.3 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:33568427 C>T maps to NM_020884.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr20:33587434 G>A maps to NM_020884.3 E1576E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr20:33575450 C>T maps to NM_020884.3 Y455Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr17:10302860 C>A maps to NM_002472.2 A1287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:10315692 G>A maps to NM_002472.2 I470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr22:36681273 G>A maps to NM_002473.4 V1792V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr22:36697581 G>A maps to NM_002473.4 Q877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:36690983 C>T maps to NM_002473.4 T1208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:36698619 G>A maps to NM_002473.4 F831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:36684829 C>A maps to NM_002473.4 R1571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr22:36685340 G>A maps to NM_002473.4 L1449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr22:36708230 C>A maps to NM_002473.4 E531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr22:36744961 G>C maps to NM_002473.4 S107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr22:36681756 C>A maps to NM_002473.4 E1741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr22:36745233 G>A maps to NM_002473.4 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr22:36680508 C>G maps to NM_002473.4 L1844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr22:36708191 C>A maps to NM_002473.4 E544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr22:36708192 C>A maps to NM_002473.4 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr22:36715630 G>A maps to NM_002473.4 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr22:36691012 C>A maps to NM_002473.4 E1199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr22:36681817 C>A maps to NM_002473.4 A1720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr22:36695010 G>A maps to NM_002473.4 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr22:36712696 C>T maps to NM_002473.4 E415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr22:36695027 C>A maps to NM_002473.4 E1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr22:36710360 C>G maps to NM_002473.4 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr22:36680278 G>C maps to NM_002473.4 L1875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr22:36695001 G>A maps to NM_002473.4 L1021L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr2:211158489 C>T maps to NM_079420.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr18:3253277 G>A maps to NM_006471.2 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr18:3255844 A>T maps to NM_006471.2 K149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr17:45297324 C>T maps to NM_002476.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:56547836 G>A maps to NM_002475.4 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr7:44180380 G>A maps to ENST00000457314 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr20:35176534 C>T maps to NM_006097.3 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr6:16145427 G>A maps to NM_013262.3 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr3:123419211 G>A maps to NM_053025.3 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:123419599 C>T maps to NM_053025.3 V905V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:123348339 G>A maps to NM_053025.3 L1699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr3:123383092 C>A maps to NM_053025.3 E1282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr3:123339144 G>C maps to NM_053025.3 S1759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr3:123426707 G>A maps to NM_053025.3 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr3:123419158 A>G maps to NM_053025.3 N1052N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr3:123419167 G>T maps to NM_053025.3 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr3:123419182 G>A maps to NM_053025.3 A1044A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr3:123366123 G>A maps to NM_053025.3 V1522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr20:30419637 C>T maps to NM_033118.3 N519N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr20:30419887 C>T maps to NM_033118.3 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:30409505 C>T maps to NM_033118.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr16:46771855 C>T maps to NM_182493.2 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr16:46766180 C>A maps to NM_182493.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr6:2683269 G>C maps to NM_001012418.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr6:2678482 G>A maps to NM_001012418.3 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr3:169502468 A>T maps to NM_018657.4 K515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:169504459 A>G maps to NM_018657.4 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr5:16681565 C>T maps to NM_012334.2 L1412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr5:16779716 C>T maps to NM_012334.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr5:16672862 G>A maps to NM_012334.2 N1748N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr5:16668555 G>A maps to NM_012334.2 Q1969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:16680070 C>T maps to NM_012334.2 L1509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr5:16935894 A>C did not map to a codon.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr5:16671021 G>A maps to NM_012334.2 A1832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr5:16675229 G>A maps to NM_012334.2 Q1566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr5:16672919 C>T maps to NM_012334.2 L1729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr17:18082088 G>T maps to ENST00000205890 E3500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr17:18028545 G>A did not map to a codon.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr17:18059589 C>T maps to ENST00000205890 F2847F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:18023319 G>A maps to ENST00000205890 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:18045032 G>C maps to ENST00000205890 L1866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr17:18064711 C>T maps to ENST00000205890 L3156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:18042858 C>T maps to ENST00000205890 F1715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:18054745 C>G maps to ENST00000205890 L2564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:18066583 C>G maps to ENST00000205890 L3213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:18049376 C>T maps to ENST00000205890 L2155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr17:18022998 C>T maps to ENST00000205890 Y295Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:18057191 G>A maps to ENST00000205890 K2690K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:18070953 G>A maps to ENST00000205890 R3333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr17:18023271 C>T maps to ENST00000205890 G386G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BT-A3PK-01A-21D-A21Z-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:109672111 A>C maps to NM_015011.1 S861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:109753190 C>T maps to NM_015011.1 R1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr13:109707813 C>G maps to NM_015011.1 S1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr13:109613988 C>T maps to NM_015011.1 Q692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr13:109707787 C>T maps to NM_015011.1 F1038F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:27421805 C>T maps to NM_078471.3 Q1524Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr17:27425436 C>T maps to NM_078471.3 K1269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:27438548 G>A maps to NM_078471.3 H931H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:27419971 C>T maps to NM_078471.3 L1658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:27413463 G>A maps to NM_078471.3 L1948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr17:27493019 G>C maps to NM_078471.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr17:27447753 G>A maps to NM_078471.3 Y536Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr17:27441070 A>G maps to NM_078471.3 D852D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr17:27424303 G>C maps to NM_078471.3 L1389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:27401832 C>T maps to NM_078471.3 L2040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr17:27421745 G>T maps to NM_078471.3 L1544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr17:27445165 C>T maps to NM_078471.3 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr17:27414049 C>T maps to NM_078471.3 Q1872Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr17:27448118 G>A maps to NM_078471.3 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr17:27421757 G>T maps to NM_078471.3 V1540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr22:26242213 G>A maps to ENST00000407587 R1174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr22:26400707 C>A maps to ENST00000407587 S2121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr22:26307007 C>T maps to ENST00000407587 L1787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr22:26422719 G>A maps to ENST00000407587 K2262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr22:26164374 A>G maps to ENST00000407587 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr22:26423016 G>A maps to ENST00000407587 P2361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr22:26423351 C>G maps to ENST00000407587 S2473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr22:26224899 C>A maps to ENST00000407587 R984R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr22:26351203 G>A maps to ENST00000407587 A2012A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr22:26164500 C>G maps to ENST00000407587 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr22:26294299 C>T maps to ENST00000407587 D1567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr17:34856953 G>A maps to NM_001163735.1 A734A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr17:34862864 G>A maps to NM_001163735.1 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr17:34864916 C>A maps to NM_001163735.1 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr17:34856679 G>A maps to NM_001163735.1 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr12:57440402 C>T maps to NM_005379.2 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr12:57441147 C>T maps to NM_005379.2 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:57436894 G>C maps to NM_005379.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr12:57440333 A>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr12:57423251 G>C maps to NM_005379.2 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr2:192225355 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:192194755 G>T did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:192255218 G>C did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:192275842 G>T maps to NM_001130158.1 E940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:192288562 G>A maps to NM_001130158.1 E1096E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr17:1375307 G>A maps to NM_001080779.1 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr17:1378123 G>T maps to NM_001080779.1 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr17:1381473 G>A maps to NM_001080779.1 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr17:1370775 G>A maps to NM_001080779.1 G1021G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr17:1381930 G>A maps to NM_001080779.1 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr17:30980884 G>T maps to NM_015194.1 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:30932241 G>A maps to NM_015194.1 V909V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr17:31203815 G>A maps to NM_015194.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:31076013 G>C maps to NM_015194.1 S493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr17:31087615 G>A maps to NM_015194.1 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr15:59502739 G>A maps to NM_004998.2 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr15:59500903 G>A maps to NM_004998.2 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr15:59445943 G>T maps to NM_004998.2 P975P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr15:59501032 G>A maps to NM_004998.2 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr15:59548520 G>A maps to NM_004998.2 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr15:59500963 G>A maps to NM_004998.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr19:8615578 C>G did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:8609324 G>A maps to NM_012335.3 V460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:8615473 C>T maps to NM_012335.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr19:8615058 G>A maps to NM_012335.3 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr7:45015118 C>T maps to NM_033054.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr7:45004618 G>A maps to NM_033054.2 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr7:45016618 C>T maps to NM_033054.2 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr7:45016594 C>A maps to NM_033054.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr7:45009686 C>T maps to NM_033054.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:109872911 C>T maps to NM_001101421.3 Q696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr12:109865340 G>T maps to NM_001101421.3 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr10:26491922 C>T maps to NM_017433.4 F1539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr10:26492007 C>T maps to NM_017433.4 Q1568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr10:26462804 C>T maps to NM_017433.4 F1204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:26446394 C>T maps to NM_017433.4 R984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr10:26414471 T>C maps to NM_017433.4 Y683Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr10:26462933 G>A maps to NM_017433.4 E1247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr10:26414412 C>T maps to NM_017433.4 R664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr10:26432423 G>A maps to NM_017433.4 E770E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr10:26482182 C>A maps to NM_017433.4 P1496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47W-01A-11D-A23U-08 chr2:171242782 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr2:171356163 C>G maps to NM_138995.3 L1045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr15:52672021 G>C maps to ENST00000358212 S699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr15:52656894 A>G maps to ENST00000358212 T1055T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr15:52667617 G>A maps to ENST00000358212 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr18:47428978 C>A maps to NM_001080467.2 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr18:47581730 G>A maps to NM_001080467.2 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr18:47479628 C>A did not map to a codon.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr18:47379926 C>T maps to NM_001080467.2 E1371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr18:47375961 G>A maps to NM_001080467.2 Y1430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr18:47369613 C>T maps to NM_001080467.2 L1536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr18:47500757 G>C maps to NM_001080467.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr18:47581661 T>C maps to NM_001080467.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr15:52553306 C>T maps to NM_018728.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr15:52511966 T>A maps to NM_018728.3 G1258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr15:52505467 G>T maps to NM_018728.3 S1353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr15:52564860 T>C maps to NM_018728.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr15:52534273 C>A maps to NM_018728.3 G843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr15:52537622 G>A maps to NM_018728.3 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr15:52531976 G>A maps to NM_018728.3 Q886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr15:52527931 G>C maps to NM_018728.3 S966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr6:76558180 C>T maps to ENST00000428345 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr6:76600962 A>G maps to ENST00000428345 A962A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr11:76910744 C>T maps to NM_000260.3 D1578D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr11:76873177 C>G maps to NM_000260.3 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr11:76901827 G>T maps to NM_000260.3 T1279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:76903268 C>T maps to NM_000260.3 L1366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:76867747 C>A maps to NM_000260.3 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr11:76869396 C>T maps to NM_000260.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr2:128335736 C>T maps to ENST00000389524 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:128342381 G>C maps to ENST00000389524 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:128351215 G>A maps to ENST00000389524 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr2:128350490 C>A maps to ENST00000389524 G705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:128324289 C>T maps to ENST00000389524 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr2:128327426 C>A maps to ENST00000389524 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr2:128338347 C>G maps to ENST00000389524 S344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr15:72270609 G>A maps to ENST00000424560 I582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr15:72193533 G>A maps to ENST00000424560 Q1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr15:72338070 T>C maps to ENST00000424560 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr15:72197347 C>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr15:72141296 C>G maps to ENST00000424560 L2313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr15:72338676 G>A maps to ENST00000424560 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:17305658 C>G maps to NM_004145.3 V1141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:17213294 C>G maps to NM_004145.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr19:17321179 G>A maps to NM_004145.3 E1929E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:17323117 G>T maps to NM_004145.3 *2158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr19:17213123 C>A maps to NM_004145.3 Y199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr19:17295780 C>T maps to NM_004145.3 I827I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:17265156 G>A maps to NM_004145.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:171621259 C>T maps to NM_000261.1 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:171605523 C>T maps to NM_000261.1 E352E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:171621211 C>T maps to NM_000261.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr1:171621640 G>T maps to NM_000261.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr1:171621559 C>T maps to NM_000261.1 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr17:12656530 T>A maps to NM_001146312.1 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:12569537 G>C maps to NM_001146312.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr10:95163794 C>G maps to NM_013451.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr10:95113640 G>C maps to NM_013451.3 V1136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr10:95157002 C>T maps to ENST00000371489 W445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr10:95072941 G>A maps to NM_013451.3 H1908H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr10:95139624 G>T maps to NM_013451.3 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr10:95110965 G>A maps to NM_013451.3 L1303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr10:95079753 C>A maps to NM_013451.3 E1825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:203054921 C>A maps to NM_002479.4 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr18:3187532 C>A maps to NM_003803.3 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr18:3131436 G>C maps to NM_003803.3 V814V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr18:3089556 C>T maps to NM_003803.3 R1349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr18:3119939 G>A maps to NM_003803.3 N1015N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr18:3193939 G>A maps to NM_003803.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr18:3067370 C>T maps to NM_003803.3 K1649K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr18:3168908 A>G maps to NM_003803.3 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr18:3134822 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr18:3116331 C>T maps to NM_003803.3 L1100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr8:2088810 T>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr8:2054134 C>G maps to NM_003970.2 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr8:2071162 C>G maps to NM_003970.2 L1164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:2090322 G>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr8:2037889 G>C maps to NM_003970.2 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr8:2046708 C>G maps to NM_003970.2 S779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr8:2005856 C>A maps to NM_003970.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr8:2044114 G>A maps to NM_003970.2 T718T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:24383901 G>A maps to ENST00000330966 I1425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:24392392 G>A maps to ENST00000330966 L1177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr1:24419479 C>T maps to ENST00000330966 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:24408601 G>C maps to ENST00000330966 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:24411102 G>A maps to ENST00000330966 Q610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:24388443 G>C maps to ENST00000330966 S1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:137222945 C>T maps to NM_006790.2 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMW-01A-11D-A42E-08 chr5:137222945 C>T maps to NM_006790.2 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr4:120107258 T>C maps to NM_016599.3 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr5:150056364 C>G maps to NM_133371.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr5:150056331 C>T maps to NM_133371.3 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr10:69926393 G>A maps to NM_032578.2 E648E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr10:69925570 G>C maps to NM_032578.2 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:69902715 G>T maps to NM_032578.2 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:69934017 G>A maps to NM_032578.2 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:69881471 G>T maps to NM_032578.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr10:69961598 G>A maps to NM_032578.2 K1169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr10:69881234 C>T maps to NM_032578.2 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:46404902 C>T maps to NM_001012643.2 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr3:40192631 C>T maps to NM_015460.2 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:59142622 C>T maps to NM_001085487.1 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr16:31141846 C>T maps to NM_182958.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:47886482 G>A maps to NM_007067.4 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr17:47874208 G>A maps to NM_007067.4 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:47874208 G>C maps to NM_007067.4 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:47874110 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:47904113 C>T maps to NM_007067.4 Q563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr8:41798737 G>A maps to NM_006766.3 L887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr8:41906304 G>C maps to NM_006766.3 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr8:41798545 G>C maps to NM_006766.3 L951L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr8:41800465 G>A maps to NM_006766.3 Q761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr10:76602803 C>T maps to NM_012330.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr10:76719768 G>A maps to NM_012330.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr10:76735714 G>A maps to NM_012330.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr10:76602977 G>A maps to NM_012330.2 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr10:76735804 T>C maps to NM_012330.2 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr10:76602842 C>T maps to NM_012330.2 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr20:62871219 C>T maps to NM_004535.2 L1067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:62838959 C>G maps to NM_004535.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr20:62839181 A>G maps to NM_004535.2 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr20:62839355 G>A maps to NM_004535.2 E269E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr20:62839058 C>T maps to NM_004535.2 N170N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr2:1843039 G>A maps to ENST00000399161 D987D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr2:1983501 C>T maps to ENST00000399161 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:1914103 C>G maps to ENST00000399161 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:1983497 G>A maps to ENST00000399161 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:1926916 G>A maps to ENST00000399161 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr2:1983317 C>A maps to ENST00000399161 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr2:1983318 C>T maps to ENST00000399161 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr2:1921091 C>T maps to ENST00000399161 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:1926558 C>A maps to ENST00000399161 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:1926559 C>A maps to ENST00000399161 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr2:1926870 C>A maps to ENST00000399161 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:1926394 G>T maps to ENST00000399161 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr19:59073927 G>A maps to NM_198055.1 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:59073564 C>T maps to NM_198055.1 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr19:59074421 C>A maps to NM_198055.1 E408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr19:59073867 C>A maps to NM_198055.1 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr16:48595965 G>C maps to NM_153029.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr16:48596025 C>T maps to NM_153029.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:40103905 G>A maps to NM_018177.3 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr4:40122363 C>A maps to NM_018177.3 S878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr4:40123291 C>T maps to NM_018177.3 N1187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:40123216 T>C maps to NM_018177.3 I1162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr4:40104487 G>A maps to NM_018177.3 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr4:40122319 C>A maps to NM_018177.3 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:40133518 G>A maps to NM_018177.3 V1542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:33017212 C>T maps to NM_033111.3 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:33110632 C>A maps to ENST00000505213 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr21:30255350 T>C maps to NM_013240.3 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr21:30257655 C>T maps to NM_013240.3 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr21:30255332 A>T maps to NM_013240.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr21:30255319 G>A maps to NM_013240.3 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr21:30257610 G>A maps to NM_013240.3 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr21:30257652 G>A maps to NM_013240.3 N5N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr23:153199421 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr23:153197541 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr23:153197563 G>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:153199890 A>T did not map to a codon.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr4:80246701 G>A maps to NM_032693.2 H110H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr4:80246860 C>A maps to NM_032693.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:140299922 G>A maps to NM_057175.3 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr4:140265456 C>T maps to NM_057175.3 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr13:41910843 C>T maps to NM_024561.4 C322C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr13:41941785 C>G maps to NM_024561.4 S584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr12:112530904 G>A maps to NM_024953.3 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:112477110 G>T maps to NM_024953.3 Y857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr12:112512525 G>C maps to NM_024953.3 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr12:112509732 T>C maps to NM_024953.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr7:117828406 C>T maps to NM_016200.4 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr11:89924899 G>A maps to NM_005467.3 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr11:89896182 C>T maps to NM_005467.3 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr11:89885587 G>A maps to NM_005467.3 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr11:89892445 G>A maps to NM_005467.3 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:89880530 A>G maps to NM_005467.3 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr11:89880587 A>G maps to NM_005467.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr11:64825409 C>A maps to ENST00000340252 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr3:175293968 A>G maps to NM_207015.2 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:174814755 C>T maps to NM_207015.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr3:174815022 C>T maps to NM_207015.2 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr2:191535075 C>T maps to NM_005966.3 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr12:57114254 C>T maps to NM_001113203.1 Q353Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:57112903 G>A maps to NM_001113203.1 Q804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr12:57113936 T>A maps to NM_001113203.1 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr12:57112271 C>T maps to NM_001113203.1 V1014V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr12:57114256 G>A maps to NM_001113203.1 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr12:57113651 C>T maps to NM_001113203.1 K554K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:13246851 C>T maps to NM_052876.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:13247178 C>T maps to NM_052876.2 Y360Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:138903718 G>A maps to NM_144653.3 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:1696731 G>A maps to ENST00000344463 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:1686042 C>T maps to ENST00000344463 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr11:71191847 C>T maps to NM_018161.4 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr16:66847710 G>C maps to ENST00000359087 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr4:164054327 G>C maps to NM_138386.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr22:42456282 T>A maps to NM_000262.2 *412C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr22:42463780 G>A maps to NM_000262.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr22:42461822 G>A maps to NM_000262.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr22:42463219 G>A maps to NM_000262.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr22:42461876 G>A maps to NM_000262.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:71298937 C>T maps to NM_017567.4 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:40689535 G>A maps to NM_000263.3 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:5083317 C>T maps to NM_016256.3 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr17:42082123 G>C maps to NM_153006.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:130829326 C>T maps to NM_197956.3 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr9:130826117 C>T maps to NM_197956.3 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:70308613 C>T maps to NM_004536.2 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:70308504 C>A maps to NM_004536.2 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr5:70308244 G>A maps to NM_004536.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr5:70308421 G>A maps to NM_004536.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr5:70308223 G>C maps to NM_004536.2 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr13:102029157 C>T maps to NM_052867.2 W179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr13:101712283 C>G maps to NM_052867.2 L1597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr13:102051407 G>A maps to NM_052867.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr13:101763500 G>A maps to NM_052867.2 Q757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr13:102047608 G>A maps to NM_052867.2 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr13:101910814 G>A maps to NM_052867.2 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr13:101735204 A>G maps to NM_052867.2 P1240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr12:7947072 C>T maps to NM_024865.2 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:46417756 G>A maps to NM_001029861.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr9:100845192 C>T maps to NM_018946.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr9:100839225 G>A maps to NM_018946.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr12:76461247 G>A maps to NM_139207.2 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr12:76462751 G>A maps to NM_139207.2 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:72433763 C>G did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:72434144 C>T did not map to a codon.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr23:72433811 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr23:72434068 C>A did not map to a codon.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr23:72434010 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr23:92927447 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr23:92926916 C>G did not map to a codon.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr23:92928229 G>A did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr23:92927608 G>T did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr23:92927613 T>C did not map to a codon.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr23:92927153 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr23:92928049 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:2975839 C>A maps to ENST00000399624 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:2979641 G>A maps to ENST00000399624 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:23375802 A>G maps to ENST00000431864 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr7:102768980 G>C maps to ENST00000455523 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr18:10526137 C>T maps to NM_003826.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr18:10539785 C>T maps to NM_003826.2 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr18:10549049 C>G maps to NM_003826.2 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr8:144660266 G>A maps to ENST00000276844 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr8:144657591 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr19:50862273 G>A maps to NM_004851.1 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr19:50865443 G>C maps to NM_004851.1 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:50864259 C>T maps to NM_004851.1 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr19:50865521 C>T maps to NM_004851.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:80439026 C>T maps to ENST00000374611 Q237*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DK-AA71-01A-31D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr17:80422293 G>A maps to ENST00000374611 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr16:783367 C>A maps to NM_022493.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr16:786282 G>C maps to NM_022493.1 S141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr16:783421 C>T maps to NM_022493.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:787257 G>A maps to NM_022493.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr15:60715833 C>G maps to NM_024611.4 *983S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr18:55273931 C>G maps to NM_004539.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr18:55283165 G>A maps to NM_004539.3 Y45Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr18:55273853 G>A maps to NM_004539.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:78177017 C>T maps to NM_024678.4 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:78285428 C>T maps to NM_024678.4 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr11:34139780 C>G maps to NM_024662.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:34167636 G>A maps to NM_024662.2 K992K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr11:34139974 G>C maps to NM_024662.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:34167702 G>A maps to NM_024662.2 K1014K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr11:34139989 G>A maps to NM_024662.2 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr11:34145863 G>T maps to NM_024662.2 E342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr16:3534737 G>C maps to NM_024845.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:50334453 C>A maps to NM_012191.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr4:2065499 G>A maps to ENST00000423729 W192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr17:72769089 G>C maps to NM_015654.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr17:72767985 G>A maps to NM_015654.3 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:72767988 C>G maps to NM_015654.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr1:201749602 C>G maps to ENST00000367296 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:201754452 G>C maps to ENST00000367296 R940R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:201752698 C>T maps to ENST00000367296 F841F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:201757680 C>T maps to ENST00000367296 G1027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:201752842 G>A maps to ENST00000367296 Q889Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:201788963 G>C did not map to a codon.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr11:20057558 C>T maps to ENST00000396087 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr11:19955346 G>A maps to ENST00000396087 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:20122582 C>A maps to ENST00000396087 I2153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:20124943 G>A maps to ENST00000396087 K2246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr11:20112512 C>G maps to ENST00000396087 L1926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:20066679 C>T maps to ENST00000396087 F1145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr11:20119139 C>T maps to ENST00000396087 V2069V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr11:19901578 C>T maps to ENST00000396087 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr11:19735318 C>T maps to ENST00000396087 H26H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr11:20113768 G>T maps to ENST00000396087 L1949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:78225382 G>T maps to NM_014903.4 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr12:78400994 G>A maps to NM_014903.4 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:78583818 A>G maps to NM_014903.4 P2015P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr12:78582522 T>G maps to NM_014903.4 V1985V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr12:78444903 C>G maps to NM_014903.4 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr12:78400289 T>G maps to NM_014903.4 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr12:78360076 T>C maps to NM_014903.4 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr12:78570934 C>T maps to NM_014903.4 F1713F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:15448381 T>A maps to NM_015909.2 R1585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr2:15307237 C>T maps to NM_015909.2 V2350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr2:15629086 G>A maps to NM_015909.2 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr2:15493687 G>A maps to NM_015909.2 L1360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:15415870 G>A maps to NM_015909.2 Q1821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr13:35619478 C>T maps to ENST00000400445 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr13:36229745 G>A maps to ENST00000400445 W2720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr13:35619478 C>T maps to ENST00000400445 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr13:35731302 G>T maps to ENST00000400445 E914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr13:35926316 T>C maps to ENST00000400445 A2012A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr13:36129145 C>T maps to ENST00000400445 R2277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr13:36242530 G>A maps to ENST00000400445 Q2875Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr2:204002916 C>G maps to NM_001114132.1 S1504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr2:204000761 C>T maps to NM_001114132.1 F1363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr2:204058598 C>T maps to NM_001114132.1 Q2306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr2:204022420 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:204037540 A>T maps to NM_001114132.1 V2067V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:47044730 G>A maps to NM_015175.1 V1884V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr3:47040468 G>A maps to NM_015175.1 L1135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr3:47044007 C>T maps to NM_015175.1 Q1767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr3:47036910 C>T maps to NM_015175.1 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:47040206 C>T maps to NM_015175.1 S1074S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:90967565 G>A maps to NM_002485.4 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr8:90995000 C>G maps to NM_002485.4 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:16918402 G>C maps to NM_017940.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr1:16907360 G>A maps to NM_017940.3 D490D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr1:16893820 T>A maps to NM_017940.3 K898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr1:16918398 C>A maps to NM_017940.3 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:16918402 G>A maps to NM_017940.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr1:16892176 G>C maps to NM_017940.3 S1006S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:16918351 C>T maps to NM_017940.3 Q55Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr1:16914284 G>A maps to NM_017940.3 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr1:16893777 G>C maps to NM_017940.3 S912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr1:16907243 G>A maps to NM_017940.3 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr1:16902828 C>T maps to NM_017940.3 Q684Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr1:16914284 G>A maps to NM_017940.3 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:16902936 C>T maps to NM_017940.3 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:145296563 C>G maps to NM_001039703.4 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:145293518 C>G maps to NM_001039703.4 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr1:148004751 G>C maps to ENST00000310701 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr1:148015634 A>C maps to ENST00000310701 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr1:148009422 C>G maps to ENST00000310701 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:148025825 C>T maps to ENST00000310701 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:21795328 C>G maps to NM_032264.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr1:21798094 A>G maps to NM_032264.2 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:21799932 C>A maps to NM_032264.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:21771613 G>A maps to NM_032264.2 W12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:41341648 G>A maps to NM_005899.3 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:41341606 C>T maps to NM_005899.3 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr17:41341804 C>T maps to NM_005899.3 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:102731641 G>A maps to NM_032041.2 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr8:102731781 C>A maps to NM_032041.2 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr11:113102513 C>T maps to ENST00000316851 Q412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:113105785 C>T maps to ENST00000316851 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr11:113140943 G>A maps to ENST00000316851 G721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr11:113145991 G>A maps to ENST00000316851 K819K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr21:22696784 C>A maps to NM_004540.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:22881347 G>T maps to NM_004540.2 E752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr21:22881328 C>T maps to NM_004540.2 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr21:22804560 G>A maps to NM_004540.2 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr21:22804537 C>T maps to NM_004540.2 Q531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr19:19334839 C>T maps to NM_004386.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:19359534 G>T maps to NM_004386.2 E1222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr19:19329769 G>A maps to NM_004386.2 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr19:19339265 C>G maps to NM_004386.2 S946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr12:6637913 C>T maps to NM_014865.3 D1123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:6637880 G>A maps to NM_014865.3 A1112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr12:6637408 C>A maps to NM_014865.3 R1072R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr11:134076621 G>A maps to NM_015261.2 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr11:134050983 G>A maps to NM_015261.2 D849D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr11:134050983 G>A maps to NM_015261.2 D849D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr11:134048612 C>A maps to NM_015261.2 E900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:158456890 C>T maps to NM_017760.5 E600E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:158437064 G>C maps to NM_017760.5 S1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr7:158424359 A>C maps to NM_017760.5 *1144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr2:97035168 C>T maps to NM_015341.3 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:97026339 G>C maps to NM_015341.3 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr2:97026363 G>A maps to NM_015341.3 Q501Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:97007491 C>T maps to NM_015341.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr2:97019973 C>T maps to NM_015341.3 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr22:50956081 G>T maps to NM_001185011.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:100418331 G>A maps to NM_002486.4 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:100433474 G>A maps to NM_002486.4 Q789Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:172365739 G>C maps to NM_001146276.1 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:172428675 C>A maps to NM_001146276.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr3:172351621 G>A maps to NM_001146276.1 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:172428786 C>G maps to NM_001146276.1 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr7:74193747 C>G maps to NM_000265.4 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:183533166 T>G did not map to a codon.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr1:183532663 C>G maps to NM_001127651.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr1:183534893 G>A maps to NM_001127651.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr1:183536392 G>T maps to NM_001127651.2 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr22:37266563 C>G maps to NM_013416.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr3:136664518 C>G maps to NM_006153.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr3:136664749 T>C maps to NM_006153.4 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr3:136646887 C>G maps to NM_006153.4 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr2:106509607 C>G maps to NM_001004720.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr2:106498228 G>C maps to NM_001004720.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:106498396 C>T maps to NM_001004720.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr2:183826885 C>T did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:183817957 G>C maps to NM_205842.1 S758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr2:183822294 G>A maps to NM_205842.1 I643I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:183866886 G>A maps to NM_205842.1 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:54920518 C>T maps to NM_005337.4 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr12:54894396 C>T maps to NM_005337.4 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:54911667 C>T maps to NM_005337.4 Y428Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr12:54930821 C>G maps to NM_005337.4 L1056L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr12:54903723 C>T maps to NM_005337.4 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr12:54901656 C>G maps to NM_005337.4 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr2:133887605 G>T maps to NM_207363.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr2:133542703 C>T maps to NM_207363.2 Q560Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr2:133543045 G>C maps to NM_207363.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:133539883 C>T maps to NM_207363.2 Q1500Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:133541788 A>G maps to NM_207363.2 I865I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr2:133543162 C>T maps to NM_207363.2 K407K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr2:133541293 G>A maps to NM_207363.2 T1030T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:133540951 A>G maps to NM_207363.2 T1144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:133542300 C>A maps to NM_207363.2 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr2:133541942 G>C maps to NM_207363.2 S814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:133541947 C>T maps to NM_207363.2 Q812Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:133540509 C>A maps to NM_207363.2 E1292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:133542949 C>T maps to NM_207363.2 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr2:133541236 A>T maps to NM_207363.2 S1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr12:50188729 C>T maps to NM_001037806.3 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr12:50189000 G>C maps to NM_001037806.3 S881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr12:50191117 T>A maps to NM_001037806.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:50195681 C>T maps to NM_001037806.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:50189720 G>T maps to NM_001037806.3 S641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr12:50191060 C>G maps to NM_001037806.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr3:48716071 G>T maps to NM_016453.2 I630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr3:48716385 G>A maps to NM_016453.2 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr19:3198861 C>T maps to NM_020170.3 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr19:3193409 C>T maps to NM_020170.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr2:24914443 C>A maps to NM_003743.4 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr2:24930607 G>T maps to NM_003743.4 E757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr2:24888753 C>T maps to NM_003743.4 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr2:24930107 C>G maps to NM_003743.4 S590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:24933897 G>A maps to NM_003743.4 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr8:71069187 G>C maps to NM_006540.2 S471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr8:71068648 G>A maps to NM_006540.2 Q651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr8:71041011 G>C maps to NM_006540.2 L1176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr20:46279946 C>T maps to NM_181659.2 S1291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr20:46265060 C>G maps to NM_181659.2 S644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr20:46279913 C>T maps to NM_181659.2 F1280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:46264066 G>T maps to NM_181659.2 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:46279913 C>T maps to NM_181659.2 F1280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr20:46265060 C>G maps to NM_181659.2 S644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr20:46281160 C>T maps to NM_181659.2 Q1320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr20:46281813 C>T maps to NM_181659.2 Q1421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr20:46275984 C>T maps to NM_181659.2 Q1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr20:46271058 C>T maps to NM_181659.2 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr10:51585253 G>A maps to NM_001145260.1 E467E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr10:51584707 T>A maps to NM_001145260.1 Y285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr10:51582256 C>T maps to NM_001145260.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr20:44698961 C>G maps to NM_020967.2 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr20:44691997 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr20:44698967 C>G maps to NM_020967.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr20:44691307 G>A maps to NM_020967.2 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr20:44695812 C>T maps to NM_020967.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr20:33356290 C>A maps to NM_014071.2 G164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr20:33364228 C>T maps to NM_014071.2 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr20:33364213 C>T maps to NM_014071.2 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr20:33315092 G>A maps to NM_014071.2 R2040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:126203597 G>A maps to NM_181782.4 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr6:126206330 G>A maps to NM_181782.4 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr6:126236523 C>G maps to NM_181782.4 V714V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr6:126210735 C>T maps to NM_181782.4 N512N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr17:15960897 G>A maps to ENST00000395857 Q2123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr17:16022772 G>A maps to ENST00000395857 R627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:15942888 G>A maps to ENST00000395857 L2286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr17:15952253 G>C maps to ENST00000395857 Y2162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr17:15960869 G>C maps to ENST00000395857 S2132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr17:15984007 G>A maps to ENST00000395857 Q1087*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:16062079 C>T maps to ENST00000395857 E242E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr17:15952193 G>A maps to ENST00000395857 L2182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:16040726 C>G did not map to a codon.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr17:15967418 C>T maps to ENST00000395857 R1743R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr17:15984020 C>T maps to ENST00000395857 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr17:16029477 C>A maps to ENST00000395857 E518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr17:16001792 G>C maps to ENST00000395857 S919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:15973810 G>C maps to ENST00000395857 S1410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr17:15975537 C>T maps to ENST00000395857 L1288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:15952280 C>T maps to ENST00000395857 E2153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr12:124968283 G>C maps to NM_006312.4 S90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr12:124846734 G>A maps to NM_006312.4 Q1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr12:124821404 G>A maps to NM_006312.4 H2010H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:55420602 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:55421385 G>T maps to NM_004829.5 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr6:41309535 T>G maps to NM_004828.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr9:132982044 G>A maps to NM_014286.3 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr9:132980227 C>T maps to NM_014286.3 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:160328024 C>T maps to NM_015331.2 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:160326403 C>T maps to NM_015331.2 Q552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:160327970 C>T maps to NM_015331.2 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr18:2601414 G>A maps to NM_006101.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr18:2606448 G>T maps to NM_006101.2 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr18:2616452 G>A maps to NM_006101.2 Q603Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr18:2616572 A>G maps to NM_006101.2 *643W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr18:2595425 G>T maps to NM_006101.2 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr5:141524151 C>G maps to NM_030571.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr15:23932049 G>A maps to NM_002487.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr15:23931698 C>T maps to NM_002487.2 W222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr15:23931655 C>A maps to NM_002487.2 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr15:23932340 C>T maps to NM_002487.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr15:29561648 C>T maps to NM_138704.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr15:29561447 G>A maps to NM_138704.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr15:29561665 G>A maps to NM_138704.2 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:29561594 C>T maps to NM_138704.2 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr9:140109623 G>A maps to NM_001144026.1 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr9:140100685 G>A maps to NM_001144026.1 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr9:140109117 C>G maps to NM_001144026.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr9:140110129 C>T maps to NM_001144026.1 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr9:140110577 G>A maps to NM_001144026.1 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr23:43809245 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr8:134266784 C>T maps to NM_006096.3 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr14:21486649 G>C maps to NM_201537.1 S276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr20:35310977 C>T maps to ENST00000373803 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr16:58538304 C>G maps to NM_001130487.1 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr16:58538109 C>T maps to NM_001130487.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47S-01A-11D-A23U-08 chr5:149924999 C>T maps to NM_001543.4 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:149932878 C>G maps to NM_001543.4 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr5:149918878 C>A maps to NM_001543.4 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr5:149918798 C>A maps to NM_001543.4 R483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:75567513 G>C maps to NM_003635.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:75567555 G>A maps to NM_003635.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr10:75562821 C>A maps to NM_003635.3 G777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr10:75567714 G>A maps to NM_003635.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr4:119158323 G>A maps to NM_004784.2 K689K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr4:118975892 G>A maps to NM_004784.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr4:118975466 G>A maps to NM_004784.2 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr4:119026231 G>T maps to NM_004784.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr4:115858491 G>A maps to NM_022569.1 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:115997436 G>T maps to NM_022569.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr4:115997246 C>A maps to NM_022569.1 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr4:115997471 C>A maps to NM_022569.1 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr4:115791980 C>T maps to NM_022569.1 V554V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr23:119005902 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr23:119007289 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:240958024 G>A maps to ENST00000404554 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:240961646 T>C maps to ENST00000404554 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr7:10979666 G>T maps to NM_002489.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr7:10979654 C>T maps to NM_002489.2 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:8386221 G>A maps to NM_005001.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:8381529 C>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:124906607 G>C maps to NM_014222.2 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr12:4796180 C>G maps to NM_005002.4 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:4796190 G>T maps to NM_005002.4 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr12:4763542 A>G maps to NM_005002.4 K45K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr12:4768303 T>C maps to NM_005002.4 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr16:23598541 G>C maps to NM_005003.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr16:23596723 A>G maps to NM_005003.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:41679788 G>T maps to NM_016013.2 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr15:41687142 C>A maps to NM_016013.2 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr5:60241094 C>T maps to NM_174889.4 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr6:97344706 T>C maps to NM_014165.3 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:92588064 C>T maps to NM_004545.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr16:2011250 C>T maps to NM_004548.2 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:2011283 G>A maps to NM_004548.2 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr23:47004012 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr7:140404732 G>C maps to NM_004546.2 *106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr2:201943721 A>G maps to NM_002491.2 K39K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr3:120315334 G>A maps to NM_004547.5 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:120315259 C>T maps to NM_004547.5 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr3:179336234 C>T maps to NM_002492.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr10:102286788 C>T maps to NM_005004.2 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:125555326 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr8:125555399 G>A maps to NM_005005.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr4:140216199 G>A maps to NM_001184990.1 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr1:161180098 G>A maps to NM_004550.4 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr1:161172213 C>A maps to NM_004550.4 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:47605942 G>A maps to NM_004551.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr19:1388559 C>T maps to NM_024407.4 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr19:1388835 C>T maps to NM_024407.4 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr11:67803984 G>A maps to NM_002496.3 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr11:67378015 G>A maps to NM_007103.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr11:67378661 G>C maps to NM_007103.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr21:44329052 C>G maps to NM_021075.3 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr2:152471029 C>T maps to NM_001164507.1 P3787P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr2:152496475 C>T maps to NM_001164507.1 L2928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:152470789 A>G maps to NM_001164507.1 D3867D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr2:152536297 A>G maps to NM_001164507.1 Y1064Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:152492770 C>T maps to NM_001164507.1 A3024A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:152512533 C>A maps to NM_001164507.1 E2167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr2:152487761 C>T maps to NM_001164507.1 L3171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:152553183 T>C maps to NM_001164507.1 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:152468804 C>G maps to NM_001164507.1 L3900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr2:152342362 G>A maps to NM_001164507.1 Q8497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr2:152394481 G>T maps to NM_001164507.1 Y7002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:152470906 C>T maps to NM_001164507.1 K3828K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr2:152348792 C>A maps to NM_001164507.1 V8292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr2:152418631 G>A maps to NM_001164507.1 Q6330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:152529143 G>A maps to NM_001164507.1 F1346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:152404174 G>C maps to NM_001164507.1 V6745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:152584364 G>T maps to NM_001164507.1 S45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:152348671 G>A maps to NM_001164507.1 Q8333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:152426864 G>A maps to NM_001164507.1 Y5720Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:152579931 C>G maps to NM_001164507.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr2:152467028 C>T did not map to a codon.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr10:21102871 G>C maps to ENST00000430741 S783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr10:21158752 G>A maps to ENST00000430741 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr10:21462716 C>A maps to NM_213569.2 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr10:21120437 G>A maps to ENST00000430741 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr10:21139389 T>A maps to ENST00000430741 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:84014686 G>A maps to NM_019065.2 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr20:32246631 G>A maps to NM_031232.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr12:8248684 G>C maps to NM_015509.3 *276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:8245361 C>G maps to NM_015509.3 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr1:16767291 C>G maps to NM_018090.4 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:16767291 C>T maps to NM_018090.4 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:97345757 C>G maps to NM_001135175.1 S644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr15:56132915 A>G maps to ENST00000508342 Y1035Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr15:56208870 G>A maps to ENST00000508342 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr15:56208208 G>C maps to ENST00000508342 S274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr15:56152721 G>T maps to ENST00000508342 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr15:56144666 T>G maps to ENST00000508342 V786V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr18:55996292 C>T maps to NM_001144967.1 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr14:24687355 G>A maps to NM_006156.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:11190712 G>C maps to NM_006403.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:11185844 C>T maps to NM_006403.3 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr6:11190346 C>T maps to NM_006403.3 Q585Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr6:11185603 G>A maps to NM_006403.3 Q766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr22:29885131 A>T maps to NM_021076.3 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr8:24813081 G>A maps to ENST00000221169 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr8:24771629 G>A maps to NM_005382.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr8:24775170 G>A maps to NM_005382.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr8:24771305 G>A did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr8:24774735 C>T maps to NM_005382.2 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr8:24771449 G>A maps to NM_005382.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr1:72400954 C>T maps to NM_173808.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr15:75641327 G>T maps to NM_024608.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr4:178243641 G>A maps to NM_018248.2 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr4:178281776 C>T maps to NM_018248.2 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr4:178274876 T>C maps to NM_018248.2 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr4:178274822 G>A maps to NM_018248.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr4:170322821 C>T maps to ENST00000507142 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr3:27349405 G>C maps to ENST00000396636 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:130799265 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:130947484 G>T maps to NM_024800.4 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr3:130884306 C>T maps to NM_024800.4 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr3:130887718 G>T maps to NM_024800.4 E408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr3:130887754 G>T maps to NM_024800.4 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr3:130828670 C>T maps to NM_024800.4 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr13:52718873 G>C maps to NM_002498.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr3:52797517 C>T maps to NM_003157.4 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr3:52778312 T>C maps to NM_003157.4 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr13:52657480 G>C maps to NM_199289.1 S496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:52660444 C>A maps to NM_199289.1 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr13:52661551 C>T maps to NM_199289.1 Q438Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr13:52646134 C>T maps to NM_199289.1 K623K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr9:127113224 G>A maps to NM_001166171.1 *348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr9:127101892 C>T maps to NM_001166171.1 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:198288555 T>G maps to NM_133494.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr17:27065213 G>A maps to NM_178170.2 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr17:27068431 G>A maps to NM_178170.2 E631E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr17:27062256 G>A did not map to a codon.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr14:75568450 G>C maps to NM_033116.4 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr11:21250876 G>A did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr11:21592404 T>C maps to NM_006157.3 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:21592377 C>T maps to NM_006157.3 C683C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:21581918 C>T maps to NM_006157.3 C657C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:20940865 A>T maps to NM_006157.3 K249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr11:20699583 C>T maps to NM_006157.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr11:20948922 G>T maps to NM_006157.3 G277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr11:20939762 G>T maps to NM_006157.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:44917076 A>G maps to NM_001145107.1 C715C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr12:45173748 G>C maps to NM_001145107.1 S181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr12:44926495 C>A maps to NM_001145107.1 E608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:212617720 G>A maps to NM_013349.4 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:73409169 C>T maps to NM_002499.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr15:73528730 C>T maps to NM_002499.3 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr15:73558735 G>C maps to NM_002499.3 V826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr1:156641549 G>C maps to NM_006617.1 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:156642911 G>T maps to NM_006617.1 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:156640273 G>A maps to NM_006617.1 Q1236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:156639167 C>T maps to NM_006617.1 L1604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr1:156642470 C>T maps to NM_006617.1 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:156640229 C>T maps to NM_006617.1 Q1250Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr1:156640304 G>A maps to NM_006617.1 Y1225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr1:156646372 G>A maps to NM_006617.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:156646948 G>C maps to NM_006617.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr10:5496392 C>T maps to NM_001047160.1 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:5497047 G>T maps to NM_001047160.1 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr18:70417769 G>C maps to NM_153181.2 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr18:70451006 G>A maps to NM_153181.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr18:70450928 G>A maps to NM_153181.2 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr18:70461610 C>T maps to NM_153181.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr18:70416324 T>A did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr18:70532045 C>A maps to NM_153181.2 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr18:70532049 G>A maps to NM_153181.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr16:47163189 C>T maps to NM_018092.3 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr6:31827561 C>T maps to NM_000434.3 E394E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr6:31828350 C>A maps to NM_000434.3 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr2:233897533 G>C maps to NM_005383.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr11:74717266 G>A maps to NM_006656.5 Q372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:242757773 C>T maps to NM_001167599.1 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr2:242756192 C>T maps to NM_001167599.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr2:242757401 C>T maps to NM_001167599.1 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr10:105331529 C>G maps to NM_004210.4 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr17:7225204 C>T maps to NM_032442.2 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr17:7226378 C>A maps to NM_032442.2 A827A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr17:7222371 G>C maps to NM_032442.2 L1227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:7230257 C>T maps to NM_032442.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr17:7230209 G>A maps to NM_032442.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr17:7224100 G>A maps to NM_032442.2 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr17:7221240 G>A maps to NM_032442.2 F1357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr2:182543032 C>T maps to NM_002500.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr2:182543080 A>T maps to NM_002500.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr2:182543224 T>C maps to NM_002500.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:31378711 C>T maps to NM_022728.2 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr17:29483131 T>C maps to NM_001042492.2 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr17:29670103 C>G maps to NM_001042492.2 L2380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr17:29552111 G>T did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr17:29557314 C>T maps to NM_001042492.2 Q1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:29679407 C>T maps to NM_001042492.2 Q2531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr17:29554249 C>T maps to NM_001042492.2 Q756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:29490349 C>T maps to NM_001042492.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:29508735 G>A maps to NM_001042492.2 W221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:29541483 G>T maps to NM_001042492.2 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr17:29679317 G>T maps to NM_001042492.2 E2501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr17:29559125 C>A maps to NM_001042492.2 S1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr17:29676237 A>G maps to NM_001042492.2 E2430E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr17:29557903 C>G maps to NM_001042492.2 S1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr17:29665072 A>G maps to NM_001042492.2 Q2245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr17:29527519 C>T maps to NM_001042492.2 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr17:29559840 C>A maps to NM_001042492.2 V1146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr17:29663712 G>T maps to NM_001042492.2 E2070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr17:29562678 C>T maps to NM_001042492.2 L1253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr17:29554249 C>T maps to NM_001042492.2 Q756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr17:29684008 C>T maps to NM_001042492.2 H2590H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr17:29576047 C>T maps to NM_001042492.2 Q1341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr22:30067900 G>A maps to NM_181832.2 Q362Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr22:30051645 G>T maps to NM_181832.2 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr22:30057256 G>T maps to NM_181832.2 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr22:30054228 C>T maps to NM_181832.2 Y217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr22:30090751 G>A maps to NM_000268.3 Q583Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr22:30064419 G>A maps to NM_181832.2 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr1:204943841 C>T maps to ENST00000367172 N483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr1:204951128 C>T maps to ENST00000367172 I817I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr1:204955231 C>T maps to ENST00000367172 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:204985456 G>A maps to ENST00000367172 L1278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr1:204939814 C>T maps to ENST00000367172 R359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:204956660 T>C maps to ENST00000367172 Y969Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr1:204955123 C>T maps to ENST00000367172 L891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:204985480 C>T maps to ENST00000367172 D1286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr1:204944531 C>G maps to ENST00000367172 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr1:204956555 C>T maps to ENST00000367172 A934A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:69687307 C>T maps to NM_138713.2 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr16:69726487 G>A maps to NM_138713.2 Q920Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr16:69726421 G>A maps to NM_138713.2 Q898Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr18:77211715 G>A maps to NM_172387.1 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr18:77246359 G>A maps to NM_172387.1 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr20:50158936 G>A maps to NM_012340.3 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr20:50049279 C>T maps to NM_012340.3 K682K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:50051745 G>A maps to NM_012340.3 Q671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr20:50139825 G>A maps to NM_012340.3 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr20:50049189 C>G maps to NM_012340.3 P712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr20:50140649 C>T did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr20:50048712 G>A maps to NM_012340.3 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr20:50092155 G>A maps to NM_012340.3 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr20:50133355 G>A maps to NM_012340.3 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr20:50051830 G>A maps to NM_012340.3 I642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr20:50051779 G>A maps to NM_012340.3 Y659Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:28975090 C>G maps to NM_032815.3 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:28967612 C>T maps to NM_032815.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr16:28967367 C>A maps to NM_032815.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:68156559 G>A maps to NM_173165.2 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:68200794 C>T maps to NM_173165.2 R551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr16:68255130 C>T maps to NM_173163.2 Q1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr16:68215388 C>T maps to NM_173165.2 Q643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr14:24836319 C>T maps to NM_001136022.1 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr14:24841686 C>T maps to NM_001136022.1 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr12:54686941 G>C maps to NM_001136023.1 S113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr17:46136933 C>T maps to ENST00000362042 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr17:46135694 C>T maps to ENST00000362042 Y356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr7:26225054 C>A maps to NM_004289.6 I579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr7:26217661 C>T maps to NM_004289.6 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:14313492 G>A maps to ENST00000397581 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:3382104 G>A maps to ENST00000269778 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr19:3381828 G>T maps to ENST00000269778 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr9:94172989 G>A maps to NM_005384.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr9:94172287 G>A maps to NM_005384.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr19:13135863 G>A maps to ENST00000397661 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr19:13189482 C>T maps to ENST00000397661 Q338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:103505858 T>G maps to NM_003998.3 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr10:104160054 G>C maps to NM_001077494.1 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr10:104157413 A>G maps to NM_001077494.1 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr10:104157317 A>G maps to NM_001077494.1 K179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr10:104157341 G>C maps to NM_001077494.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:39399437 C>G maps to NM_002503.3 S346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr19:39398112 G>C maps to NM_002503.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr6:44233272 C>T maps to NM_004556.2 W76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr6:44227995 C>T maps to NM_004556.2 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:44232768 C>G maps to NM_004556.2 L244L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G2-A3IE-01A-11D-A20D-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-ZF-A9R0-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:145659459 G>A maps to NM_013432.4 T1096T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr8:145657805 G>A maps to NM_013432.4 N1199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr8:145665841 C>T maps to NM_013432.4 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr8:145660257 C>T maps to NM_013432.4 V1007V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr8:145667656 G>A maps to NM_013432.4 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr8:145666127 C>G maps to NM_013432.4 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr3:101574679 G>A maps to NM_031419.3 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr3:101578175 G>A maps to NM_031419.3 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr3:101573904 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:129744721 G>A maps to NM_006165.3 I673I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:34262519 G>C maps to NM_021100.4 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr9:33318946 C>T maps to NM_002504.4 C576C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr4:47901396 G>T maps to NM_152995.4 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr4:47905298 G>C maps to NM_152995.4 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:41057403 C>T maps to NM_002505.4 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr6:41059367 C>T maps to NM_002505.4 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:41215313 C>T maps to ENST00000308733 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr1:41218875 C>T maps to ENST00000308733 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:41236498 G>A maps to ENST00000308733 *459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr14:23938933 C>T maps to NM_001042635.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr2:233748752 G>C maps to NM_019850.2 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr1:115829230 G>A maps to NM_002506.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:115828702 C>T maps to NM_002506.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:47590073 C>G maps to NM_002507.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:47590091 C>G maps to NM_002507.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr17:47587922 C>T maps to NM_002507.3 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr23:102632753 G>T did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:102632602 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr3:25805629 G>C maps to NM_018297.3 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:25773929 C>T maps to NM_018297.3 Q435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr3:25820066 C>A maps to NM_018297.3 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr4:103822350 G>A maps to NM_139173.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr4:103827758 G>A maps to NM_139173.3 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr2:220022267 G>A maps to NM_024782.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:18122785 C>A maps to NM_198586.2 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr6:18122764 C>A maps to NM_198586.2 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr6:18122075 A>G maps to NM_198586.2 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:18122647 G>A maps to NM_198586.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr10:115664741 C>A maps to NM_198514.3 S624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:39621937 C>T maps to NM_001012754.2 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr13:39621832 T>C maps to NM_001012754.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr13:39613331 G>T maps to NM_001012754.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr23:17744786 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:17749979 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:17744063 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:17750027 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr23:17745287 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr23:17744474 G>T did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr23:17746217 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr23:17750459 G>C did not map to a codon.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr23:17744281 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr23:17744899 C>G did not map to a codon.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr23:17744538 G>A did not map to a codon.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr23:17745226 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr23:17739624 A>G did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:17745890 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr23:17746328 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr23:17750301 G>A did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:71360361 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr3:49466642 C>T maps to NM_032316.3 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr1:236205405 G>A maps to NM_002508.2 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:236228223 G>A maps to NM_002508.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:236205224 C>A maps to NM_002508.2 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:236180523 G>A maps to NM_002508.2 I726I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr1:236148685 A>G maps to NM_002508.2 I1016I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr1:236180535 C>T maps to NM_002508.2 G722G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:236189247 C>T maps to NM_002508.2 Q644Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr14:52496265 C>G maps to NM_007361.3 V800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr14:52474663 C>T maps to NM_007361.3 W1248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr14:52477649 G>A maps to NM_007361.3 V1222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr14:52535545 G>T maps to NM_007361.3 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:201757013 T>A maps to NM_001136039.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:201760083 C>T maps to NM_001136039.2 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr14:51190284 C>A maps to NM_020921.3 E2100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:51196369 C>T maps to NM_020921.3 Q1983Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:51204914 C>T maps to NM_020921.3 L1906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr14:51288735 G>C maps to NM_020921.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr14:51259485 C>A maps to NM_020921.3 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr14:51243771 C>T maps to NM_020921.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr14:51224626 C>A maps to NM_020921.3 E1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr14:51190224 G>A maps to NM_020921.3 L2120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr14:51223274 C>A maps to NM_020921.3 L1491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:674517 G>A maps to NM_016533.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr20:25443044 C>A maps to NM_025176.4 E1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr20:25456692 C>T maps to NM_025176.4 L1078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr20:25472001 C>T maps to NM_025176.4 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr16:69375533 G>A maps to NM_016101.4 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr16:69373924 C>T maps to NM_016101.4 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr15:23019853 G>A maps to NM_030922.6 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr15:23019801 G>C maps to NM_030922.6 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:99234790 C>A maps to NM_024759.1 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:24768669 C>T maps to NM_020448.4 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:24768669 C>T maps to NM_020448.4 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:24779977 C>G maps to NM_020448.4 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr5:156890298 A>T maps to NM_001099287.1 K141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr5:36995748 A>G maps to NM_133433.3 K1049K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr5:37024739 T>C maps to NM_133433.3 C1876C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr5:36985879 A>G maps to NM_133433.3 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:37045559 T>A maps to NM_133433.3 L2120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:36953854 C>T maps to NM_133433.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:37019410 A>T did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:37064930 G>A maps to NM_133433.3 L2784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:37059267 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:36984857 C>T maps to NM_133433.3 Q526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr22:29965260 G>A maps to NM_003634.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr22:29957497 G>C maps to NM_003634.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr22:29966487 G>A maps to NM_003634.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr22:29966392 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr22:29957497 G>C maps to NM_003634.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr3:52491870 C>T maps to NM_007184.3 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:161089362 C>T maps to NM_005600.2 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:161088992 G>T maps to NM_005600.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr6:125139600 C>T maps to NM_001040214.1 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr20:61880214 C>T maps to NM_152864.3 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:119077192 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr23:119063989 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr23:119059250 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:119077326 C>G did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:119059242 C>T did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:119059248 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:119059258 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:119059225 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:28228102 C>A maps to NM_001007531.1 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:28227838 G>A maps to NM_001007531.1 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr6:28227298 C>A maps to NM_001007531.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr16:50667469 C>G maps to NM_033119.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:1036491 C>T maps to NM_033120.2 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:51875519 G>A maps to NM_005601.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr19:51875192 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr19:51875233 G>A maps to NM_005601.3 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr17:40174612 G>T maps to ENST00000316082 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr17:40174450 C>T maps to ENST00000316082 Y43Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:45655521 G>A maps to NM_198478.3 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr19:45655297 G>T maps to NM_198478.3 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr19:45655624 G>C maps to NM_198478.3 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr19:45656275 G>C maps to NM_198478.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr23:118723318 T>C did not map to a codon.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr23:118724535 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr23:118723634 G>T did not map to a codon.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr23:118726372 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr23:118723503 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:118724733 A>G did not map to a codon.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr23:118725221 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr3:42678912 C>T maps to NM_005385.3 Q573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:42679095 C>T maps to NM_005385.3 Q634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr3:42659088 C>G maps to NM_005385.3 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:42687460 C>T maps to NM_005385.3 Y1461Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr3:42680096 G>A maps to NM_005385.3 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr14:36987030 C>A maps to NM_001079668.2 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:21492921 G>T maps to NM_002509.2 S154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr20:21494289 T>C maps to NM_002509.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr20:21492641 G>T maps to NM_002509.2 Y247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr20:21494154 G>T maps to NM_002509.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr10:101294754 G>A maps to NM_145285.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr20:21376857 C>T maps to NM_033176.1 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr5:172660108 C>T maps to NM_004387.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr5:172659845 G>T maps to NM_004387.3 S234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:13543784 C>T maps to NM_001189.3 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:33463471 G>A maps to NM_018096.3 N291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr17:33469021 G>A maps to NM_018096.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr3:173998672 A>G maps to NM_014932.2 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr17:7318913 C>G maps to NM_020795.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:7319381 C>G maps to NM_020795.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr17:7318928 C>G maps to NM_020795.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr23:70387241 C>G did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr23:70387458 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr23:70387300 G>C did not map to a codon.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr23:70367905 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr23:70387128 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:70367744 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:70367797 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:70368013 G>A did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:5827105 T>C did not map to a codon.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr23:6069449 T>A did not map to a codon.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr23:5821763 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:5821674 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr24:16835001 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr24:16734318 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr5:65084302 C>T maps to NM_020726.4 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr5:65118646 G>A maps to NM_020726.4 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr16:3598710 G>A maps to ENST00000448023 I928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr16:3613704 C>T maps to ENST00000448023 K458K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:3604253 G>A maps to ENST00000448023 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:32461379 C>A maps to NM_021209.4 L850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr2:32474973 G>A maps to NM_021209.4 F653F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:32476323 G>A maps to NM_021209.4 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr2:32475993 C>G maps to NM_021209.4 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr2:32449684 G>A maps to NM_021209.4 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr2:32475392 G>A maps to NM_021209.4 Q514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr16:57062285 G>A maps to NM_032206.3 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr16:57062058 G>A maps to NM_032206.3 Q717Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr16:57065330 C>T maps to NM_032206.3 I811I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:57085521 G>A maps to NM_032206.3 L1165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr16:57115510 C>T maps to NM_032206.3 I1826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr16:57089389 C>T maps to NM_032206.3 L1235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:57080544 G>A maps to NM_032206.3 R1110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr16:57054677 G>C maps to NM_032206.3 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr16:57073701 C>T maps to NM_032206.3 H937H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:57060527 C>G maps to NM_032206.3 S558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:5462821 G>A maps to NM_033004.3 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:5418328 C>T maps to NM_033004.3 L1389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr17:5445292 C>T maps to NM_033004.3 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:5462749 C>T maps to NM_033004.3 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr11:7981265 T>G maps to NM_176821.3 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:7984931 C>T maps to NM_176821.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr11:7982291 G>A maps to NM_176821.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr19:54327326 G>A maps to ENST00000391773 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:54313766 C>T maps to ENST00000391773 E382E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr19:54313189 G>A maps to ENST00000391773 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr19:54314477 C>A maps to ENST00000391773 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:54304578 C>G maps to ENST00000391773 L887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:54313925 C>T maps to ENST00000391773 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr19:54304647 C>T maps to ENST00000391773 L864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:54327329 C>T maps to ENST00000391773 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr19:56423784 T>A maps to NM_176810.2 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr19:56407331 G>A maps to NM_176810.2 C1037C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr19:56419204 C>T maps to NM_176810.2 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr19:56436333 T>A maps to NM_176810.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:56413510 C>T maps to NM_176810.2 Q893Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr19:56407430 G>C maps to NM_176810.2 L1004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr19:56443614 C>T maps to NM_176810.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr19:56423178 G>A maps to NM_176810.2 D668D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr19:56407403 C>G maps to NM_176810.2 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:7064320 C>G maps to NM_176822.3 S355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr11:7064874 C>T maps to NM_176822.3 R540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr11:7064528 G>A maps to NM_176822.3 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr11:7064537 G>T maps to NM_176822.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:7064451 C>T maps to NM_176822.3 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr11:7064633 T>C maps to NM_176822.3 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr19:55493696 C>T maps to NM_017852.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:55494634 G>A maps to NM_017852.3 E523E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr19:55493758 A>G maps to NM_017852.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:55508801 G>A maps to NM_017852.3 V999V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr19:55493812 G>A maps to NM_017852.3 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr19:55494385 C>T maps to NM_017852.3 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr19:55494472 T>C maps to NM_017852.3 D469D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:247587252 C>T maps to NM_004895.4 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr1:247587653 C>A maps to NM_004895.4 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr1:247607345 C>G maps to NM_004895.4 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr1:247582263 G>T maps to NM_004895.4 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:247587617 G>A maps to NM_004895.4 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:247588548 C>T maps to NM_004895.4 Q602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr1:247599341 C>T maps to NM_004895.4 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:247592973 C>A maps to NM_004895.4 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr19:56373456 C>G maps to NM_134444.4 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr19:56369551 C>T maps to NM_134444.4 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr19:56382201 C>T maps to NM_134444.4 F788F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:56388433 G>A maps to NM_134444.4 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr19:56388415 C>A maps to NM_134444.4 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr19:56552341 C>T maps to NM_153447.4 L947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr19:56515150 G>A maps to NM_153447.4 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr19:56552341 C>T maps to NM_153447.4 L947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr19:56572821 C>G maps to NM_153447.4 L1177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:56538993 C>T maps to NM_153447.4 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr19:56539146 C>T maps to NM_153447.4 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr19:56544985 C>G maps to NM_153447.4 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:56538740 G>A maps to NM_153447.4 W381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr19:55451127 G>A maps to ENST00000446217 N381N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr19:55450779 G>A maps to ENST00000446217 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:55453051 G>A maps to ENST00000446217 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr19:55445984 G>A maps to ENST00000446217 F809F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr19:55449551 G>C maps to ENST00000446217 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr19:56467115 C>T maps to NM_176811.2 N564N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:56466731 C>T maps to NM_176811.2 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr19:56466504 G>T maps to NM_176811.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:56466275 C>G maps to NM_176811.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr19:56466275 C>T maps to NM_176811.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr19:56466878 C>A maps to NM_176811.2 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:56466176 G>A maps to NM_176811.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr19:56466476 C>T maps to NM_176811.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr19:56466329 G>A maps to NM_176811.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:56466416 G>A maps to NM_176811.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr19:56244155 C>T maps to NM_176820.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:56228107 G>A maps to NM_176820.2 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr19:56226545 G>T maps to NM_176820.2 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr19:56244842 G>A maps to NM_176820.2 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:56241198 G>A maps to NM_176820.2 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr11:119045439 C>T maps to NM_024618.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr11:119050747 C>A maps to NM_024618.2 S673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr11:119044680 C>A maps to NM_024618.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr11:119044704 C>G maps to NM_024618.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:119044704 C>G maps to NM_024618.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr11:119051888 C>T maps to NM_024618.2 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr11:119044626 G>A maps to NM_024618.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr15:85200430 G>A maps to NM_205858.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7N-01A-11D-A391-08 chr6:142409681 C>T maps to NM_002511.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr3:160942824 C>A maps to ENST00000472947 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:49233089 C>T maps to ENST00000393198 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr17:49231767 C>T maps to ENST00000393198 Q12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr16:449377 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:169206873 G>C maps to NM_013330.3 S269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:152127233 T>C maps to NM_004688.2 Q299Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr2:152127334 G>A maps to NM_004688.2 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr2:152132273 G>A maps to NM_004688.2 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:10032142 C>T maps to NM_022787.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr1:183261926 G>T maps to NM_015039.2 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:183230153 G>C maps to NM_015039.2 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr16:4511812 C>A maps to NM_020677.3 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr16:4511852 C>T maps to NM_020677.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr17:43180479 C>T maps to NM_021079.3 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr10:15154864 G>C maps to ENST00000378143 S454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr4:56471507 A>C maps to NM_006681.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:232392924 G>A maps to NM_006056.4 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:151784386 G>T maps to NM_020167.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:114182805 G>A maps to NM_006169.2 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr5:43628316 A>G maps to NM_182977.2 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr5:43613175 T>C maps to NM_182977.2 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr16:69778784 G>A maps to NM_014062.1 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr16:69776285 C>T maps to NM_014062.1 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr16:69776431 G>A maps to NM_014062.1 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:144097328 C>T maps to ENST00000467773 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:883902 C>G maps to NM_015658.3 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:892339 C>T maps to NM_015658.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:880096 G>A maps to NM_015658.3 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:132632647 G>A maps to NM_024078.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr12:132635829 C>G maps to NM_024078.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:30492525 G>A maps to NM_006092.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr7:30496458 G>T maps to NM_006092.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr7:30490887 G>C maps to NM_006092.2 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr16:50745864 G>A maps to NM_022162.1 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:50745518 C>G maps to NM_022162.1 S566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr16:50759417 C>T maps to NM_022162.1 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr16:50745144 G>A maps to NM_022162.1 E441E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:50750867 G>A maps to NM_022162.1 Q871Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr16:50756556 C>T maps to NM_022162.1 D913D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr16:50733834 C>T maps to NM_022162.1 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr10:72201264 C>T maps to NM_018055.4 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr17:54671874 C>A maps to NM_005450.4 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr17:54671640 G>A maps to NM_005450.4 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr2:10712232 C>T maps to NM_024894.2 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr17:65714107 G>C maps to NM_015462.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr17:65733790 G>A maps to NM_015462.3 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:65734346 C>T maps to NM_015462.3 Q547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr22:38084980 C>A maps to NM_024313.2 L121L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CF-A9FF-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:67208572 G>A maps to ENST00000432069 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr18:31463351 C>A maps to NM_003787.4 E527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr18:31538214 C>T maps to NM_003787.4 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:31432904 G>T maps to NM_003787.4 I606I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr18:31463385 A>G maps to NM_003787.4 D515D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr9:33464904 G>C maps to NM_022917.4 L917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr9:33468849 C>A maps to NM_022917.4 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr9:33466614 C>T maps to NM_022917.4 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr9:33468518 G>C maps to NM_022917.4 S398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr9:33469524 C>T maps to NM_022917.4 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:13620484 G>C maps to NM_016167.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr9:95076683 A>G maps to NM_017948.5 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr1:6585955 C>T maps to NM_024654.4 E689E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:6614475 G>C maps to NM_024654.4 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr10:103920636 A>T maps to ENST00000405356 K520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr7:156746907 C>T maps to NM_138400.1 C408C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr7:156743088 C>T maps to NM_138400.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:14947421 G>A maps to ENST00000456867 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:14962406 A>G maps to ENST00000456867 E603E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr16:14973933 G>A maps to ENST00000456867 Q940Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr16:18544482 C>G maps to NM_001004060.1 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:18549882 C>T maps to NM_001004060.1 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:16349967 C>T maps to ENST00000263012 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:70514146 G>T did not map to a codon.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr23:70514378 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr23:70517695 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr23:70517718 G>A did not map to a codon.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr23:70510514 G>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr4:2940929 G>C maps to NM_003703.1 S820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr4:2951771 C>A maps to NM_003703.1 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:2951721 C>T maps to NM_003703.1 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr5:175812328 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:6675397 C>A maps to ENST00000382421 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr12:6670222 C>T maps to ENST00000382421 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr12:6666704 C>T maps to ENST00000382421 K664K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:6670228 C>T maps to ENST00000382421 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr20:2633519 C>G maps to NM_006392.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:2636003 G>A maps to NM_006392.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr20:2637103 C>T maps to NM_006392.2 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr20:2638759 G>A maps to NM_006392.2 K535K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr12:117662914 G>A maps to ENST00000338101 N1278N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr12:117696869 G>T maps to ENST00000338101 T811T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:117724010 A>G maps to ENST00000338101 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr12:117698414 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr12:117662862 G>A maps to ENST00000338101 R1296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr12:117728212 G>A maps to ENST00000338101 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr12:117723944 C>T maps to ENST00000338101 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:162337158 G>T maps to NM_014697.2 E475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr1:162325124 C>G maps to NM_014697.2 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr17:26106003 G>T maps to NM_000625.4 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr17:26108094 G>A maps to NM_000625.4 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr17:26086023 G>C maps to NM_000625.4 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr17:26086098 G>C maps to NM_000625.4 V1054V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:26114738 G>A maps to NM_000625.4 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr7:150696093 C>T maps to NM_000603.4 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:150709516 C>T maps to NM_000603.4 F1021F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr7:150707368 C>T maps to NM_000603.4 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr7:150707854 G>A maps to NM_000603.4 E952E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr7:150711255 G>A maps to NM_000603.4 *1204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr7:150696313 C>T maps to NM_000603.4 Y331Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr19:50059585 G>A maps to NM_015953.3 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr19:50059897 G>A maps to NM_015953.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:169699575 G>A maps to NM_001171631.1 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr2:169681197 G>A maps to NM_001171631.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr9:139391497 G>C maps to NM_017617.3 L2231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr9:139395036 C>T maps to NM_017617.3 A1967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr9:139405105 G>A maps to NM_017617.3 P913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr9:139399555 G>A maps to NM_017617.3 N1529N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr9:139418226 G>A maps to NM_017617.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr9:139405622 G>C maps to NM_017617.3 V856V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr9:139391743 G>C maps to NM_017617.3 L2149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr9:139393595 G>C maps to NM_017617.3 S2017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr9:139395121 G>C maps to NM_017617.3 S1939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr9:139410067 G>C maps to NM_017617.3 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:120539857 G>A maps to NM_024408.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr1:120510123 G>C maps to NM_024408.2 S462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:120461053 C>T maps to NM_024408.2 A1968A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:120539791 C>T maps to NM_024408.2 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:120539833 A>G maps to NM_024408.2 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:120548018 C>T maps to NM_024408.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:120466573 G>A maps to NM_024408.2 D1515D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:145273376 G>C maps to ENST00000454606 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr1:145281696 C>T maps to ENST00000454606 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr19:15278172 C>T maps to NM_000435.2 W1750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr19:15297740 G>C maps to NM_000435.2 V633V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr6:32169123 C>A maps to NM_004557.3 L1303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr6:32164179 C>T maps to NM_004557.3 W1740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:32164148 G>A maps to NM_004557.3 A1750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:32170229 C>T maps to NM_004557.3 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr6:32164699 A>G did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:79918539 C>T maps to NM_178493.5 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:79911121 C>T maps to NM_178493.5 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:79916821 G>A maps to NM_178493.5 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr8:120428804 C>T maps to NM_002514.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:27064679 A>G maps to ENST00000449198 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr14:26918046 G>A maps to ENST00000449198 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:46443273 G>A maps to NM_002516.2 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr19:46443267 C>T maps to NM_002516.2 K444K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr23:100105212 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr23:100125720 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr23:100118474 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:100105236 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:100105270 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:89224387 G>A maps to NM_016931.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr11:89133384 G>A maps to NM_016931.3 Q337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr11:89184973 A>G maps to NM_016931.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:89133451 G>A maps to NM_016931.3 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr11:89224387 G>A maps to NM_016931.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr11:89133466 G>A maps to NM_016931.3 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr15:69339793 C>A maps to NM_024505.3 I578I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr15:69327744 C>T maps to NM_024505.3 Q303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:69327704 C>T maps to NM_024505.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr15:69328164 C>T maps to NM_024505.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr9:140327506 A>G maps to NM_006647.1 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr16:2029283 C>G maps to NM_172168.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:47535975 C>T maps to NM_002517.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr19:47548575 C>T maps to NM_002517.2 D480D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:101580598 C>T maps to NM_002518.3 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:101554279 C>T maps to NM_002518.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr2:101598811 C>T maps to NM_002518.3 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr2:101594222 C>T maps to NM_002518.3 Q482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:101584863 C>T maps to NM_002518.3 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr2:101611914 C>T maps to NM_002518.3 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr2:101606887 C>T maps to NM_002518.3 F666F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:34270182 C>T maps to NM_001164749.1 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr11:66189920 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:66192479 G>T maps to NM_178864.3 E707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr11:66190263 G>T maps to NM_178864.3 G184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr11:66191515 T>C maps to NM_178864.3 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr11:108043490 G>C maps to NM_002519.2 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr11:108062879 T>C maps to NM_002519.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:53853102 C>T maps to NM_005285.3 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr8:53853372 C>T maps to NM_005285.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr8:53853372 C>T maps to NM_005285.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr8:53852721 C>G maps to NM_005285.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr18:21148962 C>T did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr18:21120456 C>G maps to NM_000271.4 L853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr18:21148934 C>T maps to NM_000271.4 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr18:21148903 G>A maps to NM_000271.4 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr18:21119388 G>A maps to NM_000271.4 F947F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr18:21114523 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr18:21128073 T>C did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr7:44579101 G>A maps to NM_013389.2 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:44561679 C>T maps to NM_013389.2 K933K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr7:44555495 G>A maps to NM_013389.2 L1261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr7:44556400 G>C maps to NM_013389.2 L1167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr7:44560682 G>T maps to NM_013389.2 I996I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr7:44555564 C>T did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr7:44560691 G>A maps to NM_013389.2 C993C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr7:44560709 C>T maps to NM_013389.2 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:139937505 C>T maps to ENST00000371600 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:45669323 C>T maps to NM_006310.3 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr4:73013406 C>T maps to NM_004885.2 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:73012821 G>T maps to NM_004885.2 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr4:72994448 C>T maps to NM_004885.2 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr3:132418267 C>T maps to ENST00000393156 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:132418249 C>T maps to ENST00000393156 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr3:132409475 C>T maps to ENST00000393156 W863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:132405183 A>T maps to ENST00000393156 L1083L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr3:132440814 C>A maps to ENST00000393156 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr1:5924051 G>A maps to NM_015102.2 V1346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr1:6008251 G>A maps to NM_015102.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr1:6027389 G>C maps to NM_015102.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr1:5947409 G>A maps to NM_015102.2 R807R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:6021917 A>C maps to NM_015102.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:5940234 G>A maps to NM_015102.2 I850I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr1:5934638 G>A maps to NM_015102.2 F1041F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:36322259 G>T maps to NM_004646.3 R1109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:36322009 C>T maps to NM_004646.3 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:36339655 C>T maps to NM_004646.3 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr19:36339251 C>T maps to NM_004646.3 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr19:36333174 G>C maps to NM_004646.3 P838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr19:36342421 G>A maps to NM_004646.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr19:36340482 G>C maps to NM_004646.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:179526244 G>A maps to NM_014625.2 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:179526362 G>A maps to NM_014625.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:179520418 C>T maps to NM_014625.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr16:15045812 C>G maps to NM_006985.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr17:79580441 G>A maps to NM_017921.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr17:79589208 G>C maps to NM_017921.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr5:170814951 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr4:106861307 C>T maps to ENST00000503451 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr1:11907621 G>A maps to NM_006172.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr1:153652192 G>T maps to NM_000906.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr1:153653073 G>C maps to NM_000906.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr1:153652174 C>T maps to NM_000906.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr9:35792662 C>T maps to NM_003995.3 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr9:35805554 C>G maps to NM_003995.3 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:35808546 C>A maps to NM_003995.3 L918L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:35792644 A>G maps to NM_003995.3 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr9:35792992 C>T maps to NM_003995.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr9:35801945 C>A maps to NM_003995.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr5:32712403 C>G maps to ENST00000265074 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr5:32712274 C>A maps to ENST00000265074 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr5:32739135 C>T maps to ENST00000265074 Y353Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:34874017 C>T maps to NM_207172.1 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr7:34698053 C>T maps to NM_207172.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr15:73862584 G>C maps to NM_012428.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr15:73862521 C>T maps to NM_012428.3 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr15:73889660 G>T maps to NM_012428.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr17:78444648 G>T maps to NM_002522.3 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr17:78449359 G>T maps to NM_002522.3 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr17:78447206 G>A maps to NM_002522.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:78444774 G>A maps to NM_002522.3 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr7:98256481 G>T maps to NM_002523.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:98256631 C>T maps to NM_002523.2 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr22:39218742 G>A maps to NM_014293.2 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr22:39224454 G>T maps to NM_014293.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr7:25264764 A>G maps to NM_022150.3 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr4:164246738 G>A maps to NM_000909.4 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr4:164247288 G>A maps to NM_000909.4 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr4:164247452 G>C maps to NM_000909.4 S85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr4:164247253 A>G maps to NM_000909.4 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr4:156136152 C>A maps to NM_000910.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr4:156136029 C>T maps to NM_000910.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr4:156135696 C>T maps to NM_000910.2 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr4:156135648 C>T maps to NM_000910.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr4:164272306 A>G maps to NM_006174.2 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr23:30327165 C>G did not map to a codon.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr23:30327118 G>C did not map to a codon.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr23:30327071 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:30322791 G>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr17:38249334 G>T maps to NM_003250.5 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr17:38253436 G>C maps to NM_021724.3 S84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr3:24018853 C>T maps to NM_005126.4 R562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr19:50881883 C>A maps to NM_007121.4 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:50881972 C>T maps to NM_007121.4 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr19:50881475 C>T maps to NM_007121.4 H84H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr11:47282942 C>T maps to NM_005693.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr11:47282063 C>T maps to NM_005693.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr12:100904718 C>A maps to ENST00000392986 Y81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr3:119528934 G>C maps to NM_022002.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr3:119529018 G>A maps to NM_022002.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr3:119528973 G>A maps to NM_022002.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr3:119534284 A>G maps to NM_022002.2 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr3:119535947 C>T maps to NM_022002.2 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:161203027 C>T maps to NM_001077482.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:161203048 C>T maps to NM_001077482.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr12:95434301 C>A maps to NM_003297.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr12:95419031 C>G did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr3:15073964 C>G maps to NM_003298.3 S416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr3:15045490 C>T maps to NM_003298.3 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:108496092 G>A maps to ENST00000368983 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr6:108496044 C>G maps to ENST00000368983 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr5:92923968 G>A maps to NM_005654.4 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr15:96875687 C>T maps to NM_021005.3 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr15:96880629 C>T maps to NM_021005.3 Q342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:17343274 G>A maps to NM_005234.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr19:17351552 G>A maps to NM_005234.3 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:142680254 A>G maps to NM_001024094.1 N515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr4:149073666 A>G maps to ENST00000511528 H825H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr4:149356371 C>G maps to ENST00000511528 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr4:149181139 T>C maps to ENST00000511528 R629R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr2:157182447 G>C maps to NM_006186.3 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr2:157183309 G>A maps to NM_006186.3 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:157184434 C>T maps to NM_006186.3 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:157182438 G>A maps to NM_006186.3 H538H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr9:102590461 G>A maps to NM_173200.1 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr9:102590790 G>A maps to NM_173200.1 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:200017816 G>A maps to NM_205860.1 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:200014629 C>T maps to NM_205860.1 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr9:127285046 C>T maps to NM_033334.2 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:127289099 C>A maps to NM_033334.2 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr10:115374001 C>T maps to ENST00000369358 R1088R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr10:115350588 G>A maps to ENST00000369358 V1576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr10:115365555 G>A maps to ENST00000369358 Q1302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr10:115401141 A>G maps to ENST00000369358 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr10:115350618 G>A maps to ENST00000369358 D1566D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr10:115380419 G>C maps to ENST00000369358 V947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr10:115364601 G>A maps to ENST00000369358 I1339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr9:140196036 C>T maps to NM_001004354.2 *115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr9:140196071 G>A maps to NM_001004354.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr1:115252335 G>A maps to NM_002524.3 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr10:64911925 C>G maps to NM_030759.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:64913494 G>T maps to NM_030759.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:27664001 G>A maps to ENST00000379863 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr8:144920869 C>G maps to NM_178564.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr8:144919308 G>A maps to NM_178564.3 R389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr7:107847974 C>A maps to ENST00000379032 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr7:107872809 G>A maps to ENST00000379032 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr7:107822276 G>A maps to ENST00000379032 Q879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr1:52277749 C>T maps to NM_002525.2 V633V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr1:52344113 A>G maps to NM_002525.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:52344257 G>A maps to NM_002525.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr7:129394930 G>A maps to ENST00000393231 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr7:129394930 G>A maps to ENST00000393231 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr7:129348982 G>C maps to ENST00000393231 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr8:32599592 A>T maps to ENST00000338921 K234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr8:32600274 C>T maps to NM_013958.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr8:32505448 C>G maps to NM_013959.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr8:31498062 G>A maps to NM_013962.2 W188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr8:32620828 C>A maps to NM_001160004.1 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:84733645 G>T maps to ENST00000404547 G463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr10:84745171 C>A maps to ENST00000404547 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr15:76301590 C>G maps to NM_138573.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr21:16338391 C>A maps to NM_003489.3 E708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr21:16340219 C>T maps to NM_003489.3 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr21:16339705 G>A maps to NM_003489.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr21:16339589 G>T maps to NM_003489.3 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr21:16340309 G>A maps to NM_003489.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr21:16337171 C>T maps to NM_003489.3 T1114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr21:16337171 C>T maps to NM_003489.3 T1114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:105193616 G>T did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr23:105178384 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr23:105153493 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:105153031 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:105159727 G>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr6:30658706 G>A maps to NM_007243.1 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:30656614 C>T maps to NM_007243.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr6:5999355 C>T maps to NM_016588.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:67919691 C>T maps to NM_198443.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr16:67919745 G>A maps to NM_198443.1 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr10:33510784 G>A maps to NM_003873.5 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr10:33619688 C>T maps to NM_003873.5 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr2:206590656 C>T maps to NM_201266.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr2:206581042 C>T maps to NM_201266.1 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr2:206605262 T>C maps to NM_201266.1 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr2:206588551 T>A maps to NM_201266.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr20:334237 C>T maps to NM_024958.2 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr2:51254931 C>T maps to ENST00000404971 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:50850595 A>G maps to ENST00000404971 Y363Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:51254844 G>A maps to ENST00000404971 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr2:50724723 C>A maps to ENST00000404971 G916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:50779930 A>C maps to ENST00000404971 L558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:51253542 G>T maps to ENST00000404971 Y279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr2:50780088 G>T maps to ENST00000404971 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr2:50463994 G>A maps to ENST00000404971 Q1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:50779935 G>C maps to ENST00000404971 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:50149200 G>A maps to ENST00000404971 R1509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:50280645 G>A maps to ENST00000404971 L1337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr11:64418926 G>A maps to NM_015080.3 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr11:64374862 G>T maps to NM_015080.3 L1648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr11:64428407 G>A maps to NM_015080.3 R668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr11:64427939 C>T maps to NM_015080.3 T751T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr11:64480979 C>A maps to NM_015080.3 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:64410026 G>A maps to NM_138734.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:64457928 G>A maps to NM_015080.3 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr14:79432494 T>C maps to NM_004796.4 N468N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:79270146 C>G maps to NM_004796.4 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr14:80328210 C>A maps to NM_004796.4 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr14:79117669 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr14:79175876 C>T maps to NM_004796.4 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr5:74069826 C>T maps to NM_014886.3 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr5:176721871 G>T maps to NM_022455.4 P2501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:176721472 C>G maps to NM_022455.4 A2368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:176637916 G>A maps to NM_022455.4 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr5:176666835 C>G maps to NM_022455.4 P1424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr5:176562541 C>T maps to NM_022455.4 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr23:152014894 G>A did not map to a codon.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr23:152031184 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:152034464 A>G did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr17:44788429 G>A maps to NM_006178.2 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr20:1433190 C>A maps to ENST00000476071 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:1426393 G>A maps to ENST00000476071 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr20:1424400 A>C maps to ENST00000476071 L371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:1447414 C>A maps to ENST00000476071 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:212911827 C>T maps to NM_015471.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr8:59502624 C>T maps to NM_001144772.1 S707S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:59555591 C>A maps to NM_001144772.1 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr8:59522162 C>T maps to NM_001144772.1 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr8:59506849 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr8:59522182 G>A maps to NM_001144772.1 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr8:59515823 G>C maps to NM_001144772.1 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr8:59511908 A>G maps to NM_001144772.1 F520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr8:59514697 T>C did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr16:27246540 C>T maps to NM_145080.3 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:27246531 G>A maps to NM_145080.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr8:126114643 C>G maps to NM_173685.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr8:126369554 T>A maps to NM_173685.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr5:6606937 A>C maps to NM_017755.5 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47W-01A-11D-A23U-08 chr5:6625782 C>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:6605469 C>T maps to NM_017755.5 R551R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr5:6604749 C>A maps to NM_017755.5 E596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr3:93802970 C>G maps to NM_022072.3 S48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:46827298 C>G maps to NM_199044.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:72721625 C>T maps to NM_148956.2 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr7:72717995 G>C maps to NM_148956.2 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr10:18840785 G>T maps to NM_182543.2 S346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr10:18903390 C>T maps to NM_182543.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr4:40800814 C>T maps to NM_024677.4 Q432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr4:40778147 C>G maps to NM_024677.4 S303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr4:40778195 C>G maps to NM_024677.4 S319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr4:40752968 C>T maps to NM_024677.4 Q87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:40129050 G>C maps to NM_032526.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:40137688 C>A maps to NM_032526.1 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr1:40129029 G>C maps to NM_032526.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr1:40131796 G>A maps to NM_032526.1 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr2:18765806 C>T maps to ENST00000455492 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr2:18765818 C>T maps to ENST00000455492 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr2:18757542 G>A maps to ENST00000455492 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr10:104865527 A>G maps to NM_001134373.1 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr10:104853780 C>T maps to NM_001134373.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:33066464 G>A maps to NM_001002010.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr6:116436851 A>G did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr3:52561906 C>G maps to NM_001134231.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr3:52558713 G>A maps to NM_001134231.1 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:52558486 C>T maps to NM_001134231.1 *558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:104190737 G>A maps to NM_001031701.2 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr12:104171813 G>A maps to NM_001031701.2 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr12:104187021 G>A maps to NM_001031701.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr6:86159925 G>A maps to NM_002526.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMJ-01A-11D-A42E-08 chr6:86181105 C>G maps to NM_002526.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:86176991 C>G maps to NM_002526.2 S185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:15133843 T>A maps to NM_173474.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr12:5603793 G>C maps to NM_001102654.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr16:2097806 C>G maps to NM_002528.5 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:2090034 C>A maps to NM_002528.5 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:132184469 G>A maps to NM_001144058.1 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr11:132081932 G>T maps to NM_001144058.1 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr11:132016232 C>G maps to NM_001144058.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr11:132082041 G>A did not map to a codon.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr11:132204946 C>T maps to NM_001144058.1 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr11:132184538 C>T maps to NM_001144058.1 N292N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr11:132016397 C>T maps to NM_001144058.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr17:9143221 G>A maps to NM_004822.2 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:96077359 C>T maps to NM_021229.3 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr12:96131820 C>T maps to NM_021229.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:107867235 G>A maps to NM_001113226.1 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:107937880 G>A maps to NM_001113226.1 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr9:135116295 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr1:156846340 C>T maps to NM_002529.3 H594H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:156845890 C>A maps to NM_002529.3 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr1:156845926 C>T maps to NM_002529.3 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:156843617 C>G maps to NM_002529.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:156843554 C>T maps to NM_002529.3 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr9:87570362 G>A maps to NM_006180.3 G701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:87285752 C>T maps to NM_006180.3 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr9:87366902 C>A maps to NM_006180.3 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr9:87338521 C>T maps to NM_006180.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr9:87342635 G>A maps to NM_006180.3 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr9:87317106 C>A maps to NM_006180.3 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:88679229 C>G maps to NM_001012338.1 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr15:88678347 G>A maps to NM_001012338.1 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr15:88576242 G>C maps to NM_001012338.1 S477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr15:88690603 G>C maps to NM_001012338.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr15:88799171 G>A maps to NM_001012338.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr15:88670428 G>A maps to NM_001012338.1 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr12:86268210 A>G maps to NM_006183.3 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr20:61386080 G>A maps to NM_002531.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr20:61391507 C>G maps to NM_002531.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:11802147 C>T maps to NM_012344.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:11798718 G>A maps to NM_012344.3 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:11809715 G>A maps to NM_012344.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr2:11802345 G>A maps to NM_012344.3 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr2:11802135 G>A maps to NM_012344.3 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:11800236 G>A maps to NM_012344.3 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr12:106461077 C>G maps to NM_014840.2 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr12:106460645 G>A maps to NM_014840.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr12:106466591 G>A maps to NM_014840.2 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:106460771 G>A maps to NM_014840.2 I598I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr1:205273536 G>A maps to ENST00000441520 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:205273339 C>T maps to ENST00000441520 K419K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr16:10850574 C>A maps to NM_002484.2 S130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr14:32031320 C>T maps to NM_025152.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:49425625 C>G maps to NM_006184.5 S444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr1:27272062 C>A maps to NM_006600.2 S277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:27269396 A>G maps to NM_006600.2 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr1:27267977 C>T maps to NM_006600.2 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr5:162884086 C>G did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr5:162881035 A>G maps to NM_145266.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr7:44524826 T>C maps to NM_015332.3 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr7:2284268 G>C maps to NM_198954.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:51075816 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr23:51075910 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr23:51239031 G>C did not map to a codon.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr23:51239168 T>C did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr10:74879773 A>C did not map to a codon.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr10:74890528 G>A maps to NM_015901.4 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr14:105644072 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:131102020 C>T maps to NM_152395.2 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr3:131100936 G>A maps to NM_152395.2 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr16:4743762 C>T maps to NM_032349.3 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr16:4745074 C>G maps to NM_032349.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr16:4745140 G>A maps to NM_032349.3 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:145586853 G>A maps to NM_001012758.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:145586821 C>T maps to NM_001012758.2 W289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr1:145587763 G>A maps to NM_001012758.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:33202725 G>T maps to NM_001105570.1 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:33183333 C>G maps to NM_001105570.1 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:63997455 G>A maps to NM_032344.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr11:63994360 C>A maps to NM_032344.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr11:63996988 G>C maps to NM_032344.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr11:63996765 C>T maps to NM_032344.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr10:12219888 G>A maps to ENST00000378937 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr10:12209769 G>C maps to ENST00000378937 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr10:12215812 C>T did not map to a codon.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr4:123843691 C>T maps to NM_007083.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr4:123843691 C>G maps to NM_007083.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr16:77775788 T>A maps to NM_001105663.1 L220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr16:77759450 C>G maps to NM_001105663.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr11:67397190 G>C maps to ENST00000376693 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr4:88344101 C>T maps to NM_024047.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr1:163317647 G>A maps to NM_145697.2 K348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:163306562 T>C maps to NM_145697.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr1:163306538 A>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:163315523 A>T maps to NM_145697.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr11:71726340 G>A maps to ENST00000393695 I742I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:71719866 G>A maps to ENST00000393695 R1701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:71728851 G>A maps to ENST00000393695 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:71725722 C>T maps to ENST00000393695 A948A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:71726868 C>G maps to ENST00000393695 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:71727177 G>A maps to ENST00000393695 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr11:71729551 C>T maps to ENST00000393695 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr11:71717194 G>A maps to ENST00000393695 L1866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr11:71727558 C>T maps to ENST00000393695 K385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr11:71727561 C>T maps to ENST00000393695 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr11:71729986 G>A maps to ENST00000393695 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:71729511 G>A maps to ENST00000393695 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr14:73743888 G>C maps to NM_001005743.1 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr19:41179339 C>T maps to NM_004756.3 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr19:41188698 T>C maps to NM_004756.3 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr19:41183209 G>A maps to NM_004756.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr12:69128496 G>T maps to NM_020401.2 E758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:69109477 C>G maps to NM_020401.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr12:69127365 G>T maps to NM_020401.2 E746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:229625721 G>A maps to NM_018230.2 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr1:229625747 G>C maps to NM_018230.2 S383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr1:229633912 A>G maps to NM_018230.2 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:229613467 G>C maps to NM_018230.2 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:229586336 C>A maps to NM_018230.2 E1039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:229635537 C>A maps to NM_018230.2 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr6:17669712 G>T maps to ENST00000430136 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr6:17616822 G>T maps to ENST00000430136 A1457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr6:17675189 G>A maps to ENST00000430136 Y266Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr6:17633030 G>A maps to ENST00000430136 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr6:17637525 A>C maps to ENST00000430136 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr5:37293027 T>C maps to NM_153485.1 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:37371052 C>T maps to NM_153485.1 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr5:37294508 G>A maps to NM_153485.1 F1284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr5:37331818 C>A maps to NM_153485.1 E533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr5:37350277 G>A maps to NM_153485.1 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:47858483 G>A maps to NM_015231.1 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr11:47833971 C>T maps to NM_015231.1 V654V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr11:47834456 C>T maps to NM_015231.1 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr11:47824992 C>T maps to NM_015231.1 Q924Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:47819814 C>A did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:47837036 C>T maps to NM_015231.1 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr11:47827864 C>T did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:131767775 C>T maps to NM_015354.1 F1568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr9:131745214 C>T maps to NM_015354.1 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr9:131767620 C>T maps to NM_015354.1 R1517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr9:131731763 C>T maps to NM_015354.1 Q295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr9:131765166 G>C maps to NM_015354.1 L1403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr9:131765609 G>A maps to NM_015354.1 V1437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:131765717 C>T maps to NM_015354.1 L1473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr9:131730867 A>G maps to NM_015354.1 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:131768006 C>T maps to NM_015354.1 F1607F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr9:131731693 C>T maps to NM_015354.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr7:135303234 C>T maps to NM_015135.2 L1283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr7:135255985 C>T maps to NM_015135.2 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr7:135269721 C>T maps to NM_015135.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:135261758 G>C maps to NM_015135.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:135263631 G>A maps to NM_015135.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:135329648 C>T maps to NM_015135.2 Q1856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:135272358 C>T maps to NM_015135.2 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:135333282 C>T maps to NM_015135.2 L2006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr7:135298915 C>T maps to NM_015135.2 Q1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr7:135291637 C>G maps to NM_015135.2 V1015V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr7:135320369 C>T maps to NM_015135.2 L1701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr7:135262737 C>T maps to NM_015135.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr7:135330312 G>A maps to NM_015135.2 S1927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr7:135310051 C>A maps to NM_015135.2 L1540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr7:135330312 G>A maps to NM_015135.2 S1927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:13393438 G>C maps to NM_024923.2 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:13401904 G>A maps to NM_024923.2 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr3:13363765 C>T maps to NM_024923.2 Q1614Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:13383322 G>A maps to NM_024923.2 I1051I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr3:13378403 G>A maps to NM_024923.2 V1189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:13376974 G>A maps to NM_024923.2 L1274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:13377103 G>A maps to NM_024923.2 I1231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr3:13376965 C>T maps to NM_024923.2 E1277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr3:13377028 C>T maps to NM_024923.2 V1256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr3:13381431 G>A maps to NM_024923.2 L1131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr3:13393426 G>C maps to NM_024923.2 T929T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr3:13415229 G>A maps to NM_024923.2 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr3:13415344 C>T maps to NM_024923.2 W487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:154018562 T>G maps to NM_207308.2 L1226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:154000003 G>A maps to NM_207308.2 Q1309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:154042812 G>A maps to NM_207308.2 F830F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:154072515 G>T maps to NM_207308.2 Y641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr1:153967639 G>A maps to NM_207308.2 S1801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr1:154115946 C>G maps to NM_207308.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:153998044 G>A maps to NM_207308.2 V1365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr1:154076506 G>C maps to NM_207308.2 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr1:154090257 C>T maps to NM_207308.2 G521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr9:134026094 G>A maps to ENST00000451030 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr9:134020057 G>A maps to ENST00000451030 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr9:134034769 G>T maps to ENST00000451030 E814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr9:134021688 C>A maps to ENST00000451030 S648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr9:134034795 G>A maps to ENST00000451030 V822V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr9:134034816 G>C maps to ENST00000451030 V829V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr6:150057649 T>C maps to NM_198887.1 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr6:150048188 C>T maps to NM_198887.1 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr4:77055452 G>A maps to ENST00000458189 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr4:77045828 G>C maps to ENST00000458189 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:106418346 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:73205990 C>T maps to NM_024844.3 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr17:73231252 C>G maps to NM_024844.3 S609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr17:73231772 G>A maps to NM_024844.3 *657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:73229200 C>A maps to NM_024844.3 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr17:73221212 C>T maps to NM_024844.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr17:5317410 G>A maps to NM_002532.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:56857668 G>A maps to NM_014669.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr16:56782201 C>T maps to NM_014669.3 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr16:56782201 C>T maps to NM_014669.3 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr16:56782201 C>T maps to NM_014669.3 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr16:56871557 G>C maps to NM_014669.3 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr11:3716746 G>A maps to NM_016320.4 Q1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:3707309 G>C maps to NM_016320.4 L1523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr11:3789861 G>T maps to NM_016320.4 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr11:3716786 T>A maps to NM_016320.4 S1353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr11:3720357 G>C maps to NM_016320.4 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr11:3704661 C>T maps to NM_016320.4 E1562E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr11:3742044 G>A maps to NM_016320.4 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr11:3721909 C>T maps to NM_016320.4 L1224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr11:3800410 G>C maps to NM_016320.4 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr13:25876000 C>T maps to NM_014089.3 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr13:25914232 G>A maps to NM_014089.3 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr13:25901110 G>A maps to NM_014089.3 Q363Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:23240295 C>T maps to ENST00000413919 Q427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr7:23240087 G>C maps to ENST00000413919 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:23224755 C>T maps to ENST00000413919 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr15:41657736 G>C maps to NM_016359.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr16:67904708 G>T maps to NM_005796.1 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:224477269 C>T maps to NM_002533.2 Q497Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr1:224495739 G>A maps to NM_002533.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr1:224475611 C>G maps to NM_002533.2 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr19:16918748 C>G maps to ENST00000438489 V1363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:16910735 C>T maps to ENST00000438489 L1167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:16860124 C>T maps to ENST00000438489 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr19:16860862 G>A maps to ENST00000438489 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr19:16902159 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr19:16860124 C>G maps to ENST00000438489 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:62570908 C>T maps to NM_006362.4 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:62563951 G>A maps to NM_006362.4 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:101581399 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr23:102334725 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr23:102337229 G>C did not map to a codon.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr23:102338590 C>A did not map to a codon.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr23:102337194 G>C did not map to a codon.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr23:102334548 G>C did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:102339337 T>A did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr23:102337947 T>A did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:102334739 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr23:102332664 G>A did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr23:101096055 C>A did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:101096683 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr23:101095526 T>C did not map to a codon.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr17:706927 G>A maps to NM_022463.3 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr19:17571579 C>A maps to NM_138454.1 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr9:91150577 C>T maps to NM_001161625.1 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr9:91150560 C>G maps to NM_001161625.1 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr7:8790657 G>A maps to NM_152745.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr12:57619091 C>T maps to NM_007224.3 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr14:24885812 G>T maps to NM_025081.2 E1620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr14:24885463 C>A maps to NM_025081.2 G1503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:24880395 G>A maps to NM_025081.2 K843K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr14:24885205 C>T maps to NM_025081.2 L1417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr14:24885496 C>T maps to NM_025081.2 L1514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr14:24884980 C>T maps to NM_025081.2 S1342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr14:24885118 C>T maps to NM_025081.2 L1388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr14:24880407 G>A maps to NM_025081.2 V847V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr14:24878128 C>T maps to NM_025081.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr14:24886354 C>A maps to NM_025081.2 L1800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr14:24877355 C>A maps to NM_025081.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr14:24884779 C>T maps to NM_025081.2 L1275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr14:24884815 C>T maps to NM_025081.2 P1287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr23:41333582 G>A did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:41333265 C>T did not map to a codon.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr23:41333527 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr23:41333008 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:113348979 G>A maps to NM_001032409.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr12:113355507 G>C maps to NM_002534.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr12:113435516 G>T maps to NM_016817.2 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr12:113448261 G>T maps to NM_016817.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:113416526 G>A maps to NM_016817.2 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:113416551 G>T maps to NM_016817.2 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr12:113433188 C>T maps to NM_016817.2 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:113416526 G>A maps to NM_016817.2 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr12:113400618 C>T maps to NM_006187.2 Q666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr12:113385858 C>T maps to NM_006187.2 C328C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr12:113405325 A>G maps to NM_006187.2 Q931Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr12:121476720 G>A maps to NM_003733.2 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr12:121458861 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr12:121476642 C>G maps to NM_003733.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr15:64983648 G>C maps to ENST00000403937 S52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:151740601 C>T maps to ENST00000321531 H123H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:151743616 C>T maps to ENST00000321531 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr10:105657329 C>T maps to NM_024928.4 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:56618690 G>T maps to NM_024068.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:138439762 C>T maps to NM_014582.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr9:138438706 G>A maps to NM_014582.2 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr9:136081313 G>T maps to NM_014581.2 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr1:228558964 C>A maps to NM_001098623.1 S6829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:228433260 C>G maps to NM_001098623.1 S1210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:228527733 G>T maps to NM_001098623.1 E5783*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BL-A3JM-01A-12D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:228400371 C>G maps to ENST00000337335 *159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:228471294 G>A maps to NM_001098623.1 A2943A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr1:228462330 C>T maps to NM_001098623.1 G1914G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr1:228547933 C>T maps to NM_052843.2 H6447H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:228466438 G>A maps to NM_001098623.1 E2303E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr1:228473992 G>A maps to NM_001098623.1 S3073S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr1:228558953 C>T maps to NM_001098623.1 F6825F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:228523513 G>A maps to NM_001098623.1 E5476E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr1:228556047 C>T maps to NM_001098623.1 V6566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr1:228401893 C>G maps to NM_001098623.1 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:228464925 C>T maps to NM_001098623.1 L2222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr1:228473944 C>T maps to NM_001098623.1 P3057P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:228399582 C>T maps to NM_001098623.1 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr1:228433249 G>A maps to NM_001098623.1 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:228403279 G>A maps to NM_001098623.1 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr1:228494154 T>A maps to NM_001098623.1 S3914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:228528869 C>T maps to NM_001098623.1 L5924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr1:228548179 C>G maps to NM_052843.2 L6529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr1:228504575 C>T maps to NM_001098623.1 A4484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr1:228400284 C>T maps to NM_001098623.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:228412241 C>T maps to NM_001098623.1 C912C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr2:220429982 G>A maps to NM_015311.2 F796F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:220434967 G>A maps to NM_015311.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr2:220430009 C>T maps to NM_015311.2 E787E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr2:220435264 G>T maps to NM_015311.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:220435210 G>A maps to NM_015311.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr8:133041347 C>T maps to ENST00000262283 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr8:133047064 C>T maps to ENST00000262283 Q444Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr15:28267710 G>A maps to NM_000275.2 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr15:28326942 G>A maps to NM_000275.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr15:28090151 C>G maps to NM_000275.2 G795G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr15:28211932 G>A maps to NM_000275.2 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr15:28000566 G>C maps to NM_000275.2 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr15:28234812 C>G did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr15:28231759 C>T maps to NM_000275.2 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr15:28211893 G>A maps to NM_000275.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr15:28277233 C>T maps to NM_000275.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:17339097 G>T maps to NM_024578.1 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr19:17339730 C>T maps to NM_024578.1 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr4:48852064 C>T maps to NM_001168254.1 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr4:48901919 G>C maps to NM_001014446.1 S30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr4:48896039 G>T maps to NM_001014446.1 S83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr5:68805246 C>A maps to NM_002538.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr7:97619395 G>A maps to NM_006188.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr23:128696761 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr23:128694595 T>C did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:128723852 A>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:128722902 C>A did not map to a codon.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr23:128721030 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:128710426 C>T did not map to a codon.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr4:71067185 C>T maps to NM_017855.3 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:10581666 C>A maps to NM_002539.1 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr2:10581773 C>A maps to NM_002539.1 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:103564038 C>T maps to NM_024410.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr9:131243908 G>A maps to NM_153435.1 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr9:131219716 G>T did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr9:131256910 C>T maps to NM_153435.1 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr9:131256925 C>T maps to NM_153435.1 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:86836724 C>T maps to ENST00000370567 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr22:50969698 C>G maps to NM_001014440.3 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr15:76019754 A>G maps to NM_175881.3 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr15:76017545 G>A maps to NM_175881.3 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr23:123514841 G>A did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr23:123538963 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr23:123780660 C>T did not map to a codon.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:123654562 C>G did not map to a codon.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:123657462 C>A did not map to a codon.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr23:123805550 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr23:123556133 C>G did not map to a codon.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr23:123519799 G>A did not map to a codon.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr23:123870928 C>A did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr23:123516589 A>G did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr23:124097479 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:123516581 A>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:123554353 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:123785873 G>A did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr23:123785803 T>C did not map to a codon.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr23:123526110 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr23:123779048 C>A did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr23:123657407 C>G did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:123518336 T>A did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:123680940 C>G did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:123657221 C>G did not map to a codon.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr23:123517666 C>G did not map to a codon.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr23:123637418 G>A did not map to a codon.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr23:123554331 G>A did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:123514391 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:123518385 A>G did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:123779156 C>G did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:123697600 C>T did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr23:123657343 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:123517710 T>C did not map to a codon.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr23:123519766 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:123637413 T>A did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr23:123525954 T>G did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr23:123525967 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr23:123780575 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr23:123538943 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:123680845 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr23:123871034 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr23:123526164 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr5:167551960 G>A maps to NM_001122679.1 Q705Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:167655044 G>A maps to NM_001122679.1 L1801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:167553930 A>G maps to NM_001122679.1 E794E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr5:167674420 G>A maps to NM_001122679.1 R2150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:183664473 G>A maps to NM_001080477.1 A1177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr4:183675803 G>C maps to NM_001080477.1 R1428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr4:183696287 C>T maps to NM_001080477.1 V1762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:183694774 C>T maps to NM_001080477.1 I1681I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr4:183245280 C>A maps to NM_001080477.1 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr4:183603144 G>A maps to NM_001080477.1 W671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr4:183603147 T>A maps to NM_001080477.1 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr4:183603108 T>A maps to NM_001080477.1 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr4:183609316 A>G did not map to a codon.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:183710448 C>T maps to NM_001080477.1 T1836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr4:183522098 C>G maps to NM_001080477.1 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr4:183603123 C>T maps to NM_001080477.1 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr4:183676061 G>A maps to NM_001080477.1 A1514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr4:183245370 G>A maps to NM_001080477.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr4:183713923 G>C maps to NM_001080477.1 V2033V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr11:78433750 G>T maps to NM_001098816.2 I1254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:78516496 G>A maps to NM_001098816.2 C673C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:78413034 G>T maps to NM_001098816.2 S1541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr11:78380888 G>A maps to NM_001098816.2 T2167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr23:13757018 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:13765052 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:13773332 A>C did not map to a codon.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr23:13779315 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:13776465 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:13776488 C>G did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr23:13780469 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:13754677 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:13754643 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:13764499 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:13753385 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr23:13764960 A>T did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr7:44739834 A>G maps to ENST00000444676 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr7:44739759 C>T maps to ENST00000444676 F832F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr7:44737335 G>C maps to ENST00000444676 R786R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr7:44664044 C>T maps to ENST00000444676 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr7:44736642 C>T maps to ENST00000444676 D692D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr7:44734096 C>T maps to ENST00000444676 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr7:44664044 C>T maps to ENST00000444676 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr10:50966536 G>A maps to NM_018245.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr10:50958925 G>A maps to NM_018245.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr10:50947853 G>T maps to NM_018245.2 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr10:50959988 G>A maps to NM_018245.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr10:50945874 C>T maps to NM_018245.2 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr12:123463886 C>T maps to ENST00000228922 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr20:61441892 G>A maps to NM_007346.2 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr20:61444808 A>G maps to NM_007346.2 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr20:61444835 C>A maps to NM_007346.2 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr6:72006209 G>C maps to NM_024576.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr3:9796492 G>A maps to NM_016821.2 W224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:95155526 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr23:70784472 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr23:70784469 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr23:70775116 A>G did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:70784452 C>A did not map to a codon.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr23:70777104 G>C did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:70787372 T>C did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:70764431 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr15:41624730 G>C maps to NM_007280.1 S10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr10:74690367 C>T maps to NM_152635.1 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr2:174946671 C>T maps to ENST00000409546 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:138011384 C>T maps to NM_014279.4 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr9:137987733 G>T maps to NM_014279.4 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr9:138011648 G>A maps to NM_014279.4 E343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:9967497 G>A maps to NM_058164.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr19:9965401 G>A maps to NM_058164.2 N275N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr19:9964870 C>A maps to NM_058164.2 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr1:102269865 G>C maps to ENST00000338858 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr1:102270270 C>A maps to ENST00000338858 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr13:53602985 C>T maps to NM_006418.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr11:7530938 G>A maps to NM_198474.3 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:7531262 C>T maps to NM_198474.3 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr11:7531132 G>A maps to NM_198474.3 W308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr9:127561622 C>T maps to NM_182487.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:161954645 A>G maps to ENST00000451379 Y534Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:161993193 G>A maps to ENST00000451379 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:161953864 G>C maps to ENST00000451379 S619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:114524372 G>A maps to NM_020190.2 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr6:137814905 G>A maps to NM_175747.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr6:137814776 G>A maps to NM_175747.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:10324643 C>T maps to NM_002543.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr17:29622896 G>C maps to NM_002544.4 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:53081807 C>A maps to NM_004498.1 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr18:55103601 C>A maps to NM_004852.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr18:55143771 C>T maps to NM_004852.2 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:74079007 G>A maps to NM_001080507.2 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr6:74078931 G>A maps to NM_001080507.2 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr3:193332656 C>T maps to NM_130837.2 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr3:193361160 G>C did not map to a codon.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr3:193353260 A>T maps to NM_130837.2 K300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr3:193335030 G>A maps to NM_130837.2 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr3:193332697 G>A maps to NM_130837.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr10:98111143 C>T maps to NM_033207.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr11:132306604 C>A maps to NM_002545.3 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr11:132527207 G>T maps to NM_002545.3 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr11:132399054 G>A maps to NM_002545.3 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr11:132399052 G>C maps to NM_002545.3 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:67454410 T>A did not map to a codon.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr23:67268294 G>A did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr23:67283763 C>A did not map to a codon.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr23:67283837 C>A did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr23:67431997 T>C did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:67652754 G>C did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:67413750 G>T did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:67273547 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:67430090 T>C did not map to a codon.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr23:67431952 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr23:67518913 A>C did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr8:145111639 C>T maps to ENST00000360660 E575E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr8:145112920 G>A maps to ENST00000360660 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr8:145113542 G>A maps to ENST00000360660 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr8:145106227 C>G maps to ENST00000360660 *1288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr8:145111912 G>A maps to ENST00000360660 D548D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr8:145109729 C>G maps to ENST00000360660 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr23:153420213 G>A did not map to a codon.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr23:153416240 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:153418476 C>A did not map to a codon.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr23:153420203 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr23:153421924 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr23:153421954 G>A did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:153496063 G>A did not map to a codon.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr23:153459032 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr7:128414713 G>A maps to NM_001708.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:241803277 G>A maps to NM_014322.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr1:241767756 C>T maps to NM_014322.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr1:241767765 G>C maps to NM_014322.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr1:241761104 G>C maps to NM_014322.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:241803418 C>T maps to NM_014322.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr10:88414587 G>A maps to NM_001030015.2 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr6:47754314 G>A maps to ENST00000489301 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr6:47763028 C>T maps to ENST00000489301 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr1:29189572 G>T maps to NM_000911.3 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr8:54147421 G>A maps to NM_000912.3 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr8:54142078 A>G maps to NM_000912.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr20:62724216 C>T maps to NM_000913.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr20:62724216 C>T maps to NM_000913.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr20:62730139 G>A maps to NM_000913.3 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr20:62729980 C>G maps to NM_000913.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr6:154412525 G>A maps to NM_001145279.1 E454E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:203467965 G>C maps to NM_014359.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr1:203466221 C>T maps to NM_014359.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:203465268 C>T maps to NM_014359.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:13160938 C>T maps to NM_021980.4 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr10:13161004 G>A maps to NM_021980.4 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr10:13164453 G>A maps to NM_021980.4 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:13154580 C>G maps to NM_021980.4 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr10:13167527 C>G maps to NM_021980.4 S370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr11:6891293 T>A maps to NM_001004460.1 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr11:6891395 C>T maps to NM_001004460.1 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr11:6891509 C>T maps to NM_001004460.1 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr11:7960812 G>C maps to NM_001003745.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:6897885 G>A maps to NM_207186.2 W3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr11:6866954 C>T maps to ENST00000379831 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr11:7950074 A>G maps to NM_001004461.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr12:55615693 G>T maps to NM_001005280.1 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:48596817 G>C maps to NM_001004134.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:48596610 G>T maps to NM_001004134.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:55735849 C>T maps to NM_001005491.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr11:55735792 G>A maps to NM_001005491.1 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr11:55735288 C>T maps to NM_001005491.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr6:29408454 C>A maps to NM_013941.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr6:29408406 C>A maps to NM_013941.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr14:22102305 C>T maps to NM_001005466.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:123886664 G>A maps to NM_001004462.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr11:123909048 G>A maps to NM_001004463.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:123900607 C>T maps to NM_001004464.1 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:123900526 C>T maps to NM_001004464.1 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr11:123900583 C>T maps to NM_001004464.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:123893844 C>A maps to NM_001001953.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr11:123894477 C>A maps to NM_001001953.1 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:15918787 G>A maps to NM_013940.2 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr19:15918826 G>A maps to NM_013940.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr19:15918297 G>A maps to NM_013940.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr19:15839116 C>G maps to NM_013939.2 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr19:15839446 G>A maps to NM_013939.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr19:15839674 G>T maps to NM_013939.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr19:15905703 C>T maps to NM_001004466.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:159409592 G>A maps to NM_012351.2 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr1:159409970 G>T maps to NM_012351.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr1:159410478 C>T maps to NM_012351.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr1:159410054 G>A maps to NM_012351.2 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:159284101 G>A maps to NM_001004467.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr1:159284302 A>T maps to NM_001004467.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr1:158436235 G>A maps to NM_001004473.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:158436070 C>A maps to NM_001004473.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:158436061 C>A maps to NM_001004473.1 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr1:158390584 C>T maps to NM_001004476.1 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:158390575 G>C maps to NM_001004476.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:158389927 A>G maps to NM_001004476.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr12:56030899 T>C maps to NM_206899.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:56031595 G>A maps to NM_206899.1 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr12:56030770 T>C maps to NM_206899.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr11:57996149 G>A maps to NM_001004471.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:158450114 C>T maps to NM_001004472.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr1:158449926 C>G maps to NM_001004472.1 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:158450383 C>T maps to NM_001004472.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr11:123848194 G>C maps to NM_001004474.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr11:123847717 G>A maps to NM_001004474.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr11:123848239 A>C maps to NM_001004474.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr11:123848194 G>A maps to NM_001004474.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:158368902 C>T maps to NM_001004475.1 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:59480924 G>A maps to NM_001005324.1 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr1:158548960 C>T maps to NM_001004477.1 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:158548927 G>A maps to NM_001004477.1 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:158576654 C>T maps to NM_001004478.1 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:158576911 C>T maps to NM_001004478.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:158576308 C>G maps to NM_001004478.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr6:29395175 T>C maps to NM_013937.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr6:29394815 G>A maps to NM_013937.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr14:20666303 T>A maps to NM_001005503.1 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:19378097 C>T maps to NM_001013354.1 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr14:19377742 T>C maps to NM_001013354.1 Y50Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:248004358 C>A maps to NM_001001959.1 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr1:248005057 G>A maps to NM_001001959.1 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr6:29364884 C>T maps to NM_013936.3 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:29342572 C>G maps to NM_030959.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr6:29342815 G>T maps to ENST00000396806 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:107367386 G>A maps to NM_001004481.1 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr9:107367089 C>T maps to NM_001004481.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr9:107298744 G>C maps to NM_001001961.1 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr9:107298071 C>G maps to NM_001001961.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:107289385 G>A maps to NM_001001919.1 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr9:107288605 G>A maps to NM_001001919.1 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr9:107267010 C>G maps to NM_001004485.1 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:247835818 G>A maps to NM_001005487.1 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:130678547 C>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:130678917 C>A did not map to a codon.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr23:130678904 C>T did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr23:130678773 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:130678453 T>A did not map to a codon.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr23:130678905 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr23:130678902 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:35869591 G>T maps to NM_001004487.1 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr9:35869948 G>A maps to NM_001004487.1 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr9:35869567 G>C maps to NM_001004487.1 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr1:247978920 C>T maps to NM_001001966.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr1:248512570 C>T maps to NM_001001918.1 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:248512531 C>A maps to NM_001001918.1 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:248512831 A>T maps to NM_001001918.1 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:248512711 C>T maps to NM_001001918.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr1:248845224 G>T maps to NM_001004734.1 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:248845593 G>C maps to NM_001004734.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr6:29274778 C>T maps to NM_030946.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr6:29275347 C>T maps to NM_030946.1 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr6:29274591 C>G maps to NM_030946.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr17:3119783 G>A maps to NM_014565.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr17:3119720 C>T maps to NM_014565.2 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr17:3100985 C>T maps to NM_012352.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr17:3101036 C>T maps to NM_012352.1 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr9:125391655 C>T maps to NM_001004450.1 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:247920937 G>A maps to NM_012353.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr17:3300969 C>G maps to NM_003553.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:3254992 C>T maps to NM_012360.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:3030221 G>T maps to ENST00000381953 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:15198235 C>T maps to NM_001004713.1 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr9:125273429 C>G maps to ENST00000444856 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr9:125273325 G>A maps to ENST00000444856 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr9:125562418 G>A maps to NM_080859.1 E6E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr9:125424128 C>T maps to ENST00000373686 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr9:125486351 C>G maps to NM_001005235.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:125487146 G>C maps to NM_001005235.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:125486867 G>A maps to NM_001005235.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr9:125486318 C>A maps to NM_001005235.1 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr9:125512170 C>G maps to ENST00000373684 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:125512725 G>A maps to ENST00000373684 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr9:125330240 G>T maps to NM_001004454.1 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:9204519 C>G maps to ENST00000305465 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr19:9204000 C>G maps to ENST00000305465 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr19:9204615 C>T maps to ENST00000305465 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr9:125316095 C>A maps to NM_001004457.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:125377336 C>T maps to NM_012364.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr11:57982755 C>G maps to NM_001004458.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:57982647 T>C maps to NM_001004458.1 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr11:57982323 T>C maps to NM_001004458.1 H36H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr11:57982692 C>T maps to NM_001004458.1 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr11:57982878 C>T maps to NM_001004458.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr7:143793099 A>G maps to NM_001004135.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:143792826 G>A maps to NM_001004135.1 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr7:143792886 T>C maps to NM_001004135.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr7:143826870 C>T maps to NM_001001659.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr7:143826315 C>A maps to NM_001001659.1 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr7:143807076 C>T maps to NM_001005480.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr7:143806803 C>A maps to NM_001005480.2 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:143772157 C>A maps to NM_001004488.1 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:143747956 C>T maps to NM_012365.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr7:99473756 C>G maps to NM_001005276.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr11:6807164 G>A maps to NM_001004489.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:6789912 G>T maps to NM_001004490.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:248129259 G>A maps to NM_001004491.1 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr1:247614708 C>T maps to NM_001004492.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr6:27879040 G>A maps to NM_033057.2 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr6:27879692 G>A maps to NM_033057.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr16:3406137 C>G maps to NM_012368.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr1:247695366 G>A maps to NM_198074.4 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr1:247694934 C>T maps to NM_198074.4 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr11:6942834 G>A maps to NM_001004684.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:143657917 G>A maps to NM_012369.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr7:143657848 C>G maps to NM_012369.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr7:143632513 C>A maps to NM_001004685.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:143632801 G>A maps to NM_001004685.1 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr7:143632954 T>C maps to NM_001004685.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr7:143632726 C>A maps to NM_001004685.1 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr1:247752613 G>C maps to NM_001001915.1 *318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:247752305 A>T maps to NM_001001915.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr1:247752389 C>G maps to NM_001001915.1 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr1:247768985 C>T maps to NM_001001914.1 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:248685405 C>T maps to NM_001013355.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:248685807 C>T maps to NM_001013355.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:248685288 C>T maps to NM_001013355.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr6:29430085 A>G maps to NM_030883.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr6:29429620 C>T maps to NM_030883.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:29556416 G>A maps to NM_007160.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:29141852 G>A maps to NM_030905.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr6:29141693 G>A maps to NM_030905.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr6:29142222 C>T maps to NM_030905.2 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr6:29141531 G>A maps to NM_030905.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:29142011 C>G maps to NM_030905.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:29080098 C>T maps to NM_001005216.2 C144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr1:248262934 C>T maps to NM_175911.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:248263102 G>A maps to NM_175911.2 K142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:248202321 T>A maps to NM_001004686.2 Y251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:248224483 T>C maps to NM_001004687.1 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr1:248224920 A>G maps to NM_001004687.1 *313W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr1:248224041 C>G maps to NM_001004687.1 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:248112659 T>C maps to NM_001001963.1 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr1:248343674 C>T maps to NM_001004688.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:248344189 C>T maps to NM_001004688.1 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr1:248366920 A>G maps to NM_001004689.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr1:248366467 C>A maps to NM_001004689.1 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr1:248367202 C>T maps to NM_001004689.1 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr1:248402796 C>A maps to NM_017504.1 C189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr1:248309249 C>T maps to NM_001004690.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr1:248308667 C>T maps to NM_001004690.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr1:248487243 G>A maps to NM_001004691.1 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:248487039 G>A maps to NM_001004691.1 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr1:248570297 C>T maps to NM_030904.1 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr1:248569429 C>A maps to NM_030904.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr1:248756565 G>A maps to NM_001004693.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr1:248756793 G>A maps to NM_001004693.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr1:248756643 G>C maps to NM_001004693.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:248756425 G>T maps to NM_001004693.1 S215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:248789574 G>A maps to NM_001001964.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr1:248458280 G>A maps to NM_001004692.1 C200C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:248616328 C>T maps to NM_001004136.1 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:248616409 C>G maps to NM_001004136.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr1:248637271 C>T maps to NM_001005495.1 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr1:248637605 T>A maps to NM_001005495.1 *319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:248436918 G>A maps to NM_001004695.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr1:248436540 G>A maps to NM_001004695.1 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:248436696 C>G maps to NM_001004695.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr1:248436750 C>T maps to NM_001004695.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr1:248737332 G>C maps to NM_001001821.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:248737371 G>A maps to NM_001001821.1 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr1:248525925 G>A maps to NM_001004696.1 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr1:248525346 C>T maps to NM_001004696.1 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr1:248525632 T>C maps to NM_001004696.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr1:248651987 G>A maps to NM_001004697.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:248551674 T>C maps to NM_001005471.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:248551673 C>A maps to NM_001005471.1 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:248551799 G>C maps to NM_001005471.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr1:248084408 G>T maps to NM_001005522.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:248084414 C>T maps to NM_001005522.1 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr1:248084687 T>G maps to NM_001005522.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr1:248084483 G>A maps to NM_001005522.1 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr1:248084459 T>C maps to NM_001005522.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr5:180582133 C>T maps to NM_206880.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr6:29012934 A>G maps to NM_030903.3 Y6Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr1:248059028 G>A maps to NM_001001957.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:248059564 T>G maps to NM_001001957.2 L226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:248059763 C>A maps to NM_001001957.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr1:247654468 C>T maps to NM_001004698.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr5:180166809 G>A maps to NM_001001657.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:8841488 C>T maps to NM_001004699.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:8842007 C>T maps to NM_001004699.1 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:3195372 C>T maps to ENST00000397187 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr17:3194929 C>G maps to ENST00000397187 *322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr17:3195489 G>A maps to ENST00000397187 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:3181431 G>A maps to NM_002551.3 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr17:3181778 T>G maps to NM_002551.3 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr17:3324613 C>G maps to NM_012373.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:3324751 T>G maps to NM_012373.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr11:55135820 C>T maps to NM_001005275.1 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr11:55135607 G>A maps to NM_001005275.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:48511050 C>G maps to NM_001005512.2 S236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:48510812 C>T maps to NM_001005512.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr11:51412329 T>C maps to NM_001005272.3 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:48239179 C>A maps to NM_001005470.1 Y273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr11:48238597 C>T maps to NM_001005470.1 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr11:55371621 G>T maps to NM_001004700.1 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr11:55371372 G>A maps to NM_001004700.1 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr11:55371009 G>C maps to NM_001004700.1 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr11:55370988 C>T maps to NM_001004700.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr11:49974405 A>G maps to NM_001001955.2 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr11:55322408 C>T maps to NM_001001920.1 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr11:55322291 C>T maps to NM_001001920.1 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr11:55322490 T>C maps to NM_001001920.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr11:55322564 C>T maps to NM_001001920.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:55339743 C>G maps to NM_001004701.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr11:48346953 C>G maps to NM_001004702.1 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr11:48347199 C>T maps to NM_001004702.1 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr11:51515493 T>C maps to NM_001004703.1 Y71Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr11:51515721 G>A maps to NM_001004703.1 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr11:51515472 C>T maps to NM_001004703.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr11:55433538 C>T maps to NM_001004704.1 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:55433226 C>T maps to NM_001004704.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr11:55433505 G>A maps to NM_001004704.1 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr11:55433034 G>A maps to NM_001004704.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr11:55433082 G>A maps to NM_001004704.1 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:56233156 C>T maps to NM_012374.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:56233149 C>T maps to NM_012374.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr17:56232573 C>G maps to NM_012374.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr11:59245828 T>C maps to NM_001004705.1 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr11:59245788 C>G maps to NM_001004705.1 S296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr11:59245435 C>T maps to NM_001004705.1 Y178Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:59271962 C>T maps to NM_001004706.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr11:59271356 C>T maps to NM_001004706.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr11:59271311 G>A maps to NM_001004706.1 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr17:56247357 C>T maps to NM_001004707.3 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr17:56247786 C>G maps to NM_001004707.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:123811072 C>T maps to NM_001001965.1 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr11:123810815 C>T maps to NM_001001965.1 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:59224918 G>A maps to NM_001004708.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr11:59224852 G>C maps to NM_001004708.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr11:59224444 C>A maps to NM_001004708.1 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr11:59282717 C>T maps to NM_001004711.1 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:59283251 G>T maps to NM_001004711.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:59283287 G>A maps to NM_001004711.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr11:59282630 G>C maps to NM_001004711.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr11:59283290 G>A maps to NM_001004711.1 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr14:22133601 C>T maps to NM_001001912.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr14:22134222 G>A maps to NM_001001912.1 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr14:22133301 C>T maps to NM_001001912.1 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:102358493 C>T maps to NM_001001674.1 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr15:102462383 C>T maps to NM_001004195.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr15:102345981 G>A maps to NM_001005326.1 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:20404493 C>T maps to NM_001004063.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr14:20404691 G>C maps to NM_001004063.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr14:20404637 T>G maps to NM_001004063.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr14:20502476 G>A maps to NM_001004714.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr14:20502371 G>A maps to NM_001004714.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr14:20482424 G>A maps to NM_001004712.1 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:20444468 G>A maps to NM_001005486.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr14:20444033 T>C maps to NM_001005486.1 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr14:20585727 G>T maps to NM_001004715.1 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr14:20586059 C>T maps to NM_001004715.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr14:20586512 T>C maps to NM_001004715.1 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr14:20345190 C>T maps to NM_001005501.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr14:20389115 G>A maps to NM_001005483.1 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr14:20528871 C>G maps to NM_001004717.1 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr14:20528871 C>A maps to NM_001004717.1 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr14:20249269 A>G maps to NM_001005500.1 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr14:20248954 A>T maps to NM_001005500.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr14:20249176 T>A maps to NM_001005500.1 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr14:20249080 C>T maps to NM_001005500.1 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr15:22368919 C>T maps to NM_001004719.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr15:22368670 A>T maps to NM_001004719.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr15:22369078 C>T maps to NM_001004719.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr15:22369238 C>T maps to NM_001004719.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr15:22369078 C>T maps to NM_001004719.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr14:20296467 T>A maps to NM_001004723.1 Y287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr14:20296167 G>C maps to NM_001004723.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr15:22382960 C>T maps to NM_001005241.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr15:22383191 C>T maps to NM_001005241.1 C240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr15:22383398 A>G maps to NM_001005241.1 Q309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr15:22383119 T>G maps to NM_001005241.1 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr15:22383257 C>T maps to NM_001005241.1 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr15:22383257 C>T maps to NM_001005241.1 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr14:20612220 G>T maps to NM_001004724.1 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr14:20612487 G>A maps to NM_001004724.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr11:55406009 C>T maps to NM_001004124.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:55406748 C>T maps to NM_001004124.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr14:20215774 T>C maps to NM_172194.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr14:20216305 C>A maps to NM_172194.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr14:20215690 C>A maps to NM_172194.1 Y35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr14:20216308 T>C maps to NM_172194.1 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr14:20215933 G>A maps to NM_172194.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:48328334 T>C maps to NM_001004725.1 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr11:48328196 G>C maps to NM_001004725.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr11:55419239 G>A maps to NM_001004059.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:55418471 C>T maps to NM_001004059.2 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:48285747 C>G maps to NM_001004726.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr11:48286146 C>T maps to NM_001004726.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr11:48285820 C>T maps to NM_001004726.1 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:48266717 G>A maps to NM_001004727.1 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:48267008 C>T maps to NM_001004727.1 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:48267149 G>A maps to NM_001004727.1 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr11:4976490 G>T maps to NM_001004748.1 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr11:4976304 A>G maps to NM_001004748.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr11:4976172 G>A maps to NM_001004748.1 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr11:4967691 A>G maps to NM_001005329.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr11:4968079 A>T maps to NM_001005329.1 L84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr11:4967559 G>A maps to NM_001005329.1 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr11:4967469 C>T maps to NM_001005329.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr11:4967424 C>T maps to NM_001005329.1 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:4928820 C>T maps to NM_001004749.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr11:4929159 G>A maps to NM_001004749.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr11:5344999 G>A maps to NM_033180.4 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr11:5322366 G>T maps to NM_033179.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr11:5322711 G>A maps to NM_033179.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr11:5363991 C>A maps to NM_001005567.1 G255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:5372784 A>C maps to NM_001004750.1 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:4661060 C>G maps to NM_001004751.2 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:4661040 G>A maps to NM_001004751.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:4661541 C>T maps to NM_001004751.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr11:4674622 C>T maps to NM_152430.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr11:4790640 A>G maps to ENST00000380383 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr11:4790463 G>A maps to ENST00000380383 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr11:4843355 G>A maps to NM_001004753.1 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr11:4843241 C>T maps to NM_001004753.1 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr11:4936548 G>A maps to NM_001005238.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr11:4936734 G>T maps to NM_001005238.1 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr11:5410828 G>A maps to NM_001004756.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr11:5410828 G>T maps to NM_001004756.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:5443928 C>T maps to NM_001004757.2 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:5444185 C>G maps to NM_001004757.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr11:5443477 C>A maps to NM_001004757.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr11:4869945 G>A maps to NM_001004758.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:5221177 G>A maps to NM_001004760.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr11:5221699 G>A maps to NM_001004760.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr11:5221420 G>T maps to NM_001004760.2 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr11:5172729 G>C maps to NM_012375.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr11:5172981 G>T maps to NM_012375.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:5142388 G>A maps to NM_001005222.2 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr11:5142809 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:5142583 A>T maps to NM_001005222.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr11:5153122 G>A maps to NM_001005160.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr11:6190836 G>A maps to NM_001004052.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:4388658 C>T maps to NM_001005161.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr11:4388618 C>A maps to NM_001005161.3 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr11:5510079 C>A maps to NM_001005163.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr11:5079880 C>T maps to NM_001005164.2 *326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:5080461 G>A maps to NM_001005164.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:5862956 G>A maps to ENST00000379946 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr11:5862664 A>G maps to ENST00000379946 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr11:5862419 G>C maps to ENST00000379946 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr11:5878253 G>A maps to NM_001005168.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr11:5878059 G>T maps to NM_001005168.1 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr11:5565994 G>C maps to NM_001005289.1 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr11:5566054 G>C maps to NM_001005289.1 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr11:4615933 T>C maps to ENST00000450052 Y247Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr11:4616014 G>A maps to ENST00000450052 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr11:4616238 C>G maps to ENST00000450052 S349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:4608386 C>T maps to NM_001005170.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr11:4608403 C>G maps to NM_001005170.2 S121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:4510813 C>A maps to NM_001005171.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr11:4471174 C>T maps to NM_001005172.2 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:4471444 A>C maps to NM_001005172.2 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:6007537 G>C maps to NM_001005173.2 S208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:4566579 G>T maps to NM_001004137.1 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr11:4566767 C>A maps to NM_001004137.1 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr11:5841756 C>T maps to NM_001005174.1 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr11:5841714 C>T maps to NM_001005174.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:5776113 C>G maps to NM_001005175.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr11:5799435 G>A maps to NM_001001922.2 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:4825151 C>G maps to ENST00000380382 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr11:6220473 C>G maps to NM_001005178.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr11:6220917 G>A maps to NM_001005178.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr11:6048688 G>A maps to NM_001001917.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:5968680 C>T maps to NM_001003443.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:5968854 C>T maps to NM_001003443.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr11:6023565 G>A maps to NM_001005179.2 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr11:6023418 C>T maps to NM_001005179.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:6023652 G>A maps to NM_001005179.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr11:5757851 C>T maps to NM_001005180.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr11:6129719 G>T maps to NM_001005181.1 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr11:6129403 C>T maps to NM_001005181.1 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr11:6129075 T>A maps to NM_001005181.1 L23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr11:59211156 C>T maps to NM_001004728.1 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr11:59211228 C>T maps to NM_001004728.1 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr11:59211278 C>A maps to NM_001004728.1 S213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr11:59210658 C>T maps to NM_001004728.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr11:59189679 C>T maps to NM_001001954.1 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:59190321 G>C maps to NM_001001954.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:59190144 G>T maps to NM_001001954.1 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr3:97806240 T>G maps to NM_054106.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:56757050 C>T maps to NM_001005323.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr11:56757008 G>A maps to NM_001005323.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:59132284 C>T maps to NM_001004729.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:59132260 G>C maps to NM_001004729.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr11:59132683 C>G maps to NM_001004729.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr11:56409282 A>G maps to NM_001002925.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr11:56409375 G>A maps to NM_001002925.1 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:55798343 C>T maps to NM_001001921.1 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:55798841 A>G maps to NM_001001921.1 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:55798059 C>T maps to NM_001001921.1 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr11:58126260 G>A maps to NM_001005489.1 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr11:58125940 G>C maps to NM_001005489.1 S201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:58189809 G>A maps to NM_001005566.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr11:58189909 G>A maps to NM_001005566.2 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr11:58190422 G>C maps to NM_001005566.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr11:58274927 G>A maps to NM_001005218.1 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:58170300 C>T maps to NM_001005469.1 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:58170579 G>A maps to NM_001005469.1 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr11:55541257 C>T maps to NM_001001967.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr11:55541542 G>A maps to NM_001001967.1 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr11:55563528 C>T maps to NM_001004735.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr11:55563246 T>C maps to NM_001004735.1 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:55563879 C>T maps to NM_001004735.1 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr11:55606418 C>T maps to NM_001005496.1 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr11:55587788 G>A maps to ENST00000395203 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr11:55587568 C>A maps to ENST00000395203 S157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr11:55587677 T>A maps to ENST00000395203 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr11:55587182 C>G maps to ENST00000395203 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr11:55587848 C>T maps to ENST00000395203 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr11:55761366 C>T maps to NM_003697.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:55761771 G>A maps to NM_003697.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr3:97851972 A>G maps to NM_001005338.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr3:97852308 C>G maps to NM_001005338.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr3:97868648 G>A maps to NM_001005514.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:97868372 C>T maps to NM_001005514.1 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr3:97868603 C>T maps to NM_001005514.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr3:97888416 C>T maps to NM_001005515.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:98002336 A>G maps to NM_001005482.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:98002423 A>G maps to NM_001005482.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr11:55703720 C>T maps to NM_006637.1 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr11:55703276 G>C maps to NM_006637.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr11:55944687 C>T maps to NM_001005492.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:98189001 C>T maps to NM_001004736.2 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr3:98189027 C>G maps to NM_001004736.2 S203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr3:98188846 C>T maps to NM_001004736.2 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:98217063 T>C maps to NM_001004737.1 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:98109712 G>C maps to NM_001005516.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr3:98110270 C>G maps to NM_001005516.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr3:98110248 C>G maps to NM_001005516.1 S247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:98072987 T>C maps to NM_001005517.1 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr11:55579376 T>C maps to NM_001004738.1 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr11:55579844 C>T maps to NM_001004738.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr11:55579130 C>T maps to NM_001004738.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr11:55579622 G>A maps to NM_001004738.1 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr11:55595170 C>T maps to NM_001004739.1 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr11:55594867 C>G maps to NM_001004739.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr11:55594882 C>T maps to NM_001004739.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr11:55595020 C>T maps to NM_001004739.1 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr11:55595182 T>C maps to NM_001004739.1 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr11:56380342 G>A maps to NM_001004740.1 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:56237064 G>A maps to NM_001004742.1 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:56237766 C>T maps to NM_001004742.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr11:56237918 G>A maps to NM_001004742.1 R19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr11:56237895 G>A maps to NM_001004742.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:56258183 G>A maps to NM_001005282.1 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr11:56258213 G>A maps to NM_001005282.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr11:56230094 G>T maps to NM_001004743.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr11:7818012 G>A maps to NM_153444.1 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr11:7817832 G>A maps to NM_153444.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:56185024 G>A maps to NM_001004744.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr11:56185063 G>T maps to NM_001004744.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:56043551 G>A maps to NM_001004745.1 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr11:56043950 T>G maps to NM_001004745.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr11:56020431 T>C maps to NM_001004747.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr11:56020565 T>G maps to NM_001004747.1 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr6:29323908 C>A maps to NM_030876.5 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr6:29323564 C>G maps to NM_030876.5 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr11:55681569 G>T maps to NM_001001960.1 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr11:55681983 C>A maps to NM_001001960.1 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr11:55681671 G>T maps to NM_001001960.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr11:55681566 G>A maps to NM_001001960.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr11:6816129 G>C maps to NM_003696.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FH-01A-11D-A38G-08 chr11:6816774 G>T maps to NM_003696.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr7:143701526 T>A maps to NM_001005281.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr7:143701886 C>T maps to NM_001005281.1 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr7:143701977 G>T maps to NM_001005281.1 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr7:143701409 C>G maps to NM_001005281.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:55714719 C>T maps to NM_001005182.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr12:55714856 C>G maps to NM_001005182.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr12:55715126 C>T maps to NM_001005182.1 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:55846107 A>G maps to NM_054105.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:55846761 C>T maps to NM_054105.1 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr12:55846881 G>A maps to NM_054105.1 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr12:55846128 C>T maps to NM_054105.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr12:55725552 G>A maps to NM_054104.1 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:55725669 C>T maps to NM_054104.1 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr12:55725742 A>T maps to NM_054104.1 K87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr12:55688665 G>A maps to NM_001005493.1 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr12:55688923 G>A maps to NM_001005493.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:55886709 G>A maps to NM_001005519.1 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr12:55886808 C>A maps to NM_001005519.1 Y221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr12:55863094 A>G maps to NM_001005499.1 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr12:55641106 T>G maps to NM_001005490.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:55820918 G>A maps to NM_001005183.1 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr12:55820540 C>T maps to NM_001005183.1 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr1:247875925 A>G maps to NM_001005286.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr1:247875921 A>G maps to NM_001005286.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr1:247875355 C>A maps to NM_001005286.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:158670234 C>A maps to NM_001005279.1 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:158670235 C>G maps to NM_001005279.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr1:158669953 A>G maps to NM_001005279.1 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr1:158669764 A>G maps to NM_001005279.1 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:158670124 G>T maps to NM_001005279.1 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:158687407 C>A maps to ENST00000368146 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr1:158687704 G>T maps to ENST00000368146 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr1:158687161 C>G maps to ENST00000368146 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:158725015 C>T maps to NM_001005184.1 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:158724898 G>A maps to NM_001005184.1 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:158725150 C>T maps to NM_001005184.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:158725015 C>T maps to NM_001005184.1 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:123676133 C>T maps to NM_001005325.1 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr11:123676457 A>T maps to NM_001005325.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:123676310 G>A maps to NM_001005325.1 H249H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:158736169 G>T maps to NM_001005185.1 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr1:158735917 C>T maps to NM_001005185.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr1:158735785 G>T maps to NM_001005185.1 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr1:158747278 G>A maps to NM_001005278.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:158746672 G>A maps to NM_001005278.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:158747167 G>A maps to NM_001005278.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:158747266 T>C maps to NM_001005278.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr11:57798885 G>A maps to NM_001005186.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr11:57799185 C>T maps to NM_001005186.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr11:57799167 C>T maps to NM_001005186.2 H248H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr14:21108980 T>C maps to NM_001001968.1 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr11:123813996 G>A maps to NM_001005187.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr7:142750261 G>A maps to NM_001001667.1 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr11:123624503 C>T maps to NM_001005188.1 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr1:158516977 G>A maps to NM_001005189.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr1:158517778 G>T maps to NM_001005189.1 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr1:158517010 G>T maps to NM_001005189.1 Y295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr19:14952605 A>G maps to NM_001005190.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:14952134 G>C maps to NM_001005190.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:14991432 G>C maps to NM_030901.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:14992002 G>C maps to NM_030901.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr19:14991481 G>C maps to NM_030901.1 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr19:14938183 A>G maps to NM_017506.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr19:14938807 C>T maps to NM_017506.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr19:14910902 C>A maps to NM_198944.1 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:14910579 G>A maps to NM_198944.1 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:14910474 G>C maps to NM_198944.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr19:9296801 G>C maps to NM_175883.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:9362192 C>T maps to NM_001079935.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr19:9213856 C>T maps to NM_001005193.1 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr19:9236987 C>T maps to NM_001001958.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr11:124440752 C>T maps to NM_001005194.1 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:124440002 C>T maps to NM_001005194.1 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:124412893 G>A maps to NM_001005195.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr11:124252741 G>C maps to NM_001005468.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr11:124252924 G>C maps to NM_001005468.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr11:124294446 G>C maps to NM_001005196.1 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:124294479 A>G maps to NM_001005196.1 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:124294197 G>A maps to NM_001005196.1 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:124310897 G>A maps to NM_012378.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr11:124310303 G>A maps to NM_012378.1 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:124310917 C>A maps to NM_012378.1 G22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr11:124179879 C>T maps to NM_001002917.1 K261K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr11:124189262 G>A maps to NM_001002918.1 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:124120461 C>T maps to ENST00000341493 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr11:56057738 A>T maps to NM_001005199.1 L267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:56058243 G>A maps to NM_001005199.1 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr11:55872741 C>G maps to NM_001005200.1 S75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr11:55872937 C>G maps to NM_001005200.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr11:55872895 C>T maps to NM_001005200.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr11:55873294 T>C maps to NM_001005200.1 Y259Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr11:55873138 G>A maps to NM_001005200.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:55890711 C>G maps to NM_001005201.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:55890321 C>A maps to NM_001005201.1 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr11:55890583 T>C maps to NM_001005201.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr11:55890552 G>A maps to NM_001005201.1 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr11:55889907 C>T maps to NM_001005201.1 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr11:55890129 C>T maps to NM_001005201.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr11:55890225 C>T maps to NM_001005201.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr11:55861544 G>A maps to NM_001003750.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr11:55861322 C>A maps to NM_001003750.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr11:55861031 G>T maps to NM_001003750.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:56127856 C>T maps to NM_001005205.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr11:56128489 A>G maps to NM_001005205.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr11:55904465 C>A maps to NM_001004064.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr11:55904543 A>G maps to NM_001004064.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr11:55905104 G>A maps to NM_001004064.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:56086159 C>T maps to NM_001005202.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr11:56086420 A>T maps to NM_001005202.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr11:56086350 C>G maps to NM_001005202.1 S190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr11:55927751 C>T maps to NM_001004058.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr11:55927274 G>A maps to NM_001004058.2 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr12:48919542 G>C maps to NM_001005203.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr12:48920204 C>G maps to NM_001005203.2 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr7:142724081 C>G maps to NM_001001658.1 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:141619052 C>A maps to NM_001001656.1 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr11:56468552 C>T maps to NM_001013358.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:56510366 C>T maps to NM_001005284.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:57886550 G>A maps to NM_001005211.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr12:55523875 C>T maps to NM_001005243.1 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr12:55524481 T>C maps to NM_001005243.1 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr12:55524292 G>A maps to NM_001005243.1 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:57947222 C>T maps to NM_001005212.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr11:57947257 C>G maps to NM_001005212.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:57947215 G>A maps to NM_001005212.3 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr11:57947374 C>T maps to NM_001005212.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:57958522 C>G maps to NM_001005283.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr11:57957997 C>T maps to NM_001005283.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr7:102087366 C>T maps to NM_032831.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr7:102087135 C>T maps to NM_032831.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr16:30960831 C>T maps to NM_152288.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr16:30964591 G>A maps to NM_152288.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr16:30960705 C>T maps to NM_152288.2 H32H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr16:30964570 C>T maps to NM_152288.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:69489971 C>T maps to ENST00000376587 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:52863535 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:52861994 C>T maps to NM_004153.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr6:88376825 A>T maps to NM_181837.2 T708T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr6:88321836 C>G maps to NM_181837.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr6:88315678 G>T maps to NM_181837.2 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr2:148705721 T>A maps to NM_181742.3 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr2:148705640 C>T maps to NM_181742.3 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr2:148731030 C>A maps to NM_181742.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr2:148693079 C>G maps to NM_181742.3 *437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:103848301 G>A maps to NM_002553.3 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:46729581 C>T maps to NM_014321.3 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr9:117093901 G>A maps to NM_000608.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr9:117093119 G>A maps to NM_000608.2 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:190636561 G>C maps to NM_016467.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr2:190640310 G>A maps to NM_016467.4 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:190636582 G>A maps to NM_016467.4 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:56213256 C>T maps to NM_014182.4 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:38080294 G>A maps to NM_139280.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:58114291 C>T maps to NM_006812.3 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr12:58109877 C>G maps to NM_006812.3 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr12:58088030 G>C maps to NM_006812.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:59349007 G>A maps to NM_002556.2 F566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr11:59344283 C>A maps to NM_002556.2 E759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr11:59382786 C>T maps to NM_002556.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr11:59369293 G>T maps to NM_002556.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr11:59344367 C>A maps to NM_002556.2 E731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr22:31266641 C>T maps to NM_030758.3 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr22:31289498 G>A maps to NM_030758.3 R680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr22:31285622 G>A maps to NM_030758.3 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr22:31289716 G>A maps to NM_030758.3 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:31710300 C>T maps to NM_017784.4 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr3:31921291 G>A maps to NM_017784.4 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:125257296 G>A maps to NM_022776.4 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr18:21758038 C>G maps to NM_080597.2 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr20:60868936 C>T maps to NM_144498.1 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:60835170 C>T maps to NM_144498.1 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr7:24911607 C>T maps to NM_015550.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:24843974 G>A maps to NM_015550.2 V842V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:24903174 G>C maps to NM_015550.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr7:24892221 G>T maps to NM_015550.2 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr7:24932038 G>C maps to NM_015550.2 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr11:3141764 C>T maps to NM_020896.3 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr11:3147783 C>T maps to NM_020896.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:3150276 G>A maps to NM_020896.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr2:179226524 C>T maps to ENST00000392505 R449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr2:179236857 C>G maps to ENST00000392505 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:45897372 G>A maps to NM_145798.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:45897591 G>C maps to NM_145798.2 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:45886025 C>T maps to NM_145798.2 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:45886714 C>T maps to NM_145798.2 K670K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr17:45886258 G>A maps to NM_145798.2 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr17:45886352 G>C maps to NM_145798.2 S725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr17:45894222 C>A maps to NM_145798.2 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:76788452 C>T maps to NM_020841.4 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:76763483 C>A maps to NM_020841.4 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr12:76780013 G>A maps to NM_020841.4 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:54600326 G>A maps to NM_130771.3 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr1:36898082 G>A maps to ENST00000356637 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr16:83999056 G>A maps to NM_013370.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:83999362 C>G maps to NM_013370.3 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr8:90936811 G>A maps to NM_001126111.1 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr8:90937347 C>A maps to NM_001126111.1 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr22:30659955 G>A maps to NM_020530.3 H225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr5:38884064 G>A maps to NM_003999.2 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr5:38925304 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr5:38904525 G>A maps to NM_003999.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:99961626 C>A maps to ENST00000457907 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr6:108385487 G>A maps to NM_014028.3 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:108395522 G>A maps to NM_014028.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr6:108372308 C>A maps to NM_014028.3 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr3:195953839 G>T maps to NM_152672.5 L46L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-XF-A9SP-01A-11D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr3:195955697 G>A maps to NM_152672.5 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr23:38260659 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr23:38226619 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr23:38262958 A>T did not map to a codon.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr16:21728331 T>C maps to ENST00000286149 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:21721354 C>T maps to ENST00000286149 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:21747659 C>T maps to ENST00000286149 Q808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:26703758 C>G maps to NM_194248.2 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:26739467 C>G did not map to a codon.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr2:26739407 G>A maps to NM_194248.2 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr2:26705442 C>T maps to NM_194248.2 Q470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:26706332 C>T maps to NM_194248.2 Q463Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr2:26698277 C>G maps to NM_194248.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:26706368 G>C maps to NM_194248.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr2:26702465 C>T maps to NM_194248.2 R656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:26686858 G>C maps to NM_194248.2 L1692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:161221330 C>T maps to NM_001080440.1 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr3:161221323 C>A maps to NM_001080440.1 S343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr3:161214691 A>T maps to NM_001080440.1 K33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr4:4190622 G>A maps to NM_177998.1 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr4:4190637 G>A maps to NM_177998.1 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr4:4199381 G>A maps to NM_177998.1 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:72929507 C>T maps to NM_178160.2 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:72927103 C>T maps to NM_178160.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr17:72926612 C>T maps to NM_178160.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr17:72926501 C>T maps to NM_178160.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:72938032 C>T maps to NM_178233.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr20:16729045 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr5:76932912 C>T maps to NM_032109.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:76932867 C>A maps to NM_032109.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr11:63764544 G>A maps to ENST00000422031 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr11:63764069 C>T maps to ENST00000422031 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr4:146063357 A>G maps to ENST00000447906 F604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr4:146058793 G>A maps to ENST00000447906 Q1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:146071799 G>C maps to ENST00000447906 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:48780495 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr23:48781019 G>A did not map to a codon.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr23:69283048 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr23:69282885 G>C did not map to a codon.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr23:69283219 C>T did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr23:69282756 A>T did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr23:69282407 C>G did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:69283039 G>A did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr8:92086093 G>C maps to NM_016023.3 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr15:31819388 T>A maps to ENST00000382902 K259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr15:31851253 C>T maps to ENST00000382902 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr1:149943008 G>A maps to NM_020205.2 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:149916952 G>C maps to NM_020205.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr1:149916097 G>A maps to NM_020205.2 F730F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr1:149916736 G>C maps to NM_020205.2 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr1:149915773 G>T maps to NM_020205.2 L838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:149937764 G>A maps to NM_020205.2 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr1:149916331 G>A maps to NM_020205.2 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr2:63282823 C>T maps to NM_014562.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr14:57270956 G>A maps to NM_021728.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:29604324 G>C maps to NM_183378.2 S903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr12:29596408 A>G maps to NM_183378.2 P1014P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr12:29592284 G>A maps to NM_183378.2 I1080I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr12:29608200 C>T maps to NM_183378.2 W806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:29639198 T>G maps to NM_183378.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr12:29598223 G>C maps to NM_183378.2 V956V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr12:29639256 G>C maps to NM_183378.2 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr12:29608243 C>T maps to NM_183378.2 W792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr12:29624841 G>T maps to NM_183378.2 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr12:29592299 A>G maps to NM_183378.2 F1075F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:111966265 G>A maps to ENST00000369728 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:111965673 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:111962240 G>A maps to ENST00000369728 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr11:65561514 C>T maps to NM_004561.2 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr11:65562572 C>T maps to NM_004561.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr11:65561712 G>A maps to NM_004561.2 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr20:18037359 C>A maps to NM_021220.2 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:18005306 G>A maps to NM_021220.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr20:18022274 G>C maps to NM_021220.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr20:18005585 G>A maps to NM_021220.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr5:41870448 G>C maps to NM_000436.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr5:41840600 C>T maps to NM_000436.3 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr5:41794149 C>G maps to NM_000436.3 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr5:41794170 G>C maps to NM_000436.3 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr5:41762296 C>T maps to NM_000436.3 K418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:42990185 G>A maps to NM_148962.4 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr2:42990227 G>A maps to NM_148962.4 H364H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr13:97639536 G>A maps to NM_080818.3 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr13:97639920 G>C maps to NM_080818.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr13:97639223 G>T maps to NM_080818.3 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr3:16313223 C>A maps to NM_138381.3 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr8:107718630 A>G maps to NM_001198533.1 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr8:107763045 G>A maps to NM_001198533.1 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr8:107718686 C>G maps to NM_001198533.1 S313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr8:107754478 G>A maps to NM_001198533.1 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr8:107751729 G>A maps to NM_001198533.1 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr3:38293861 T>C maps to NM_005109.2 N496N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:38292921 C>G maps to NM_005109.2 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr3:38240220 C>T maps to NM_005109.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr3:38240300 C>G maps to NM_005109.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr20:3052874 G>A maps to NM_000915.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr20:3052880 G>A maps to NM_000915.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr20:3052408 C>G maps to NM_000915.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr3:8809243 G>A maps to NM_000916.3 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:8809174 G>A maps to NM_000916.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr12:133196312 C>T maps to NM_170683.2 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FM-01A-11D-A38G-08 chr11:57114032 C>T maps to NM_002559.2 H45H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr11:57106038 C>T maps to NM_002559.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr11:57135554 C>T maps to NM_002559.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr11:57135554 C>T maps to NM_002559.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:3593965 G>A maps to ENST00000435558 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:3593443 C>T maps to ENST00000435558 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr22:21380551 C>T maps to NM_005446.3 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:21369615 C>A maps to NM_005446.3 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr22:21377686 C>T maps to NM_005446.3 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:121615183 C>T maps to NM_002562.5 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr12:121600260 G>A maps to NM_002562.5 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:121615002 C>T maps to NM_002562.5 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr3:152553927 C>T maps to NM_002563.2 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:152554518 C>T maps to NM_002563.2 N316N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:78216601 G>T did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr23:78216655 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:78216251 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:151046555 A>G maps to NM_176894.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:150931339 G>A maps to NM_014879.3 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr3:150931786 G>A maps to NM_014879.3 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr3:150931703 G>T maps to NM_014879.3 S134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:72945965 C>T maps to NM_176071.1 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:72945971 C>G maps to NM_176071.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr11:72945368 C>G maps to NM_176071.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr11:72945908 C>A maps to NM_176071.1 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr23:69478963 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr23:69479117 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr23:69479445 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr23:1585232 G>A did not map to a codon.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr23:1584476 G>C did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:1584471 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr10:74803685 C>T maps to NM_000917.3 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:74803712 C>G maps to NM_000917.3 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr5:131530658 T>A maps to NM_001142599.1 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:73997021 G>C maps to NM_182904.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:79803466 G>A maps to NM_000918.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:79817198 C>T maps to NM_000918.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr17:79804358 C>T maps to NM_000918.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:79817264 T>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr17:79813376 T>C maps to NM_000918.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:49043564 C>G maps to NM_177938.2 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:49027928 C>G maps to NM_177938.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:73627687 G>A maps to NM_025155.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr8:101721412 A>G maps to NM_002568.3 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr8:101719199 G>A maps to NM_002568.3 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr8:101717180 G>A maps to NM_002568.3 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr20:43541400 G>A maps to NM_001124756.1 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr20:43541299 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr20:43561764 C>T maps to NM_001124756.1 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr13:25671774 C>G maps to NM_030979.2 S480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr13:25671679 C>T maps to NM_030979.2 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr13:25672013 C>A maps to NM_030979.2 R560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr13:25671745 C>T maps to NM_030979.2 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:40041524 G>A maps to NM_001135653.1 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:40035344 G>A maps to NM_001135653.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr1:40034500 C>T maps to NM_001135653.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:90690801 T>C did not map to a codon.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr23:90691634 G>A did not map to a codon.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr23:90691529 G>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:90691591 A>C did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:90690846 C>T did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr11:65961018 C>G maps to NM_018026.2 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr14:105857977 C>T maps to ENST00000458164 D710D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr6:34499550 C>G maps to NM_020804.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr6:34494142 G>T maps to NM_020804.3 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:34499517 C>T maps to NM_020804.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr22:43287140 C>A maps to NM_001184970.1 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr22:43286958 C>T maps to NM_001184970.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr22:43267464 C>G maps to NM_001184970.1 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr22:43284696 G>A maps to NM_001184970.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr11:47199591 C>A maps to NM_016223.4 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr11:47200712 G>A maps to NM_016223.4 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:47202145 G>A maps to NM_016223.4 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:17552409 G>A maps to NM_013358.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:17555288 G>T maps to NM_013358.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr1:17552633 G>A maps to NM_013358.2 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr1:17557170 C>A maps to NM_013358.2 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:17395562 G>A maps to NM_007365.2 F658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:17395643 G>A maps to NM_007365.2 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:17413061 G>C maps to NM_007365.2 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:17395637 G>A maps to NM_007365.2 D633D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:17575709 C>A maps to NM_016233.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:17586129 C>T maps to NM_016233.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:17603327 G>A maps to NM_016233.2 Q504Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr1:17596740 G>A maps to NM_016233.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:17586160 G>T maps to NM_016233.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:17596866 C>A maps to NM_016233.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:17674449 C>T maps to NM_012387.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr1:17662718 C>T maps to NM_012387.2 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:17708558 G>C maps to NM_207421.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:138454264 C>T maps to NM_002571.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:39880313 G>A maps to NM_019088.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr17:2570425 C>T maps to NM_000430.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr1:26308866 C>T maps to NM_000437.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr23:49454134 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr23:49458748 G>A did not map to a codon.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr23:49597235 C>T did not map to a codon.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr23:49597170 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:55247848 G>A did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr23:55250421 G>A did not map to a codon.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr23:55247846 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:103248979 C>A maps to NM_000277.1 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr12:103271238 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:103246693 G>A maps to NM_000277.1 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr12:103246653 G>A maps to NM_000277.1 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr12:103306625 C>T maps to NM_000277.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr5:43547974 G>C maps to NM_006451.4 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:10697684 G>A maps to NM_017906.2 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:196509529 G>T maps to NM_002577.4 G5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr23:110463630 C>G did not map to a codon.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr23:110463609 C>A did not map to a codon.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr23:110439846 C>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr23:110435398 A>G did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr23:110395673 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr23:110388130 G>C did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr23:110439754 G>A did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr23:110391026 G>C did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:110406926 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr23:110406158 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr23:110366475 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:110391068 T>A did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr15:40565107 G>A maps to NM_020168.4 E466E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr15:40568154 G>T maps to NM_020168.4 E636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr15:40557006 G>A maps to NM_020168.4 K7K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr20:9520183 G>A maps to NM_177990.2 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr20:9561535 G>A maps to NM_177990.2 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr16:23641637 G>A maps to NM_024675.3 Q613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr16:23647422 C>T maps to NM_024675.3 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr16:23646594 G>C maps to NM_024675.3 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:169602527 C>G maps to NM_001166108.1 S378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr4:169602522 C>T maps to NM_001166108.1 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr4:169819675 C>G maps to NM_001166108.1 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:746780 G>A maps to NM_002579.2 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr9:112924402 G>A maps to NM_007203.4 V1068V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr5:102360916 G>A maps to NM_000919.3 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:35492233 G>A maps to NM_015430.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr11:35515734 G>A maps to NM_015430.2 C53C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr12:56712105 G>A maps to NM_001127460.2 F1163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr12:56720612 A>G maps to NM_001127460.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:56722296 G>A maps to NM_001127460.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:56717845 G>C maps to NM_001127460.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:56715865 C>T maps to NM_001127460.2 L932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr12:56721347 G>C maps to NM_001127460.2 S240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr12:56720471 G>A maps to NM_001127460.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr12:56720453 G>A maps to NM_001127460.2 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr13:28844907 T>C maps to NM_175854.7 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr10:91359178 G>A maps to NM_148977.1 N380N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr10:91371548 G>A maps to NM_148977.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr10:91348516 C>A maps to NM_148977.1 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr10:91404996 A>G maps to NM_148977.1 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr10:91371743 C>T maps to NM_148977.1 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr20:3888747 C>T maps to NM_153638.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:3891267 G>A maps to NM_153638.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr20:3870271 C>A maps to NM_153638.2 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr20:3869935 G>A maps to NM_153638.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:167993163 A>G maps to NM_024594.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr5:167986162 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:168006267 C>T maps to NM_024594.2 K7K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr5:167988433 G>A maps to NM_024594.2 N300N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:2452341 G>A maps to ENST00000425477 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:2447126 C>T maps to ENST00000425477 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:2452164 C>T maps to ENST00000425477 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:93912932 C>T maps to NM_015368.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr22:50609336 C>T maps to NM_052839.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr22:50617583 G>T maps to NM_052839.3 E638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:124482953 C>A maps to NM_052959.2 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr11:124482882 G>A maps to NM_052959.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr11:124482879 T>C maps to NM_052959.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr11:124489536 T>C maps to NM_052959.2 C295C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr11:124481613 C>T maps to NM_052959.2 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr10:135204913 C>T maps to NM_152911.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr10:135197563 C>T maps to NM_152911.2 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr10:135202546 C>T maps to NM_152911.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr10:135195128 C>T maps to NM_152911.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr5:78915519 C>T maps to NM_173797.3 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr5:78964812 C>G maps to NM_173797.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr5:78915519 C>T maps to NM_173797.3 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:78944940 C>T maps to NM_173797.3 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr5:78936675 G>A maps to NM_173797.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr5:6750552 C>T maps to NM_006999.4 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr5:6743868 C>T maps to NM_006999.4 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr5:6751219 C>T maps to NM_006999.4 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr19:39591411 C>T maps to NM_001004318.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr14:73735300 C>T maps to ENST00000427855 V1179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr14:73712861 C>A maps to ENST00000427855 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr14:97009194 C>A maps to NM_032632.3 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr7:4900820 T>A maps to NM_020144.4 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr7:4900355 G>C maps to NM_020144.4 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr9:118982271 C>T maps to NM_002581.3 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr9:118950123 G>A maps to NM_002581.3 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr9:118982345 C>A maps to NM_002581.3 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr9:119097188 C>G maps to NM_002581.3 V1149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr1:176659487 G>T maps to NM_020318.2 E785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:176525733 A>T maps to NM_020318.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:176564282 G>T maps to NM_020318.2 G515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:176659423 A>G maps to NM_020318.2 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr1:176759079 G>A maps to NM_020318.2 Q1617Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:176659285 C>T maps to NM_020318.2 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr1:176526019 C>T maps to NM_020318.2 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr1:176740226 C>G maps to NM_020318.2 L1542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr1:176563771 C>T maps to NM_020318.2 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr1:176525626 C>A maps to NM_020318.2 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr4:108614974 T>C maps to NM_005443.4 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr4:108552815 C>T maps to NM_005443.4 K569K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr10:89504907 C>T maps to NM_001015880.1 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:89472928 C>G maps to NM_001015880.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:89501081 C>T maps to NM_001015880.1 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr4:79860219 G>T maps to NM_001040202.1 Y53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr16:3019836 G>C maps to NM_152341.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr16:3021897 C>T maps to NM_152341.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr16:3021374 C>T maps to NM_152341.3 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr15:69682008 C>T maps to NM_017705.3 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr15:69677201 C>T maps to NM_017705.3 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr15:69677080 G>A maps to NM_017705.3 W82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr15:69692414 C>T maps to NM_017705.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:156214584 C>A maps to NM_024897.2 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:156213681 C>G maps to NM_024897.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:26189907 C>T maps to NM_178422.5 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:26190183 C>T maps to NM_178422.5 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:26189742 C>T maps to NM_178422.5 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:52268301 C>T maps to ENST00000361841 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr6:52268631 C>T maps to ENST00000361841 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:52268221 C>T maps to ENST00000361841 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr3:142681209 G>A maps to NM_198504.2 Y323Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:142682016 G>A maps to NM_198504.2 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:142681983 A>T maps to NM_198504.2 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr3:142681683 G>C maps to NM_198504.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:34420502 G>C maps to NM_019619.3 S1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:34648121 C>A maps to NM_019619.3 G674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:34688321 C>A maps to NM_019619.3 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:34558669 G>A maps to NM_019619.3 Q1115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr10:34626229 G>A maps to NM_019619.3 R848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr10:34805960 G>A maps to NM_019619.3 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr10:34805960 G>A maps to NM_019619.3 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr10:35103842 G>A maps to NM_019619.3 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr10:34759173 G>A maps to NM_019619.3 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr10:34636905 G>A maps to NM_019619.3 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:206023471 C>G maps to ENST00000406610 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:206023537 C>A maps to ENST00000406610 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:206166206 C>T maps to ENST00000406610 S804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr2:205990385 C>T maps to ENST00000406610 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:206480356 G>A maps to ENST00000406610 P1146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:205990412 A>C maps to ENST00000406610 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr16:67695397 C>A maps to NM_016948.2 S35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr16:67696108 G>C maps to NM_016948.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr16:67696466 C>T maps to NM_016948.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr16:67695398 G>A maps to NM_016948.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr20:49354430 C>G maps to NM_032521.2 S35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:51065369 C>A maps to NM_003631.2 E779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr6:162864341 C>T maps to NM_004562.2 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr6:162683620 A>G maps to NM_004562.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr6:161807841 G>T maps to NM_004562.2 S384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr1:8025424 A>G maps to NM_001123377.1 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:14676059 G>A maps to NM_002582.2 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr16:14704554 G>C maps to NM_002582.2 S167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:226567865 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:226589953 G>A maps to NM_001618.3 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:226555920 C>T maps to NM_001618.3 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr1:226570803 G>A maps to NM_001618.3 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr1:226549208 C>T maps to NM_001618.3 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr8:145060241 G>A maps to NM_032789.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr8:145052105 G>A maps to NM_032789.3 H900H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr8:145057979 C>T did not map to a codon.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr8:145060235 G>A maps to NM_032789.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr7:139754464 G>A maps to NM_022750.2 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr3:122446796 C>T maps to NM_017554.2 R1694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr3:122433110 C>T maps to NM_017554.2 Q1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr3:122437552 C>T maps to NM_017554.2 R1519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr3:122399789 G>T maps to NM_017554.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr3:122437770 C>T maps to NM_017554.2 H1591H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr3:122418708 A>T maps to NM_017554.2 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:122418337 A>T maps to NM_017554.2 K313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr3:122419062 C>T maps to NM_017554.2 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr3:122354757 C>A maps to NM_001113523.1 Y616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr3:122354000 C>G maps to NM_001113523.1 V569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:122354847 C>G maps to NM_001113523.1 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr3:122345779 C>T maps to NM_001113523.1 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr15:65555625 G>T maps to NM_017851.4 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr15:65578617 G>A maps to NM_017851.4 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr3:51979110 G>A maps to NM_001003931.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:51978421 C>G maps to NM_001003931.2 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr3:51979098 G>C maps to NM_001003931.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:25067845 G>C maps to NM_006437.3 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr13:25074458 G>A maps to NM_006437.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr13:25029218 G>A maps to NM_006437.3 I898I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr13:25008865 C>T maps to NM_006437.3 L1471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr13:25009315 C>T maps to NM_006437.3 P1321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr13:25029182 C>T maps to NM_006437.3 Q910Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr15:72533822 C>T maps to NM_020214.2 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr15:72558266 C>T maps to NM_020214.2 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr15:72552920 C>T maps to NM_020214.2 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr5:50137808 C>T maps to ENST00000505697 D825D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr5:50090119 G>T maps to ENST00000505697 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr5:50057698 C>T maps to ENST00000505697 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr5:50093021 G>A maps to ENST00000505697 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr5:50073936 C>T maps to ENST00000505697 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr5:50058989 T>C maps to ENST00000505697 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr5:50118183 C>A maps to ENST00000505697 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr3:122277248 C>T maps to NM_031458.2 Q27Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr3:122259409 G>T maps to NM_031458.2 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr3:122259633 G>A maps to NM_031458.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr3:122269627 C>A maps to NM_031458.2 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr1:55223754 A>G maps to NM_152268.3 C360C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr11:12525870 C>T maps to NM_018222.4 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:12518095 C>T maps to NM_018222.4 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr22:44532338 G>A did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr22:44514967 G>A maps to NM_001003828.1 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr22:44395508 C>G maps to NM_001003828.1 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr22:44585084 G>A maps to NM_001137606.1 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr22:44601698 C>G maps to NM_001137606.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr22:44581704 C>T maps to NM_001137606.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr22:44584994 G>A maps to NM_001137606.1 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr22:44585036 G>C maps to NM_001137606.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr23:150832622 G>A did not map to a codon.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr23:150840121 A>G did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr23:150793932 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:150842432 G>T did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:150842565 G>C did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr2:242063471 G>A maps to ENST00000358649 L932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:242066100 G>C maps to ENST00000358649 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:242072386 C>G maps to ENST00000358649 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr2:242065893 C>T maps to ENST00000358649 R812R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr2:242046891 C>T maps to ENST00000358649 G1237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr2:242076583 C>A maps to ENST00000358649 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:242046914 C>G did not map to a codon.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr11:125617634 C>T maps to NM_138294.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr11:125648650 G>C maps to NM_212555.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr11:59406551 G>A maps to NM_152716.2 Q754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr11:59415361 C>T maps to NM_152716.2 Q586Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:31738884 G>A maps to NM_014323.2 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr22:31741456 G>A maps to NM_014323.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr22:31723200 C>T maps to NM_014323.2 Q580Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr22:31731849 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr22:31741098 G>A maps to NM_014323.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr12:79986469 G>A maps to NM_002583.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr20:21687181 C>T maps to NM_006192.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr10:102541060 C>T maps to NM_003987.3 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr10:102509527 C>T maps to NM_003987.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr10:102510507 G>A maps to NM_003987.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr10:102568919 G>C maps to NM_003987.3 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr2:223161756 C>A maps to NM_181459.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr2:223085953 T>C maps to NM_181459.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr2:223096986 G>C maps to NM_181459.3 S201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr2:223085998 C>T maps to NM_181459.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:223161714 G>A maps to NM_181459.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr7:127251628 C>T maps to NM_006193.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr7:127252025 C>T maps to NM_006193.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr9:37015061 G>A maps to NM_016734.1 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:36966698 C>G maps to NM_016734.1 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:31823445 T>A maps to NM_001604.4 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr11:31824257 A>T maps to NM_001604.4 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:31811519 C>A maps to NM_001604.4 E425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr1:19029750 C>T maps to NM_002584.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:19018371 G>A maps to NM_002584.2 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:18960998 C>T maps to NM_002584.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr2:114002098 C>T maps to NM_003466.3 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:113993004 C>G maps to NM_003466.3 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr14:37145474 C>T maps to NM_006194.3 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr14:37132475 C>T maps to NM_006194.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr7:154746076 G>A maps to NM_007349.3 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr10:70044040 G>A maps to NM_022129.3 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr10:70048776 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr3:52678806 T>C did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:52582189 C>T maps to ENST00000296302 L1653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:52621526 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr3:52582215 C>A maps to ENST00000296302 E1645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:52696217 C>T maps to ENST00000296302 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr3:52621368 C>T maps to ENST00000296302 K1041K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr6:32154670 G>A maps to NM_002586.4 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr6:32156276 G>A maps to NM_002586.4 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr9:128677987 G>T maps to ENST00000373487 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr1:154918383 G>C maps to NM_020524.2 S589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr11:66631397 G>T maps to NM_022172.2 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr11:66636333 G>A maps to NM_022172.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:66619973 G>C maps to NM_022172.2 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:66617711 C>T maps to NM_022172.2 Q899Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr11:66636411 G>C maps to NM_022172.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:66619931 G>C maps to NM_022172.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr5:134296289 C>T maps to NM_032151.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:70315789 C>T maps to NM_006196.3 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:53858605 C>T maps to NM_005016.5 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr21:47359996 G>A maps to NM_020528.2 Q321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr21:47330883 C>T maps to NM_020528.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr21:47349883 C>G maps to NM_020528.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr3:51993934 G>A maps to NM_033010.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:136045669 G>C maps to NM_001178014.1 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:135974723 C>A maps to NM_001178014.1 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr3:136002773 C>T maps to NM_001178014.1 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:141244800 G>A maps to NM_032420.2 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr5:141248532 G>A maps to NM_032420.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr5:141244389 G>A maps to NM_032420.2 N502N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr4:134072902 G>A maps to NM_032961.1 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr4:134071561 C>A maps to NM_032961.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr4:134073853 C>T maps to NM_032961.1 C853C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr4:134071537 C>T maps to NM_032961.1 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr4:134072296 C>T maps to NM_032961.1 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr4:134073226 C>A maps to NM_032961.1 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr4:134073496 C>T maps to NM_032961.1 I734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr4:134072395 G>A maps to NM_032961.1 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:134071783 C>T maps to NM_032961.1 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr4:134072434 C>T maps to NM_032961.1 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr4:134071765 C>T maps to NM_032961.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:91134183 C>T did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr23:91137941 G>A did not map to a codon.
Sequencing variant TCGA-CF-A9FH-01A-11D-A38G-08 chr23:91134044 G>T did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr23:91132784 G>C did not map to a codon.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr23:91090514 G>T did not map to a codon.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr23:91873849 A>T did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:91873588 C>T did not map to a codon.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr23:91131935 G>T did not map to a codon.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr23:91873796 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr23:91642792 T>A did not map to a codon.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr23:91132443 A>G did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:91131908 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:91131799 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr23:91873529 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr24:4968462 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr24:4925108 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr24:4968403 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr24:4968691 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr24:4968708 G>T did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr24:4967172 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr24:4968003 C>T did not map to a codon.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr24:4966475 T>C did not map to a codon.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr24:4968261 G>T did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr24:4968271 G>C did not map to a codon.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr24:4968031 A>T did not map to a codon.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr24:4968033 T>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:141325350 C>T maps to NM_016580.2 L1050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr5:141335103 C>T maps to NM_016580.2 Q771Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr5:141335208 G>A maps to NM_016580.2 F736F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr5:141335010 C>T maps to NM_016580.2 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr5:141325350 C>T maps to NM_016580.2 L1050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr5:141324963 G>A maps to NM_016580.2 S1179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr10:55583057 C>T maps to NM_001142763.1 R1483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:55826640 G>C maps to NM_001142763.1 S704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr10:55566553 G>A maps to ENST00000373965 L1614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr10:55626578 G>T maps to NM_001142763.1 A1185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr10:55582247 G>T maps to NM_001142763.1 P1753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr10:56287570 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr10:56077150 T>G maps to NM_001142763.1 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr10:55996676 G>A maps to NM_001142763.1 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr10:55569090 G>A maps to NM_001142769.1 R1578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr10:55582796 C>T maps to NM_001142763.1 L1570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr10:55569096 C>T maps to NM_001142769.1 Q1576Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr13:58207744 C>T maps to NM_001040429.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr13:58208644 G>A maps to NM_001040429.2 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr13:58207696 C>G maps to NM_001040429.2 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr13:58207318 G>A maps to NM_001040429.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr13:58298980 C>A maps to NM_001040429.2 L1011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr13:58208005 C>T maps to NM_001040429.2 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr13:58207297 G>A maps to NM_001040429.2 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr13:58299355 G>A maps to NM_001040429.2 E1136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr13:58298894 G>T maps to NM_001040429.2 E983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr13:58299226 C>T maps to NM_001040429.2 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr4:138449706 G>T maps to NM_019035.3 R889R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr4:138442251 G>A maps to NM_019035.3 H1113H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr23:99661762 G>A did not map to a codon.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr23:99661859 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr23:99663457 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:99661855 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:99662547 A>G did not map to a codon.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr23:99551498 G>C did not map to a codon.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr23:99662754 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:99663575 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr23:99663096 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr23:99662866 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:99551335 A>T did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:99551481 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr23:99662021 T>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr23:99662161 G>A did not map to a codon.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr13:61985376 C>G maps to NM_022843.3 *952S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr13:61987634 G>A maps to NM_022843.3 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr13:61987748 C>T maps to NM_022843.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr13:61987072 C>A maps to NM_022843.3 G387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr13:61986121 G>A maps to NM_022843.3 Q704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr13:61987370 C>G maps to NM_022843.3 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr13:61987205 G>C maps to NM_022843.3 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr4:30723145 C>A maps to NM_001173523.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:30725716 G>T maps to NM_001173523.1 V891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr4:30724468 C>T maps to NM_001173523.1 D475D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr4:30724738 T>C maps to NM_001173523.1 G565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr4:31144158 C>T maps to NM_001173523.1 G1152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr13:53421521 G>A maps to NM_002590.2 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr13:53421107 G>A maps to NM_002590.2 G488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr13:53422430 C>T maps to NM_002590.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr13:53420644 C>A maps to NM_002590.2 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr13:53420939 G>A maps to NM_002590.2 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr13:53420309 G>A maps to NM_002590.2 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr13:67799770 G>A maps to NM_203487.2 D934D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:67802499 C>A maps to NM_203487.2 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr13:67800922 A>T maps to NM_203487.2 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr13:66878786 T>G maps to NM_203487.2 *1238Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr13:67477694 G>A maps to NM_203487.2 Q1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr13:67801585 T>C maps to NM_203487.2 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr13:67477694 G>A maps to NM_203487.2 Q1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr13:67800823 C>T maps to NM_203487.2 E583E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr13:67799728 A>G maps to NM_203487.2 F948F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr13:67799572 T>A maps to NM_203487.2 G1000G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr13:66878834 A>C maps to NM_203487.2 Y1222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr5:140167230 G>A maps to NM_018900.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:140167236 G>A maps to NM_018900.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:140166573 C>T maps to NM_018900.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr5:140166573 C>T maps to NM_018900.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr5:140166543 A>G maps to NM_018900.2 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr5:140166144 C>T maps to NM_018900.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr5:140166708 C>G maps to NM_018900.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr5:140167059 C>T maps to NM_018900.2 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SU-01A-31D-A391-08 chr5:140167908 G>A maps to NM_018900.2 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SU-01A-31D-A391-08 chr5:140168076 G>A maps to NM_018900.2 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr5:140167203 G>A maps to NM_018900.2 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr5:140236794 C>T maps to NM_018901.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr5:140236436 G>A maps to NM_018901.2 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr5:140237279 G>A maps to NM_018901.2 T549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr5:140237300 C>T maps to NM_018901.2 D556D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr5:140237531 G>A maps to NM_018901.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr5:140236145 C>G maps to NM_018901.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr5:140249092 C>G maps to NM_018902.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr5:140249820 C>G maps to NM_018902.3 S378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr5:140250646 C>T maps to NM_018902.3 H653H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr5:140250982 G>A maps to NM_018902.3 K765K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:140256019 C>T maps to NM_018903.2 N321N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr5:140255527 T>C maps to NM_018903.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr5:140257162 C>A maps to NM_018903.2 I702I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr5:140257093 G>A maps to NM_018903.2 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr5:140257234 G>A maps to NM_018903.2 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:140256124 G>A maps to NM_018903.2 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr5:140255134 G>T maps to NM_018903.2 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr5:140255206 G>A maps to NM_018903.2 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr5:140257036 G>A maps to NM_018903.2 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr5:140257348 G>A maps to NM_018903.2 P764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr5:140257195 C>T maps to NM_018903.2 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr5:140256727 C>T maps to NM_018903.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr5:140262035 G>A maps to NM_018904.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr5:140262122 C>T maps to NM_018904.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr5:140263523 C>T maps to NM_018904.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr5:140264081 C>T maps to NM_018904.2 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:140262518 G>A maps to NM_018904.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:140261939 C>A maps to NM_018904.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr5:140264042 C>T maps to NM_018904.2 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr5:140263967 C>T maps to NM_018904.2 C705C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr5:140262974 G>T maps to NM_018904.2 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr5:140263637 C>T maps to NM_018904.2 R595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr5:140263625 G>T maps to NM_018904.2 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr5:140261996 C>T maps to NM_018904.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr5:140175343 C>T maps to NM_018905.2 N265N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr5:140175187 G>T maps to NM_018905.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:140175307 G>A maps to NM_018905.2 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr5:140176084 G>A maps to NM_018905.2 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr5:140175217 G>A maps to NM_018905.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr5:140176614 C>G maps to NM_018905.2 S689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:140176231 C>T maps to NM_018905.2 N561N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr5:140175540 C>G maps to NM_018905.2 S331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr5:140176660 C>T maps to NM_018905.2 I704I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr5:140175754 G>A maps to NM_018905.2 K402K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr5:140175794 G>T maps to NM_018905.2 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr5:140182068 C>T maps to NM_018906.2 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr5:140182065 G>A maps to NM_018906.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr5:140188544 G>A maps to NM_018907.2 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:140188376 G>T maps to NM_018907.2 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr5:140188481 G>T maps to NM_018907.2 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr5:140188691 G>A maps to NM_018907.2 T640T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr5:140187571 C>G maps to NM_018907.2 S267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr5:140186930 A>G maps to NM_018907.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr5:140187629 G>A maps to NM_018907.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr5:140188973 G>A maps to NM_018907.2 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr5:140188664 C>T maps to NM_018907.2 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr5:140187476 C>A maps to NM_018907.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr5:140203330 G>A maps to NM_018908.2 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr5:140202694 C>A maps to NM_018908.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr5:140201626 C>T maps to NM_018908.2 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr5:140203411 C>T maps to NM_018908.2 G684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr5:140209295 G>A maps to NM_018909.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr5:140209469 C>T maps to NM_018909.2 D598D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr5:140209958 G>A maps to NM_018909.2 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr5:140209055 C>A maps to NM_018909.2 Y460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr5:140209724 G>A maps to NM_018909.2 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:140209835 G>A maps to NM_018909.2 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr5:140209922 G>A maps to NM_018909.2 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr5:140209202 G>A maps to NM_018909.2 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr5:140214294 C>T maps to NM_018910.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr5:140216028 A>T maps to NM_018910.2 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr5:140216196 C>T maps to NM_018910.2 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr5:140214243 C>G maps to NM_018910.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr5:140215821 G>C maps to NM_018910.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr5:140215432 C>T maps to NM_018910.2 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr5:140214159 C>T maps to NM_018910.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr5:140222621 C>A maps to NM_018911.2 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:140222357 G>A maps to NM_018911.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:140220968 C>G maps to NM_018911.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr5:140222771 C>T maps to NM_018911.2 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr5:140222945 G>A maps to NM_018911.2 S680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr5:140221040 G>A maps to NM_018911.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr5:140222441 G>A maps to NM_018911.2 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr5:140230218 C>T maps to NM_031857.1 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr5:140228355 C>G maps to NM_031857.1 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr5:140228250 G>A maps to NM_031857.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr5:140230131 G>T maps to NM_031857.1 V684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr5:140229588 G>A maps to NM_031857.1 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:140308754 C>T maps to NM_018898.3 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr5:140306725 C>T maps to NM_018898.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr5:140347511 C>T maps to NM_018899.5 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr5:140347703 C>T maps to NM_018899.5 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr5:140348366 C>T maps to NM_018899.5 A672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr5:140347070 G>A maps to NM_018899.5 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:140346656 C>T maps to NM_018899.5 N102N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr5:140348666 C>G maps to NM_018899.5 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr5:140348888 C>G maps to NM_018899.5 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr5:140348519 C>T maps to NM_018899.5 I723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:140348185 C>A maps to NM_018899.5 S612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr5:140348111 G>A maps to NM_018899.5 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr5:140346830 G>A maps to NM_018899.5 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr5:140431441 T>C maps to NM_013340.2 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:140431477 G>A maps to NM_013340.2 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:140432122 C>A maps to NM_013340.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr5:140432012 C>T maps to NM_013340.2 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr5:140431522 C>T maps to NM_013340.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr5:140432473 A>G maps to NM_013340.2 K473K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr5:140431066 G>A maps to NM_013340.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr5:140432458 G>A maps to NM_013340.2 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:140574095 G>A maps to NM_018930.3 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr5:140574146 G>A maps to NM_018930.3 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr5:140573672 C>T maps to NM_018930.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr5:140572550 A>T maps to NM_018930.3 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr5:140573591 G>A maps to NM_018930.3 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:140580554 T>A maps to NM_018931.2 L403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr5:140581594 C>T maps to NM_018931.2 Q750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr5:140580723 C>T maps to NM_018931.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:140589000 G>A maps to NM_018932.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr5:140589324 C>A maps to NM_018932.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr5:140590299 C>G maps to NM_018932.3 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr5:140589141 C>T maps to NM_018932.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr5:140589927 C>T maps to NM_018932.3 N483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr5:140590335 G>A maps to NM_018932.3 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr5:140588551 C>T maps to NM_018932.3 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr5:140590224 G>T maps to NM_018932.3 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr5:140590431 G>T maps to NM_018932.3 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr5:140590501 G>T maps to NM_018932.3 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr5:140590575 G>A maps to NM_018932.3 S699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr5:140589000 G>A maps to NM_018932.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:140594402 C>T maps to NM_018933.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:140594618 C>T maps to NM_018933.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr5:140595314 G>A maps to NM_018933.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr5:140594717 G>A maps to NM_018933.2 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr5:140594771 G>A maps to NM_018933.2 E359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr5:140604576 C>A maps to NM_018934.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr5:140604417 C>T maps to NM_018934.2 N447N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr5:140605047 G>A maps to NM_018934.2 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr5:140626594 C>T maps to NM_018935.2 N483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr5:140626624 C>G maps to NM_018935.2 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr5:140627248 C>T maps to NM_018935.2 F701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr5:140627002 G>A maps to NM_018935.2 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr5:140563414 G>A maps to NM_020957.1 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr5:140563663 C>T maps to NM_020957.1 N510N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr5:140563169 C>T maps to NM_020957.1 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:140562148 G>A maps to NM_020957.1 W5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr5:140564191 C>G maps to NM_020957.1 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr5:140562364 C>T maps to NM_020957.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr5:140564296 G>A maps to NM_020957.1 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr5:140475831 C>G maps to NM_018936.2 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr5:140475030 C>T maps to NM_018936.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr5:140474488 G>T maps to NM_018936.2 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr5:140475033 G>C maps to NM_018936.2 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr5:140481939 C>T maps to NM_018937.2 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:140482300 C>T maps to NM_018937.2 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr5:140480520 C>T maps to NM_018937.2 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr5:140481672 A>G maps to NM_018937.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr5:140482029 C>T maps to NM_018937.2 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr5:140480868 C>T maps to NM_018937.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr5:140503378 G>A maps to NM_018938.2 W600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr5:140517124 G>A maps to NM_015669.2 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr5:140517288 C>G maps to NM_015669.2 S758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr5:140516524 C>T maps to NM_015669.2 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr5:140516731 C>A maps to NM_015669.2 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr5:140516902 G>T maps to NM_015669.2 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr5:140516512 C>A maps to NM_015669.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr5:140516662 G>A maps to NM_015669.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr5:140515517 C>T maps to NM_015669.2 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr5:140516635 G>A maps to NM_015669.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr5:140530227 G>A maps to NM_018939.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr5:140532169 G>T maps to NM_018939.2 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr5:140530311 T>C maps to NM_018939.2 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:140530833 C>T maps to NM_018939.2 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr5:140531691 C>T maps to NM_018939.2 H618H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr5:140529850 A>T maps to NM_018939.2 K5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr5:140532099 G>A maps to NM_018939.2 T754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:140553777 C>A maps to NM_018940.2 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr5:140553171 C>T maps to NM_018940.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr5:140553672 C>T maps to NM_018940.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr5:140552991 C>G maps to NM_018940.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr5:140553378 C>T maps to NM_018940.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr5:140554035 G>T maps to NM_018940.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr5:140554036 C>T maps to NM_018940.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr5:140554488 G>A maps to NM_018940.2 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr5:140552931 C>T maps to NM_018940.2 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr5:140559117 C>T maps to NM_019120.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr5:140558076 T>A maps to NM_019120.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:140559207 G>C maps to NM_019120.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr5:140559900 G>A maps to NM_019120.2 T762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:140558544 C>T maps to NM_019120.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr5:140559003 G>A maps to NM_019120.2 E463E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr5:140559507 G>A maps to NM_019120.2 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr5:140559549 C>G maps to NM_019120.2 V645V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr5:140558694 T>C maps to NM_019120.2 N360N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr5:140558397 G>C maps to NM_019120.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr5:140558160 C>T maps to NM_019120.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:140712086 C>T maps to NM_018912.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr5:140710505 C>T maps to NM_018912.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr5:140710706 C>G maps to NM_018912.2 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr5:140710880 C>T maps to NM_018912.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr5:140712347 G>T maps to NM_018912.2 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr5:140711155 C>G maps to NM_018912.2 S302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr5:140711933 G>A maps to NM_018912.2 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr5:140890658 C>T maps to NM_018915.2 N906N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr5:140710946 G>T maps to NM_018912.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr5:140712278 C>A maps to NM_018912.2 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr5:140710643 C>A maps to NM_018912.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr5:140711155 C>G maps to NM_018912.2 S302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr5:140711876 C>T maps to NM_018912.2 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr5:140794088 C>T maps to NM_018913.2 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr5:140794859 C>T maps to NM_018913.2 C706C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr5:140793095 G>A maps to NM_018913.2 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:140793479 C>T maps to NM_018913.2 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr5:140794340 G>A maps to NM_018913.2 Q533Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr5:140811993 C>T maps to NM_003735.2 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr5:140811699 C>T maps to NM_003735.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr5:140810373 G>A maps to NM_003735.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr5:140811615 G>A maps to NM_003735.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr5:140811519 C>T maps to NM_003735.2 Y398Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr5:140720871 G>A maps to NM_018915.2 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr5:140720803 G>T maps to NM_018915.2 E756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr5:140720478 G>A maps to NM_018915.2 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr5:140719539 C>T maps to NM_018915.2 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr5:140719674 C>T maps to NM_018915.2 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr5:140720340 C>T maps to NM_018915.2 N601N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr5:140718831 G>A maps to NM_018915.2 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr5:140720763 C>T maps to NM_018915.2 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr5:140725378 G>A maps to NM_018916.3 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:140724215 G>T maps to NM_018916.3 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr5:140725933 G>A maps to NM_018916.3 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr5:140725894 G>A maps to NM_018916.3 K765K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr5:140724205 T>G maps to NM_018916.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAME-01A-12D-A42E-08 chr5:140725810 C>T maps to NM_018916.3 G737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:140736302 G>A maps to NM_018917.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr5:140736326 C>T maps to NM_018917.2 F520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr5:140737032 G>T maps to NM_018917.2 E756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr5:140745831 C>G maps to NM_018918.2 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr5:140745564 C>T maps to NM_018918.2 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr5:140745456 C>T maps to NM_018918.2 F520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr5:140745615 G>A maps to NM_018918.2 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr5:140745834 C>T maps to NM_018918.2 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:140753991 G>A maps to NM_018919.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:140753781 C>T maps to NM_018919.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr5:140755383 G>C maps to NM_018919.2 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr5:140754642 G>T maps to NM_018919.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr5:140755944 G>A maps to NM_018919.2 K765K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr5:140755098 G>A maps to NM_018919.2 Q483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:140763129 C>T maps to NM_018920.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr5:140764039 T>A maps to NM_018920.2 L525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr5:140764091 C>T maps to NM_018920.2 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr5:140763838 C>G maps to NM_018920.2 S458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr5:140774632 G>A maps to NM_032088.1 Q751Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr5:140773777 G>C maps to NM_032088.1 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr5:140774318 C>T maps to NM_032088.1 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr5:140783886 C>T maps to NM_018921.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr5:140784366 C>T maps to NM_018921.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:140784666 G>T maps to NM_018921.2 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr5:140782947 C>T maps to NM_018921.2 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:140730186 C>T maps to NM_018922.2 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr5:140730096 G>A maps to NM_018922.2 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:140730574 G>T maps to NM_018922.2 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr5:140730189 A>G maps to NM_018922.2 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr5:140741705 G>C maps to NM_018923.2 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr5:140739725 C>T maps to NM_018923.2 C8C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr5:140740853 C>T maps to NM_018923.2 C384C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr5:140740784 A>G maps to NM_018923.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr5:140750326 G>A maps to NM_018924.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr5:140750854 G>A maps to NM_018924.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr5:140751512 C>T maps to NM_018924.2 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr5:140750462 C>T maps to NM_018924.2 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr5:140751880 G>A maps to NM_018924.2 Q640Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr5:140751745 C>T maps to NM_018924.2 D595D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr5:140769061 G>A maps to NM_003736.2 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr5:140768431 G>A maps to NM_003736.2 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:140769070 C>G maps to NM_003736.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr5:140768962 C>A maps to NM_003736.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr5:140768263 G>A maps to NM_003736.2 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr5:140799084 C>T maps to NM_018927.2 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr5:140797677 A>G maps to NM_018927.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr5:140855724 G>C maps to NM_002588.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr5:140865369 G>A maps to NM_018928.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr5:140866532 T>A maps to NM_018928.2 L598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr5:140868824 C>G maps to NM_018929.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr5:140870915 C>G maps to NM_018929.2 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr2:120404545 C>T maps to NM_001029996.3 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:120385259 G>C maps to NM_001029996.3 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:120395872 G>C maps to NM_001029996.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr11:82877652 C>T maps to NM_015885.3 Q572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:82877724 A>C maps to NM_015885.3 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr11:82879568 C>G maps to NM_015885.3 S731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:82879594 C>T maps to NM_015885.3 Q740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:82877030 G>A maps to NM_015885.3 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr11:82880299 C>T maps to NM_015885.3 Q975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr11:82877285 C>A maps to NM_015885.3 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr17:36895327 C>A maps to NM_007144.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr10:105110682 A>C maps to NM_001011663.1 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr13:113862924 C>T maps to ENST00000246505 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr13:113834319 C>T maps to ENST00000246505 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr20:44571880 C>T maps to NM_022104.3 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr20:44569784 C>G maps to NM_022104.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:44573622 G>C maps to NM_022104.3 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:44574945 C>T maps to NM_022104.3 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr20:44569552 C>T maps to NM_022104.3 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr20:44567878 G>A maps to NM_022104.3 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:56136481 G>A maps to NM_002591.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr20:56140583 A>G maps to NM_002591.3 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr7:82584310 C>T maps to NM_033026.5 Q1986Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr7:82451793 T>G maps to NM_014510.2 *4936Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:82579160 C>T maps to NM_033026.5 L3581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:82585599 G>A maps to NM_033026.5 R1557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr7:82544281 G>T maps to NM_033026.5 T4340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr7:82595457 C>A maps to NM_033026.5 E1216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:82390089 C>G maps to NM_033026.5 V5051V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr7:82763760 A>G maps to NM_033026.5 S1035S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr7:82545847 C>T maps to NM_033026.5 K3818K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr7:82585933 C>T maps to NM_033026.5 Q1445Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr7:82585918 C>T maps to NM_033026.5 E1450E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr7:82581328 C>T maps to NM_033026.5 G2980G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr7:82581178 A>T maps to NM_033026.5 V3030V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr7:82585069 T>C maps to NM_033026.5 S1733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:82583805 C>A maps to NM_033026.5 E2155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr7:82764882 C>T maps to NM_033026.5 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr7:82583254 G>A maps to NM_033026.5 T2338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:82785626 G>C maps to NM_033026.5 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr8:17813069 C>T maps to NM_006197.3 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:150094289 C>T maps to NM_005389.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:52733176 G>A maps to NM_052937.2 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr8:52773483 C>T maps to NM_052937.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr20:62899363 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr20:62896742 C>T maps to NM_018257.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr20:5096164 C>T maps to NM_002592.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:101311590 C>T maps to NM_020357.1 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr3:101304279 G>C did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr21:47746352 G>A maps to NM_006031.5 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr21:47858171 G>A maps to NM_006031.5 E3065E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr21:47850002 G>A maps to NM_006031.5 E2590E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr21:47851759 G>A maps to NM_006031.5 L2794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:47769078 C>T maps to NM_006031.5 Q396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:47810623 G>T maps to NM_006031.5 E1294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr21:47787023 C>G maps to NM_006031.5 T1045T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr21:47821561 C>A maps to NM_006031.5 S1630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr21:47769712 C>T maps to NM_006031.5 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr21:47847642 C>T maps to NM_006031.5 L2476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr21:47809234 C>T maps to NM_006031.5 L1243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr21:47754462 A>G maps to NM_006031.5 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr21:47769703 C>T maps to NM_006031.5 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr21:47851876 C>G maps to NM_006031.5 L2833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr21:47836563 G>A maps to NM_006031.5 V2244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr21:47746424 C>T maps to NM_006031.5 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr21:47841933 G>T maps to NM_006031.5 E2359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr14:71374686 C>T maps to NM_014982.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr14:71443717 C>T maps to NM_014982.2 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr14:71540496 C>G maps to NM_014982.2 L1696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr14:71443816 C>T maps to NM_014982.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr14:71524277 C>T maps to NM_014982.2 S1563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr14:71374674 C>G maps to NM_014982.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr14:71445357 C>T maps to NM_014982.2 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:233394743 G>C maps to NM_014801.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:233314876 G>A maps to NM_014801.3 F1037F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:233120094 G>T maps to NM_014801.3 G2123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:233190142 C>A maps to NM_014801.3 G1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:233394332 C>T maps to NM_014801.3 Q425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr11:65384335 C>T maps to NM_032223.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr11:65396145 C>T maps to NM_032223.2 H1261H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr11:65404048 C>T maps to NM_032223.2 L1927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:65401670 G>A maps to NM_032223.2 L1515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr11:65398044 C>T maps to NM_032223.2 L1480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr11:65403731 C>T maps to NM_032223.2 L1849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr11:65392688 T>C maps to NM_032223.2 C989C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr11:65386062 G>C maps to NM_032223.2 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:65397009 C>T maps to NM_032223.2 L1340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr11:65385687 G>A maps to NM_032223.2 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr11:65392932 C>T maps to NM_032223.2 A1029A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr7:100205570 C>T maps to NM_002593.3 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:100201772 G>A maps to NM_002593.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr3:142542440 C>A maps to NM_013363.3 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:7697403 C>G did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr5:95743997 C>G maps to NM_000439.4 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr5:95761559 G>T maps to NM_000439.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr5:95761556 G>A maps to NM_000439.4 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr20:17446012 C>G maps to NM_002594.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr20:17339072 G>A maps to NM_002594.2 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr20:17462486 C>T maps to NM_002594.2 D563D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:1482189 G>T maps to NM_017573.3 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr19:1487785 G>A maps to NM_017573.3 N197N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr19:1487827 G>A maps to NM_017573.3 Y183Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:1481868 G>A maps to NM_017573.3 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr9:78682876 G>A maps to NM_001190482.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr9:78784731 C>T maps to NM_001190482.1 Q578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr9:78506219 C>G maps to NM_001190482.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr9:78789980 G>A maps to NM_001190482.1 V612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr15:101938608 C>T maps to NM_002570.3 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:101872077 C>A maps to NM_002570.3 E672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr15:101929697 C>A maps to NM_002570.3 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr15:101938722 G>A maps to NM_002570.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:117089802 G>C maps to NM_004716.2 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:117090348 C>T maps to NM_004716.2 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr11:117079767 G>A maps to NM_004716.2 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:55523772 G>A maps to NM_174936.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:55523841 C>G maps to NM_174936.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:53844766 C>T maps to NM_021213.3 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr2:70502123 C>T maps to NM_016297.3 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:70485406 C>T maps to NM_016297.3 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr2:70502234 C>G maps to NM_016297.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr2:70502264 C>G maps to NM_016297.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:148743623 G>C maps to NM_024028.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr5:148743656 C>T maps to NM_024028.3 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr3:195975135 G>A maps to NM_005017.2 H92H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr3:195965720 G>A maps to NM_005017.2 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr23:24605406 C>G did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr23:24625955 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr23:24608262 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:79864645 G>A maps to NM_001184917.1 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:99002547 C>T maps to NM_014891.6 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr7:98998029 A>G maps to NM_014891.6 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:242793368 C>T maps to NM_005018.2 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr2:242793385 G>A maps to NM_005018.2 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:167414890 G>A maps to NM_145859.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:105179395 G>A maps to NM_014976.1 V736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr10:105198493 C>T maps to NM_014976.1 I1318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr10:105179398 G>A maps to NM_014976.1 K737K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr10:105203080 G>A maps to NM_014976.1 E1705E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr10:105184742 G>A maps to NM_014976.1 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr10:105164885 G>A maps to NM_014976.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:34912526 C>T maps to NM_032346.1 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:34912555 C>T maps to NM_032346.1 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr19:34895678 C>T maps to NM_032346.1 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:34900376 G>A maps to NM_032346.1 Q216Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr19:34912447 C>G maps to NM_032346.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr10:112650397 G>C maps to NM_014456.4 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr10:112653877 C>T maps to NM_014456.4 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:33072193 G>A maps to NM_004708.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:33877664 C>T maps to NM_001162429.1 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr3:33870427 G>A maps to NM_001162429.1 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:33886998 C>T maps to NM_001162429.1 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr3:33906751 C>T maps to NM_001162429.1 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr9:125588972 G>A maps to NM_005388.4 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr9:125585293 C>A did not map to a codon.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr9:125582590 G>A maps to NM_005388.4 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr9:125582723 G>A maps to NM_005388.4 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr9:125588972 G>A maps to NM_005388.4 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr4:56448308 A>T maps to NM_152401.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:101188177 G>A maps to NM_024065.4 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:771390 G>A maps to NM_182612.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr6:165749622 C>T maps to NM_001130690.1 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr6:165752790 C>T maps to NM_001130690.1 K718K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:165756991 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr2:178528628 C>A maps to NM_016953.3 E871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:178705091 C>T maps to NM_016953.3 E462E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:178936648 G>T maps to NM_016953.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr2:178936252 C>T maps to NM_016953.3 Q304Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr2:178682620 C>T maps to NM_016953.3 G536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr2:178769907 G>A maps to NM_016953.3 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr3:57543221 G>A maps to NM_177966.5 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr3:57543209 C>T maps to NM_177966.5 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr2:183129136 T>A maps to NM_005019.3 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr2:183387049 A>G maps to NM_005019.3 Y18Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:54964089 G>A maps to NM_000924.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr12:54967205 C>T maps to NM_000924.3 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr12:54969788 C>T maps to NM_000924.3 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr12:54970358 C>T maps to NM_000924.3 Q461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr12:54969375 C>G maps to NM_000924.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:31904656 C>A maps to NM_001191057.1 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:72292402 G>A maps to NM_002599.3 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr11:72297214 C>A maps to NM_002599.3 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr11:72293529 G>A maps to NM_002599.3 F603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr12:20786632 C>A maps to NM_000921.3 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr12:20523042 G>A maps to NM_000921.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:20523042 G>A maps to NM_000921.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:20523042 G>A maps to NM_000921.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr12:20774240 G>A maps to NM_000921.3 W479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr12:20833108 G>A maps to NM_000921.3 S1110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr12:20523042 G>A maps to NM_000921.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr12:20522886 C>T maps to NM_000921.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:20523042 G>A maps to NM_000921.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:20801785 G>A maps to NM_000921.3 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr12:20833190 A>T maps to NM_000921.3 K1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr12:20799862 G>C maps to NM_000921.3 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:20522856 C>T maps to NM_000921.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr12:20790053 C>A maps to NM_000921.3 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:14825540 G>A maps to NM_000922.3 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:14666331 C>T maps to NM_000922.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:14665989 C>T maps to NM_000922.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr11:14839735 G>A maps to NM_000922.3 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr11:14852316 G>A maps to NM_000922.3 K627K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:10571771 C>T maps to NM_001111307.1 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:10577957 G>T maps to NM_001111307.1 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr19:10572256 G>C maps to NM_001111307.1 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr19:10561325 C>G maps to NM_001111307.1 S223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:10561308 C>T maps to NM_001111307.1 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr19:10568571 G>T maps to NM_001111307.1 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr1:66798287 G>A maps to NM_001037341.1 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:66838228 G>A maps to NM_001037341.1 E693E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:66798095 C>T maps to NM_001037339.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:66833732 T>C maps to NM_001037341.1 Y549Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:66723490 C>T maps to NM_001037341.1 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:66798110 C>T maps to NM_001037339.1 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr19:18333083 G>A maps to NM_000923.3 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr19:18327577 C>G maps to NM_000923.3 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:18321949 G>C maps to NM_000923.3 S643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:18327583 C>T maps to NM_000923.3 Q484Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr19:18322676 C>T maps to NM_000923.3 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:144930641 G>C maps to NM_001002811.1 S356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:145075663 C>A maps to NM_022359.5 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr1:144922569 T>C maps to NM_014644.4 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:144952286 C>T maps to NM_014644.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:144918838 C>T maps to NM_014644.4 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:144859923 G>A maps to NM_014644.4 L2054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:144876028 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr1:145075750 G>A maps to NM_022359.5 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:144879301 G>C maps to NM_014644.4 S1383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:144859896 G>A maps to NM_014644.4 Q2063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr1:144882628 C>T maps to NM_014644.4 G1130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:144917917 G>A maps to NM_014644.4 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:144931521 G>A maps to NM_001002811.1 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr1:144879255 C>A maps to NM_014644.4 L1398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr1:144882723 G>A maps to NM_014644.4 Q1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr1:144857642 G>C maps to NM_014644.4 G2137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr1:144873973 G>A maps to NM_014644.4 T1661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:144857624 G>A maps to NM_014644.4 I2143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:144882661 G>C maps to NM_014644.4 L1119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:144864172 G>A maps to NM_014644.4 F1974F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:144877096 G>A maps to NM_014644.4 F1530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr1:144864198 C>A maps to NM_014644.4 E1966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr1:144854587 C>T maps to NM_014644.4 Q2294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr1:145075754 C>T maps to NM_022359.5 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr1:144994686 C>G maps to NM_014644.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr1:144859921 C>T maps to NM_014644.4 L2054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr1:144994656 G>T maps to NM_014644.4 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:144881465 G>A maps to NM_014644.4 Q1244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:145075741 G>A maps to NM_022359.5 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:144865845 G>A maps to NM_014644.4 R1912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr1:144879301 G>C maps to NM_014644.4 S1383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr1:144916617 G>A maps to NM_014644.4 I579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr1:144912276 C>T maps to NM_014644.4 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:144931237 T>A maps to NM_001002811.1 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr1:144917522 G>A maps to NM_014644.4 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr1:144931144 T>A maps to NM_001002811.1 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:144863442 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:145015894 G>A maps to NM_001198832.1 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr1:144930940 C>T maps to NM_001002811.1 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:144882664 G>A maps to NM_014644.4 L1118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr1:144917522 G>A maps to NM_014644.4 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:144865879 G>C maps to NM_014644.4 L1900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr4:120432219 C>G maps to NM_001083.3 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr4:120463679 C>T maps to NM_001083.3 G502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr4:120528155 G>C maps to NM_001083.3 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr4:120528238 C>T maps to NM_001083.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr4:654368 G>T maps to NM_000283.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47W-01A-11D-A23U-08 chr4:650709 C>A maps to NM_000283.3 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr4:628476 C>T maps to NM_000283.3 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr4:629721 G>C maps to NM_000283.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:95400232 G>C maps to NM_006204.3 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr10:95422891 C>T maps to NM_006204.3 V825V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr10:95418766 T>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr17:79618681 C>G maps to ENST00000331056 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:66631544 G>A maps to ENST00000401827 Q477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr8:66753680 G>A maps to ENST00000401827 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:136472383 C>T maps to NM_018945.3 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr6:136476806 C>T maps to NM_018945.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:85634392 C>A maps to NM_002605.2 S278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr15:85669487 G>A maps to NM_002605.2 E712E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:76645302 A>G maps to NM_003719.3 K312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr5:76722315 C>T maps to NM_003719.3 Y865Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:44188329 C>A maps to NM_002606.2 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr21:44190895 C>T maps to NM_002606.2 D558D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr21:44174149 C>T maps to NM_002606.2 D262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr22:39626221 G>A maps to NM_002608.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:39639935 G>A maps to NM_002608.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr22:39636868 G>A maps to NM_033016.2 I3I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr22:39636859 G>A maps to NM_033016.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr4:157732169 C>T did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr4:157684304 G>C maps to NM_016205.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr4:157892046 G>A maps to NM_016205.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr4:157891977 C>T maps to NM_016205.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:104034598 C>T maps to NM_025208.4 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr4:55127288 C>G maps to NM_006206.4 S26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr4:55155223 C>G maps to ENST00000507166 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr4:55127277 C>T maps to NM_006206.4 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:55155178 C>T maps to ENST00000507166 Y686Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr4:55141140 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr4:55129981 C>T maps to NM_006206.4 Y172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T4-01A-11D-A391-08 chr4:55124985 T>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr4:55140749 T>C maps to NM_006206.4 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr4:55144102 A>G maps to ENST00000507166 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr4:55141104 C>G maps to ENST00000507166 S344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:149498308 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr5:149514571 G>C maps to NM_002609.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr5:149497413 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr8:17486203 C>G maps to NM_006207.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr23:19377093 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:19369481 C>T did not map to a codon.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr23:19369503 G>A did not map to a codon.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr23:19375800 G>C did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr23:19375796 T>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:19373562 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr23:19371235 C>T did not map to a codon.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr4:96761852 C>T maps to NM_005390.4 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr4:96761706 C>T maps to NM_005390.4 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr16:335328 C>T maps to NM_006849.2 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr15:44038745 C>T maps to NM_005313.4 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr7:148703135 G>A maps to NM_004911.4 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:122811200 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:122811200 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:122829804 C>G maps to NM_006810.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr2:10929919 G>C maps to ENST00000381611 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr16:20410610 G>A maps to NM_174924.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr16:20380852 G>A maps to NM_174924.1 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr16:20384168 G>A maps to NM_174924.1 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr16:20410433 G>A maps to NM_174924.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr2:173429254 C>T maps to ENST00000392571 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr23:24512955 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:24483595 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:24512898 A>G did not map to a codon.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr23:24483620 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr8:22442666 C>T maps to NM_021630.5 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr8:22452128 G>A maps to NM_176871.3 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr8:22438122 G>A maps to NM_021630.5 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:131607547 G>A maps to NM_003687.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr5:131607482 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr4:95561489 C>G maps to NM_006457.3 S391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr4:95583675 C>T maps to NM_006457.3 C563C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr4:95506868 G>A maps to NM_006457.3 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr4:95376510 C>T maps to NM_006457.3 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:176910876 G>A maps to NM_005451.3 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr8:94935517 A>T maps to NM_001161778.1 K470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr8:94935153 T>C maps to NM_001161778.1 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:66919263 G>A maps to NM_020786.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr16:66919440 G>A maps to NM_020786.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr16:66919542 G>A maps to NM_020786.2 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:70164431 C>G maps to NM_017990.3 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr16:70161219 G>A maps to NM_017990.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr16:70190727 C>T maps to NM_017990.3 F862F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:70172861 G>C maps to NM_017990.3 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr16:70190471 C>G maps to NM_017990.3 S777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr20:30538145 C>T maps to NM_030815.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr20:30538145 C>T maps to NM_030815.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr20:30538124 G>A maps to NM_030815.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr4:39905709 C>T maps to NM_001100399.1 W445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:39978092 C>T maps to NM_001100399.1 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr4:39868596 C>T maps to NM_001100399.1 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:33327663 A>G maps to ENST00000400481 A977A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr13:33273918 G>A maps to ENST00000400481 Q551Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr13:33320234 C>A maps to ENST00000400481 I911I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr10:26998638 C>T maps to NM_014317.3 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:107780312 G>A maps to NM_020381.3 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr16:15098115 G>A maps to NM_015027.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr16:15110019 G>C maps to NM_015027.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr16:15129996 C>T maps to NM_015027.2 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr16:15125754 G>A maps to NM_015027.2 G521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr21:45170386 G>A maps to NM_003681.4 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr21:45170411 G>T maps to NM_003681.4 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr21:45173596 C>T maps to NM_003681.4 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr21:45170414 G>T maps to NM_003681.4 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr21:45161559 G>A maps to NM_003681.4 W52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr22:38061587 G>T maps to ENST00000442465 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:69508313 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr5:32048766 C>T maps to NM_178140.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:32093125 C>G maps to NM_178140.2 S2614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:32108239 G>T maps to NM_178140.2 *2840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr5:32090975 C>T maps to NM_178140.2 P2474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr5:32048733 C>T maps to NM_178140.2 R537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr5:32089374 G>T maps to NM_178140.2 E1941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr5:32048696 G>A maps to NM_178140.2 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:32087405 C>T maps to NM_178140.2 L1284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr5:31983536 G>A maps to NM_178140.2 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr5:32093068 C>A maps to NM_178140.2 S2595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr5:32090186 T>C maps to NM_178140.2 H2211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr11:119058154 C>T maps to ENST00000392817 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr23:153069337 C>G did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:153070101 G>A did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr23:153069708 G>A did not map to a codon.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr23:153072222 C>G did not map to a codon.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr23:153068840 G>C did not map to a codon.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr23:153070294 C>A did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr23:153073867 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr23:153069222 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr10:102789912 G>A maps to NM_001195263.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr10:119044971 G>A maps to NM_173791.3 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr10:119043390 G>C maps to NM_173791.3 V951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr10:119134252 G>A maps to NM_173791.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:21995704 C>T maps to ENST00000424898 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr3:73433184 G>A maps to NM_015009.1 D844D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr3:73432827 C>T maps to NM_015009.1 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr12:41966398 C>G maps to NM_001164595.1 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:41967406 C>T maps to NM_001164595.1 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr12:41967535 C>T maps to NM_001164595.1 I985I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr12:41585312 G>A maps to NM_001164595.1 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr12:118582394 C>G maps to NM_002567.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr6:4117577 C>T maps to NM_206836.2 W331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr6:4131045 G>A maps to NM_206836.2 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:4126370 C>T maps to NM_206836.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:57328267 G>A maps to NM_006210.2 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:57327166 A>G maps to NM_006210.2 P881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr19:57326046 G>A maps to NM_006210.2 Q1255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr19:57325245 C>A maps to NM_006210.2 E1522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr2:64323421 G>C maps to NM_020651.3 S176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr14:56757152 G>A maps to NM_021255.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr14:56755261 C>T maps to NM_021255.2 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr11:66241240 C>T maps to NM_145065.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:52096665 C>T maps to NM_015946.4 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr5:52096665 C>T maps to NM_015946.4 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr5:52096866 G>A maps to NM_015946.4 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr5:52096756 C>T maps to NM_015946.4 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:4577934 C>T maps to ENST00000301396 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:17480266 G>A maps to NM_148172.1 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr8:57354058 G>A maps to NM_001135690.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr17:8048195 C>G maps to NM_002616.2 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr17:8044596 G>C maps to NM_002616.2 S1221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:239184477 C>T maps to NM_022817.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr2:239185788 T>C maps to NM_022817.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr2:239185834 C>T did not map to a codon.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr2:239184399 G>A maps to NM_022817.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr2:239161852 G>C maps to NM_022817.2 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr2:239157732 C>T maps to NM_022817.2 T1196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:7887271 G>A maps to ENST00000377532 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr6:138417521 C>G maps to NM_022121.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr4:152682083 G>A maps to NM_004564.2 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:152680007 G>C maps to NM_004564.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr4:152682083 G>A maps to NM_004564.2 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:92147126 C>T maps to NM_000466.2 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr7:92120714 G>A maps to NM_000466.2 G1103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:145522726 C>G maps to NM_003846.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:33902992 G>C maps to NM_000286.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr17:33904531 G>A maps to NM_000286.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr17:33903109 G>A maps to NM_000286.2 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:61272940 G>T maps to NM_002618.3 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr2:61258968 C>T maps to NM_002618.3 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:10689947 G>A maps to NM_004565.2 Q346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:18566265 C>T maps to NM_017929.5 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:18566436 G>A maps to NM_017929.5 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr22:18561372 G>C maps to ENST00000399743 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr6:143810345 C>T maps to NM_003630.2 Q369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr12:7354880 G>T maps to NM_001131023.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr12:7354881 G>T maps to NM_001131023.1 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:179597762 C>T maps to NM_016559.1 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:179533668 G>A maps to NM_016559.1 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr6:42932116 G>A maps to NM_000287.3 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr6:42946261 C>G maps to NM_000287.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr6:42935165 G>C maps to NM_000287.3 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr17:8168265 G>A maps to NM_012393.2 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr17:8168742 C>T maps to NM_012393.2 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:8157481 A>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:161087762 C>T maps to NM_012394.3 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:53689714 G>A maps to NM_002624.3 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr6:33257969 G>A maps to NM_001185181.1 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:54959876 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:54975560 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:54975593 T>C did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:54971911 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr23:54959843 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:207242831 C>T maps to NM_006212.2 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:207228121 T>C maps to NM_006212.2 N20N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr10:6261551 G>A maps to NM_004566.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:6263483 C>T maps to NM_004566.3 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr10:6268180 C>T maps to NM_004566.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr10:6274865 A>G maps to NM_004566.3 K508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr10:6258136 G>T maps to NM_004566.3 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr3:48576046 C>T maps to NM_004567.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr3:48573772 G>T maps to NM_004567.2 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr3:48573802 G>C maps to NM_004567.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr21:45746743 G>A maps to NM_002626.4 *781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr21:45726579 C>G maps to NM_002626.4 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr21:45743761 C>T maps to NM_002626.4 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:3174630 C>T maps to NM_002627.3 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr10:3175394 A>G maps to NM_002627.3 R637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr10:3162098 C>T maps to NM_002627.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr10:3172045 C>T maps to NM_002627.3 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr10:3155562 G>A did not map to a codon.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr10:3150903 G>A maps to NM_002627.3 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr10:3161036 G>A maps to NM_002627.3 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:176827415 C>T maps to NM_001029886.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:24345318 C>G maps to NM_199346.1 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:61017152 C>T maps to ENST00000422676 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr7:44104936 G>A maps to NM_000290.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr23:77224589 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr23:77224406 T>C did not map to a codon.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr23:77224417 A>G did not map to a codon.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr23:77224938 G>A did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr23:77224637 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:77224500 G>T did not map to a codon.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr12:133294646 G>A maps to NM_001170543.1 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:133294682 C>T maps to NM_001170543.1 N232N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:133291560 C>T maps to NM_001170543.1 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr2:197763064 G>C maps to NM_024989.3 S279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr2:197777696 C>T maps to NM_024989.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr10:50724608 C>T maps to ENST00000515869 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr10:50723837 C>T maps to ENST00000515869 L909L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr1:230461090 C>T maps to ENST00000321327 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr1:230472983 C>T maps to ENST00000321327 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr6:41708251 G>C maps to NM_002630.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr6:41712174 G>A maps to NM_002630.3 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:98155284 C>T maps to ENST00000325141 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:10479589 C>T maps to NM_002631.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr23:77372876 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr23:77378443 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr23:77373555 T>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr23:77373556 A>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:49753658 G>A maps to NM_138733.4 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:49754285 C>T maps to NM_138733.4 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr19:17628173 C>G maps to NM_012088.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:17631814 G>A maps to NM_012088.2 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr19:46522874 G>A maps to NM_005091.2 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:46522603 C>T maps to NM_005091.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr19:15587201 C>G maps to NM_052890.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr19:15587363 C>T maps to NM_052890.3 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:15587402 G>C maps to NM_052890.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:153277444 G>T maps to NM_052891.1 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr1:153271631 G>A maps to NM_052891.1 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr1:153309654 A>G did not map to a codon.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:153317829 G>C maps to NM_020393.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr1:64095754 C>T maps to NM_002633.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:64114203 T>G maps to NM_002633.2 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:64059287 C>T maps to NM_002633.2 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:64125288 G>A maps to NM_002633.2 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr4:37850206 G>A maps to NM_018290.3 E449E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr4:37863157 G>A maps to NM_018290.3 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr4:37831698 T>A maps to NM_018290.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr4:37839180 C>T maps to NM_018290.3 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr11:74056621 C>T maps to NM_173582.3 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:74058369 C>T maps to NM_173582.3 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr6:83898499 T>C maps to ENST00000416472 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:70999455 C>T maps to NM_021965.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr9:71098903 G>T maps to NM_021965.3 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr9:71080072 C>T maps to NM_021965.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr9:70993113 G>T did not map to a codon.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr9:71002415 C>T maps to NM_021965.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:2263944 G>A maps to NM_001042371.2 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr19:18451502 G>A maps to NM_017712.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr19:18474199 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr15:99512766 G>A maps to NM_001102612.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:100996849 G>A maps to NM_000926.4 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr11:100998778 C>T maps to NM_000926.4 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr23:118374363 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr23:118374411 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:118370403 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr17:76395537 C>G maps to NM_024419.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr6:13182824 C>T maps to NM_030948.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr6:13206113 A>G maps to NM_030948.1 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr6:13206062 G>A maps to NM_030948.1 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:13182749 G>A did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr6:13160496 G>A maps to NM_030948.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr6:144098520 G>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr20:58318240 C>T maps to NM_080672.3 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr20:58416514 C>T maps to NM_080672.3 Y504Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:58349366 C>T maps to NM_080672.3 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr20:58381186 C>T maps to NM_080672.3 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr1:28800146 C>G maps to NM_023923.3 S312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr1:28819541 G>T maps to NM_023923.3 E688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:28785755 A>G maps to NM_023923.3 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr1:28817514 C>G maps to NM_023923.3 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr5:125952985 C>G maps to NM_032177.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:47486812 T>C maps to NM_002634.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:47486460 G>A maps to NM_002634.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr17:47482503 C>T maps to NM_002634.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr12:7077579 C>T maps to NM_001144831.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr12:9087790 G>A maps to ENST00000433083 E870E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr3:169896668 C>T maps to NM_024947.3 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr23:22056608 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr23:22051147 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr23:22196453 C>G did not map to a codon.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr23:22094532 G>C did not map to a codon.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr23:22112194 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:22095671 C>G did not map to a codon.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr6:33381072 G>A maps to NM_024165.2 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:33380559 G>A maps to NM_024165.2 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:33383646 G>C maps to NM_024165.2 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:33383742 G>A maps to NM_024165.2 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr6:33383613 C>T maps to NM_024165.2 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:33381289 G>A maps to NM_024165.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr6:170112609 G>A maps to NM_018288.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr6:170118986 C>T maps to NM_018288.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr13:50092215 G>A maps to NM_001040443.1 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr17:27244464 C>T maps to NM_001033561.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr17:27254013 G>T maps to NM_001033561.1 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr17:27233883 C>T maps to NM_001033561.1 Q890Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr17:27248812 C>T maps to NM_001033561.1 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr17:27251023 C>T maps to NM_001033561.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr17:27237352 G>A maps to NM_001033561.1 I750I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr17:27235834 C>T maps to NM_001033561.1 V808V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr1:6681669 G>A maps to NM_153812.2 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr7:11101607 G>A maps to ENST00000303905 E850E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr7:11053503 T>C maps to ENST00000303905 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr5:133914400 C>T maps to ENST00000448712 D649D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr5:133914844 G>A maps to ENST00000448712 E797E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr5:133902050 C>T maps to ENST00000448712 Y421Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr5:133896637 T>C maps to ENST00000448712 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr23:46884243 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:46913946 G>A did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr23:46913958 G>C did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr23:46913970 G>T did not map to a codon.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr23:46898445 G>T did not map to a codon.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr4:129778585 G>T maps to NM_199320.2 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr9:123620305 C>T maps to NM_015651.1 E553E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:96415472 C>T maps to NM_005392.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr9:96398771 C>G maps to NM_005392.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:34459578 G>A maps to NM_016436.4 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr20:34457363 G>T maps to NM_016436.4 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:34451264 G>T maps to NM_016436.4 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr20:34389476 C>T maps to NM_016436.4 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr20:34526617 G>T did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr20:34459027 G>C maps to NM_016436.4 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr8:133844493 G>T maps to ENST00000395386 E588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr8:133811031 C>T maps to ENST00000395386 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr8:133826911 A>T maps to ENST00000395386 K322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:46100683 C>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr22:45312306 G>A maps to NM_138415.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr6:64421840 C>T maps to NM_015153.2 Q1453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:64389976 G>C maps to NM_015153.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr6:64394071 C>G maps to NM_015153.2 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr6:64395369 C>T maps to NM_015153.2 Q583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr6:64413515 C>T maps to NM_015153.2 Q1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr6:64404645 C>G maps to NM_015153.2 S891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr6:64422760 A>C maps to NM_015153.2 A1759A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr6:64356519 C>T maps to NM_015153.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr23:133559261 G>C did not map to a codon.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr23:133512097 G>T did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr23:133549105 G>C did not map to a codon.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr23:133559265 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr23:133511785 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr23:133511768 C>G did not map to a codon.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr23:133527537 C>T did not map to a codon.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr23:54069200 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr23:54069087 A>T did not map to a codon.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr23:54012299 T>C did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:54037672 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr23:54022188 G>A did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr23:54048788 G>A did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr23:53989323 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:54037668 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:54019225 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:54014217 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr1:120286647 C>T maps to NM_006623.3 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr1:120254677 C>T maps to NM_006623.3 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr6:79711643 G>A maps to NM_017934.5 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:79711636 G>A maps to NM_017934.5 Q620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr23:71839144 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:71846899 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr23:71843048 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:71915559 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:71802424 G>T did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:71839102 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr23:71840610 A>C did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:71876046 C>T did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:71800852 C>T did not map to a codon.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr23:71802307 T>C did not map to a codon.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr23:71825147 C>A did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:71904406 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr23:71895935 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:71800982 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr23:71843000 C>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:71932684 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr23:71887292 G>C did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:18926149 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:18913259 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:18959732 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr23:18936903 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr23:18923971 C>G did not map to a codon.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr23:18936889 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:18911739 C>G did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:19002044 C>G did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr23:18919673 C>A did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:18918792 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:18943856 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr16:47549429 A>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:47683099 G>A maps to NM_000293.2 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr16:47694614 C>G maps to NM_000293.2 S694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr16:47684516 C>G maps to NM_000293.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr7:56151373 C>A maps to NM_006213.3 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr16:30767795 C>T maps to NM_000294.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:201437830 C>T maps to NM_012396.3 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr1:201437598 T>A maps to NM_012396.3 K106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr1:201437605 G>A maps to NM_012396.3 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr1:201437605 G>T maps to NM_012396.3 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr11:118485344 C>T maps to NM_015157.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:118498654 C>G maps to NM_015157.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr11:118486901 C>A maps to NM_015157.2 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr3:111658335 G>A maps to NM_001134438.1 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:111603862 C>T maps to NM_001134438.1 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr3:111688639 C>G maps to NM_001134438.1 S1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:111603733 C>G maps to NM_001134438.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr3:111602963 C>T maps to NM_001134438.1 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:111632188 C>A maps to NM_001134438.1 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr3:111604250 G>T maps to NM_001134438.1 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:111603688 A>G maps to NM_001134438.1 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr18:60612350 G>A maps to NM_194449.2 A1057A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr18:60646310 G>T maps to NM_194449.2 E1601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr18:60625989 G>A maps to NM_194449.2 L1151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr16:71701148 G>C maps to NM_015020.2 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:71718465 G>A maps to NM_015020.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr16:71683848 C>A maps to NM_015020.2 P972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr16:71706187 C>A maps to NM_015020.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr16:71710365 G>C maps to NM_015020.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr16:71682798 T>A maps to NM_015020.2 A1322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr17:47302318 G>A maps to NM_001143804.1 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr17:47302264 G>T maps to NM_001143804.1 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr11:71950870 G>A maps to NM_005169.3 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr4:41747865 G>T maps to NM_003924.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr4:41749395 C>T maps to NM_003924.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr11:609397 G>A maps to ENST00000264555 L1314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:607921 G>A maps to ENST00000264555 T822T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:607588 C>A maps to ENST00000264555 I711I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr11:596979 C>T maps to ENST00000264555 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:608500 A>G maps to ENST00000264555 G1015G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr1:114243457 G>A maps to NM_006608.2 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:114246789 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:77539722 C>G maps to ENST00000427986 S258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr7:77539722 C>G maps to ENST00000427986 S258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr7:77569960 C>T maps to ENST00000427986 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr7:77549628 A>T maps to ENST00000427986 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:13330473 G>A maps to NM_006214.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr9:131704016 C>T maps to NM_174933.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:75737666 C>T maps to NM_015886.3 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr8:75756241 G>A maps to NM_015886.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr6:36930927 G>T maps to NM_153370.2 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr6:36930789 A>T maps to NM_153370.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr6:36926997 G>A maps to NM_153370.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr6:36931308 C>T maps to NM_153370.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:43804727 G>A maps to NM_002638.3 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:99416091 G>A maps to ENST00000416867 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr10:99416705 G>T maps to ENST00000416867 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr10:99426241 C>T maps to ENST00000416867 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr10:99416116 C>T maps to ENST00000416867 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:25253957 C>A maps to NM_018323.3 S95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr4:25254051 C>T maps to NM_018323.3 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:21083622 G>A maps to NM_058004.2 L1496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr22:21174066 G>T maps to NM_058004.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr22:21107282 C>T maps to NM_058004.2 E907E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr22:21062352 C>T maps to NM_058004.2 Q2039Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr22:21161725 G>C maps to NM_058004.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:151288550 G>C maps to NM_002651.2 S148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr1:151288429 C>A maps to NM_002651.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:151288628 G>C maps to NM_002651.2 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr15:68466150 C>T maps to NM_016166.1 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr1:145580262 C>T maps to NM_006099.3 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr1:145578391 C>T maps to NM_006099.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr19:4037635 C>G maps to NM_015897.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr19:4013123 G>A maps to NM_015897.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr13:73573051 G>C maps to NM_006346.2 V714V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr11:85733471 A>T maps to ENST00000393343 Y130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr22:38470961 C>G maps to NM_012407.3 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr22:38465037 A>G did not map to a codon.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr22:38469020 G>C maps to NM_012407.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr15:65114471 G>A maps to ENST00000333425 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr15:65113660 G>A maps to ENST00000333425 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr23:15349791 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr23:15344034 C>G did not map to a codon.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr23:15344105 T>C did not map to a codon.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr23:15343167 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:55611486 G>A maps to ENST00000164305 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr1:172410940 A>G maps to NM_153747.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:46815244 C>G maps to NM_173074.2 *207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr4:517588 G>A maps to NM_001127178.1 W652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr4:517378 G>A maps to NM_001127178.1 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr4:515726 G>A maps to NM_001127178.1 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr4:520827 C>T maps to NM_001127178.1 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr4:524278 G>A maps to NM_001127178.1 T772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr1:160000590 G>A maps to NM_145167.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:160001329 G>T maps to NM_145167.2 S67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:35095511 G>A maps to NM_032634.2 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr9:35092404 C>T maps to NM_032634.2 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr9:35094273 G>T maps to NM_032634.2 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr9:35094309 G>A maps to NM_032634.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr9:35091999 C>T maps to NM_032634.2 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr9:35091877 C>T maps to NM_032634.2 W669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr21:38444857 C>T maps to NM_153681.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr16:633558 C>T maps to NM_148920.1 P736P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr16:624460 C>T maps to NM_148920.1 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr16:633033 G>A maps to NM_148920.1 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:632998 C>T maps to NM_148920.1 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:207105028 G>A maps to NM_002644.3 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:207112587 C>T maps to NM_002644.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr1:207104856 G>C maps to NM_002644.3 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:207110449 G>A maps to NM_002644.3 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr20:44048163 G>A maps to NM_015937.4 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr20:44048151 C>G maps to NM_015937.4 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr20:44053207 C>T maps to NM_015937.4 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr20:33162907 C>T maps to NM_080476.4 Q398Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr20:33163012 G>A maps to NM_080476.4 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr20:33225729 G>A maps to NM_080476.4 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr20:33148711 C>T maps to NM_080476.4 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:27121286 C>T maps to NM_017837.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:27124266 C>T maps to NM_017837.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:27120689 C>T maps to NM_017837.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:27124127 G>A maps to NM_017837.2 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr17:34893432 C>G maps to NM_178517.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr17:34893189 C>A maps to NM_178517.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr17:34894045 C>T maps to NM_178517.3 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:34893289 G>T maps to NM_178517.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:89442802 G>C maps to NM_001042616.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr3:196675226 C>A maps to NM_025163.2 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:196674501 G>A maps to NM_025163.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr19:49952743 C>A maps to NM_017916.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr11:111941993 G>A maps to NM_138789.3 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr11:111941230 G>A maps to NM_138789.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr10:98416659 C>T maps to NM_152309.2 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr10:98380258 A>G maps to NM_152309.2 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr11:17156368 G>C maps to NM_002645.2 S702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:17124284 G>A maps to NM_002645.2 R1259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr11:17169138 G>A maps to NM_002645.2 N495N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:17112889 G>A maps to NM_002645.2 F1623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr11:17113137 G>A maps to NM_002645.2 R1570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr11:17172071 G>A maps to NM_002645.2 Q434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr11:17132021 C>T maps to NM_002645.2 L1167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:204416580 C>T maps to NM_002646.3 Q824Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:204412706 G>A maps to NM_002646.3 L962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:204438083 G>A maps to NM_002646.3 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:204401356 C>A maps to NM_002646.3 E1376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:204402480 G>A maps to NM_002646.3 Q1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:204403031 G>A maps to NM_002646.3 I1244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:204423822 G>A maps to NM_002646.3 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:204412718 C>T maps to NM_002646.3 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:204412718 C>T maps to NM_002646.3 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:204413284 C>T maps to NM_002646.3 L926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:204401445 G>C maps to NM_002646.3 S1346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr12:18747478 G>T maps to NM_004570.4 E1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:18435560 C>T maps to NM_004570.4 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr12:18534753 C>A maps to NM_004570.4 P604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr12:18435431 C>T maps to NM_004570.4 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr18:39637853 C>G maps to ENST00000398870 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr18:39644702 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr3:178948116 G>A maps to NM_006218.2 V963V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr3:178919315 G>C maps to NM_006218.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr3:178937837 A>G maps to NM_006218.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr3:178938788 T>C maps to NM_006218.2 N677N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr3:138478131 C>T maps to NM_006219.1 W18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr3:138403465 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr3:138474749 T>C maps to NM_006219.1 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr3:138409893 C>A maps to NM_006219.1 E662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:138376656 T>C maps to NM_006219.1 G939G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr1:9775627 G>T maps to ENST00000361110 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr7:106509784 T>C maps to NM_002649.2 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr7:106509635 C>T maps to NM_002649.2 R544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr7:106509094 C>G maps to NM_002649.2 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr7:106523484 C>T maps to NM_002649.2 I879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr7:106508329 G>A maps to NM_002649.2 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:67586646 G>T maps to NM_181504.2 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr5:67576354 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr5:67576547 C>G maps to ENST00000396611 S276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr5:67592070 C>T maps to ENST00000396611 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr19:18271738 C>T maps to NM_005027.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr19:18274188 G>A maps to NM_005027.2 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:46532609 C>A maps to NM_001114172.1 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:130405055 A>G maps to NM_014602.2 I1158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:130435419 G>C maps to NM_014602.2 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr3:130452779 A>G maps to NM_014602.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:130463768 T>A maps to NM_014602.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:8791858 G>A maps to NM_001142633.1 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:8814739 G>A maps to NM_001142633.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:8794165 C>G maps to NM_001142633.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:8808181 G>A maps to NM_001142633.1 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr17:8794165 C>T maps to NM_001142633.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:8725948 G>A maps to NM_001010855.2 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr17:8736296 G>C maps to NM_001010855.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:209203276 C>T maps to NM_015040.3 Q1553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr2:209189657 A>T maps to NM_015040.3 R785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:209188990 C>G maps to NM_015040.3 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr2:209195256 C>T maps to NM_015040.3 Q1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr2:209138366 C>T maps to NM_015040.3 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:209190133 C>T maps to NM_015040.3 Q867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr2:209189748 C>T maps to NM_015040.3 Q816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr2:209182625 C>G maps to NM_015040.3 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr7:99971726 C>G maps to NM_013439.2 S42*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-GV-A3JZ-01A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:99957060 C>T maps to ENST00000413850 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr7:99957140 G>A maps to ENST00000413850 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:48772313 G>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:48775886 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr22:50355454 C>T maps to NM_001001852.3 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr22:50356726 C>G maps to NM_001001852.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:71401592 A>G did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr1:20972085 G>A maps to NM_032409.2 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr7:77010666 A>G maps to NM_017439.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr7:77011906 C>T maps to NM_017439.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:76982907 G>T maps to NM_017439.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:76984618 G>A maps to NM_017439.3 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr7:77004395 G>C maps to NM_017439.3 S255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:76950708 A>G maps to NM_017439.3 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr7:76982336 G>T maps to NM_017439.3 S472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr7:142836241 C>T maps to NM_002652.2 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr10:22839617 G>A maps to NM_005028.4 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr10:22830754 G>C maps to NM_005028.4 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:36955629 G>C maps to NM_003559.4 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr12:57985170 C>T maps to NM_024779.4 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr12:57989741 G>C maps to NM_024779.4 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr12:57985143 C>T maps to NM_024779.4 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:151205034 C>T maps to NM_001135638.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:151205058 C>T maps to NM_001135638.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr1:151196877 C>G maps to NM_001135638.1 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr19:3661065 G>T maps to NM_012398.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr9:130691966 C>A maps to NM_001135219.1 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr9:130689457 G>A maps to NM_001135219.1 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr9:130688173 G>T maps to NM_001135219.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr17:27382166 G>C maps to NM_016518.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr17:27370278 G>A maps to NM_016518.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr17:27379940 G>A maps to NM_016518.2 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:15509314 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr23:15474082 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr23:15509376 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr17:10728776 G>A maps to NM_001101387.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr22:32017072 G>C maps to ENST00000422296 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr17:65574310 C>T maps to NM_012417.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr17:65688746 A>T maps to NM_012417.2 K248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr11:67265123 A>G maps to NM_004910.2 F603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr11:67265150 C>G did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr11:67265444 G>C maps to NM_004910.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr12:123471234 C>T maps to NM_020845.2 P1185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr12:123482008 C>T maps to NM_020845.2 K445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr12:123470828 G>A maps to NM_020845.2 R1265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr12:123481052 C>A maps to NM_020845.2 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr12:123494478 G>A maps to NM_020845.2 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:123494487 G>A maps to NM_020845.2 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr12:123472866 C>A maps to NM_020845.2 E971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:6374546 C>A maps to NM_031220.3 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:6376070 C>T maps to NM_031220.3 E445E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr17:6358828 C>T maps to NM_031220.3 R918R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr17:6387577 C>T maps to NM_031220.3 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr10:3191832 G>C maps to ENST00000380989 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr10:3180443 G>A maps to ENST00000380989 L1002L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr5:134364924 C>T maps to NM_002653.4 Q163Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:111539517 G>A maps to NM_153426.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr4:111539547 T>C maps to NM_153426.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr10:103990675 C>T maps to NM_005029.3 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr12:130832681 C>T maps to NM_004764.4 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:130830391 G>A maps to NM_004764.4 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:130831077 T>A maps to NM_004764.4 C160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr12:130830395 C>T maps to NM_004764.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:130851732 C>T maps to NM_004764.4 Q751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr12:130847596 C>T maps to NM_004764.4 R701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr22:25144924 G>A maps to NM_001008496.2 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr22:25119194 C>T maps to NM_001008496.2 K762K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr22:25150117 G>C maps to NM_001008496.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr11:94316736 T>C did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr11:94316612 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:94328538 C>G maps to NM_152431.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr11:94352997 A>T maps to NM_152431.2 V747V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr11:94353177 G>A maps to NM_152431.2 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr23:68382054 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr23:68382313 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr23:68382761 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr23:68381655 C>T did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:68382148 C>T did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr23:68382894 G>C did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr23:68383029 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:68381780 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr16:2153702 G>T maps to NM_001009944.2 G2785G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:2159440 G>A maps to NM_001009944.2 I1909I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr16:2155924 G>A maps to NM_001009944.2 Q2602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr16:2155952 G>A maps to NM_001009944.2 T2592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:2168841 G>A maps to NM_001009944.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr16:2140902 G>C maps to NM_001009944.2 L3995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:2167659 G>T maps to NM_001009944.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr16:2159521 C>A maps to NM_001009944.2 T1882T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:2159569 G>C maps to NM_001009944.2 L1866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr16:2161006 T>C maps to NM_001009944.2 P1387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:2155379 C>T maps to NM_001009944.2 L2653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr16:2150176 C>A maps to NM_001009944.2 V3234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:2152828 G>A maps to NM_001009944.2 F2978F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr7:47892788 C>T maps to NM_138295.3 V1632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr7:47876632 G>A maps to NM_138295.3 Y1943Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:47898447 G>A maps to NM_138295.3 Y1395Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr7:47955029 G>A maps to NM_138295.3 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr7:47884663 G>A maps to NM_138295.3 L1722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr7:47930252 T>C maps to NM_138295.3 Q854Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr7:47869715 G>C maps to NM_138295.3 G2160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr7:47906118 C>G maps to NM_138295.3 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr7:47879073 G>T maps to NM_138295.3 T1913T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr7:47925652 C>G did not map to a codon.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr7:47904828 C>T maps to NM_138295.3 V1378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr7:47897388 C>T maps to NM_138295.3 E1468E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr7:47832233 T>C maps to NM_138295.3 Q2839Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr7:47855055 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr7:47968938 G>A maps to NM_138295.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr7:47886601 T>C maps to NM_138295.3 L1676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr16:81249934 G>A maps to NM_052892.3 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:81198280 G>A maps to NM_052892.3 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:81164154 G>A maps to NM_052892.3 F1984F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr16:81173268 G>A maps to NM_052892.3 I1822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr4:88987030 G>A maps to NM_000297.2 R786R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr4:88996750 C>T maps to NM_000297.2 Q938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr4:88986958 C>T maps to NM_000297.2 Y762Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr4:88987021 G>A maps to NM_000297.2 E783E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr10:102051056 C>A did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr10:102056961 C>T maps to NM_016112.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr10:102049816 C>T maps to NM_016112.2 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr2:42284439 C>T maps to NM_138370.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:46654092 C>G maps to NM_006071.1 L1709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:46655580 A>G maps to NM_006071.1 H1213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr22:46654035 G>A maps to NM_006071.1 I1728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr22:46654758 G>A maps to NM_006071.1 Y1487Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr22:46654086 C>T maps to NM_006071.1 L1711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr22:46652705 G>A maps to NM_006071.1 L2172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr22:46656639 G>A maps to NM_006071.1 N860N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr22:46654032 G>C maps to NM_006071.1 V1729V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr6:51523770 G>C maps to NM_138694.3 S3718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr6:51771088 G>C maps to NM_138694.3 L2244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr6:51889372 G>A maps to NM_138694.3 F1745F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:51929768 G>A maps to NM_138694.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr6:51923137 T>G maps to NM_138694.3 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:51908450 G>A maps to NM_138694.3 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr6:51497480 C>T maps to NM_138694.3 L3849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr6:51497482 A>G maps to NM_138694.3 L3849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:51612669 G>A maps to NM_138694.3 F3248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr6:51720705 G>T maps to NM_138694.3 I2632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr6:51497405 C>T maps to NM_138694.3 L3874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr6:51824737 G>C maps to NM_138694.3 V1946V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr6:51613214 G>A maps to NM_138694.3 L3067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr6:51497362 T>A maps to NM_138694.3 K3889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr6:51768829 C>T maps to NM_138694.3 T2273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr6:51890269 G>A maps to NM_138694.3 S1446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr6:51524342 C>T maps to NM_138694.3 L3527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr6:51934256 G>C maps to NM_138694.3 S259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr6:51712575 G>A maps to NM_138694.3 L2702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr6:51890112 G>A maps to NM_138694.3 L1499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:51824752 T>C maps to NM_138694.3 Q1941Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr6:51720688 A>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:51776681 G>C maps to NM_138694.3 L2135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:51949709 G>A maps to NM_138694.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr8:110457503 G>A maps to ENST00000426474 V1802V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:110476717 C>T maps to ENST00000426474 L2553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr8:110489536 C>T maps to ENST00000426474 Q3001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr8:110535086 C>T maps to ENST00000426474 Q4101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr8:110448689 T>C did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:110510689 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:110394706 T>C maps to ENST00000426474 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr8:110412386 G>A maps to ENST00000426474 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr8:110424513 G>A maps to ENST00000426474 Q702Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr8:110489478 G>A maps to ENST00000426474 Q2981Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr8:110460480 T>C maps to ENST00000426474 D1962D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr8:110374844 C>T maps to ENST00000426474 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr8:110503227 C>T maps to ENST00000426474 R3338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr8:110495273 C>G maps to ENST00000426474 L3172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr8:110439237 C>T maps to ENST00000426474 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr8:110410760 C>G maps to ENST00000426474 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr8:110530433 G>T maps to ENST00000426474 E3911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr8:110504177 G>A maps to ENST00000426474 Q3397Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr8:110456058 G>A maps to ENST00000426474 P1573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr8:110477196 T>C maps to ENST00000426474 H2712H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:43243232 C>T maps to NM_181805.1 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr20:43246969 C>T maps to NM_181805.1 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:155265066 C>T maps to ENST00000423816 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr1:155264088 C>A maps to ENST00000423816 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr1:155271102 C>G maps to ENST00000423816 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:72500974 C>A maps to ENST00000419739 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr16:3025756 G>A maps to NM_004203.4 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr16:3026844 G>A maps to NM_004203.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr19:14580221 C>T maps to NM_213560.1 F688F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:89290037 G>A maps to NM_006256.2 V796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:89225996 G>T maps to NM_006256.2 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr9:131469233 G>T maps to NM_013355.3 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr9:131469664 G>A maps to NM_013355.3 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr9:131475650 C>T maps to NM_013355.3 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr9:131482296 G>C did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr9:131482818 C>T maps to NM_013355.3 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr9:131482232 C>T maps to NM_013355.3 I771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr21:44441525 C>G maps to NM_004571.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr11:125281667 G>A maps to NM_022062.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr11:125221257 C>A maps to NM_022062.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr11:125237799 C>G maps to NM_022062.2 S49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr1:201292250 C>T maps to NM_000299.3 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr12:33031141 G>T maps to NM_004572.3 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr12:32955490 C>A did not map to a codon.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr12:32975424 G>A maps to NM_004572.3 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:397292 C>T maps to NM_007183.2 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr11:397661 G>A maps to NM_007183.2 Q356Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr11:403946 G>A maps to NM_007183.2 T694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr2:159519803 C>T maps to NM_003628.3 I808I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr2:159499162 C>T maps to NM_003628.3 R621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr2:159481625 C>T maps to NM_003628.3 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr2:159481496 G>A maps to NM_003628.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:110635613 A>G maps to NM_030821.4 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr16:68293105 C>G maps to NM_012320.3 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr16:68279379 C>T maps to NM_012320.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:68293166 C>T maps to NM_012320.3 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:63357634 C>T maps to NM_001128203.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:120759996 C>A maps to NM_000928.2 *149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr1:20474794 C>T maps to NM_022819.3 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:20474749 C>T maps to NM_022819.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr22:31536232 G>A maps to NM_015715.3 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr22:31536025 C>T maps to NM_015715.3 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr22:31533773 G>A maps to NM_015715.3 Q330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:186946810 G>T maps to NM_024420.2 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:186934580 C>G maps to NM_024420.2 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr1:186934572 C>T maps to NM_024420.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr19:48556258 C>A maps to NM_003706.2 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr19:48551635 G>T maps to NM_003706.2 Y530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr19:48551599 C>G maps to NM_003706.2 *542Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr19:48601510 C>T maps to NM_003706.2 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr19:48551619 G>A maps to NM_003706.2 R536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr15:42360936 C>T maps to NM_178034.3 A811A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:42281679 G>A maps to NM_001080490.1 F523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr15:42298241 G>A maps to NM_001080490.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr15:42447754 C>T maps to ENST00000397272 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:42436660 G>A maps to ENST00000397272 F656F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr15:42434262 G>A maps to ENST00000397272 V825V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr15:42439885 C>A maps to ENST00000397272 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:42439846 C>G maps to ENST00000397272 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:42439855 C>T maps to ENST00000397272 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr15:42436765 G>T maps to ENST00000397272 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr1:20412657 C>T maps to NM_000929.2 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:20412630 G>A maps to NM_000929.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr22:38541623 C>T maps to NM_003560.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr22:38522379 C>T maps to NM_003560.2 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr22:38509520 C>T maps to NM_003560.2 K725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr22:38539188 G>A maps to NM_003560.2 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr6:46678359 G>A maps to NM_001168357.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr2:160813126 C>G maps to NM_007366.4 L972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:160869837 G>A maps to NM_007366.4 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr2:160833208 G>A maps to NM_007366.4 F808F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr2:160840458 G>C maps to NM_007366.4 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr2:160869837 G>A maps to NM_007366.4 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr9:26935119 G>A maps to NM_001031689.2 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr9:26920232 C>A maps to NM_001031689.2 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:133700498 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr8:57078999 T>C maps to NM_002655.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr8:57079983 C>T maps to NM_002655.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr8:57080765 C>T maps to NM_002655.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr8:57080765 C>T maps to NM_002655.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr20:30784257 C>T maps to NM_002657.3 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr8:42045070 G>A maps to NM_000930.3 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr8:42036453 C>A maps to NM_000930.3 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr19:44169568 G>T maps to NM_002659.2 S70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr19:44156404 A>G maps to NM_002659.2 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr2:28761223 G>C maps to NM_153021.4 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr2:28805333 C>G maps to NM_153021.4 Y565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr2:28843818 T>C maps to NM_153021.4 N1167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr2:28849332 C>G maps to NM_153021.4 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:28840616 T>C maps to NM_153021.4 C1073C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr12:14689622 G>A maps to NM_024829.5 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr12:113826394 C>G maps to NM_173542.3 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr20:8678318 G>C maps to NM_015192.2 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr20:8637883 C>T maps to NM_015192.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr15:40586547 G>A maps to NM_004573.2 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr15:40590829 G>C maps to NM_004573.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr15:40594184 G>C maps to NM_004573.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr15:40594233 C>T did not map to a codon.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr15:40581092 G>A maps to NM_004573.2 Y1127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:64023081 C>T maps to NM_000932.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:64030226 C>T maps to NM_000932.2 Q768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr11:64035012 G>A maps to NM_000932.2 E1230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr11:64032896 C>T maps to NM_000932.2 V986V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:64033996 C>T maps to NM_000932.2 I1129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:64033620 C>T maps to NM_000932.2 V1071V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:64033996 C>T maps to NM_000932.2 I1129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:64026395 C>G maps to NM_000932.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr11:64029113 C>T maps to NM_000932.2 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:64023901 C>T maps to NM_000932.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:64029984 C>T maps to NM_000932.2 F715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr11:64023012 C>T maps to NM_000932.2 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr20:9391690 G>A maps to NM_001172646.1 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr20:9459590 G>A maps to NM_001172646.1 V1173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr20:9453490 G>A maps to NM_001172646.1 K1135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr3:38050814 G>A maps to NM_001130964.1 Y539Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr3:38058109 G>T maps to NM_001130964.1 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr3:38049631 C>G maps to NM_001130964.1 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:43195689 G>A maps to NM_133373.3 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:43196284 C>T maps to NM_133373.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr17:43195396 C>T maps to NM_133373.3 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:219498428 C>T maps to ENST00000432688 F549F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:96058152 C>T maps to ENST00000371380 R1729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr10:96014053 A>G maps to ENST00000371380 Q1129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr10:96025624 C>T maps to ENST00000371380 P1397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr10:96006248 G>A maps to ENST00000371380 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr10:96018854 C>G maps to ENST00000371380 L1254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr10:95931031 C>T maps to ENST00000371380 Q530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:96030321 C>A maps to ENST00000371380 S1490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr10:95791021 C>G maps to ENST00000371380 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:39793949 C>T maps to NM_002660.2 N484N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr20:39798875 G>A maps to NM_002660.2 K925K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr20:39788555 G>A maps to NM_002660.2 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr20:39794163 C>T maps to NM_002660.2 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:81934315 G>A maps to NM_002661.2 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr16:81969813 G>A maps to NM_002661.2 T961T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:81960751 C>G maps to NM_002661.2 S828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr16:81914555 G>A maps to NM_002661.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr16:81953250 C>G maps to NM_002661.2 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:155232673 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr3:155212181 G>T maps to ENST00000340059 R661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr3:155208657 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr3:155215190 C>T maps to ENST00000340059 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:155200689 G>C maps to ENST00000340059 S1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr3:155199506 A>G maps to ENST00000340059 H1444H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:155199035 C>T maps to ENST00000340059 K1601K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr3:155232568 G>A maps to ENST00000340059 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr3:155200467 G>C maps to ENST00000340059 S1124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr3:155203499 C>G did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:155311785 C>T maps to ENST00000340059 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:155210580 C>G maps to ENST00000340059 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr3:155311743 C>T maps to ENST00000340059 Q140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr1:2411266 C>T maps to NM_014638.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr1:2436147 C>A maps to NM_014638.2 P1249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr1:2422767 A>T maps to NM_014638.2 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr2:198948627 C>A maps to NM_006226.3 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:198968661 T>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:198948699 C>G maps to NM_006226.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr2:198948699 C>T maps to NM_006226.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr2:198950568 T>C maps to NM_006226.3 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr3:17056198 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:17053636 G>A maps to NM_001144382.1 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr3:17052784 T>C maps to NM_001144382.1 N645N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:215977 C>G did not map to a codon.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr23:208185 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:209799 A>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr23:205418 G>T did not map to a codon.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr3:111426851 C>T maps to ENST00000312791 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr3:111426926 G>A maps to ENST00000312791 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr5:41381992 C>A maps to NM_001005473.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr5:41382414 C>A maps to NM_001005473.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr5:41382523 G>C maps to NM_001005473.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr5:41382447 G>A maps to NM_001005473.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:18876380 G>A maps to ENST00000266505 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr12:18876446 G>A maps to ENST00000266505 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr3:171427405 G>C maps to NM_002662.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr3:171404523 G>A maps to NM_002662.3 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr3:171405269 C>T maps to NM_002662.3 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:171427486 T>C maps to NM_002662.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr3:171405265 C>A maps to NM_002662.3 G550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr17:4725183 C>T maps to NM_002663.3 N853N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr17:4718856 G>A maps to NM_002663.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:4712419 C>T maps to NM_002663.3 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr19:40880473 C>T maps to NM_012268.2 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:40872414 G>T maps to NM_012268.2 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr19:40880509 G>A maps to NM_012268.2 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr19:40872759 A>G maps to NM_012268.2 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr14:105397200 G>A maps to NM_138790.2 Q280Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:105397101 C>T maps to NM_138790.2 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr14:105397279 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:242253335 C>T maps to NM_152666.2 R477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr1:242287804 G>A maps to NM_152666.2 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr17:17106257 G>A maps to NM_178836.3 Y194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr8:144997121 G>C maps to NM_201380.2 L2462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr8:145013595 C>A maps to NM_201384.1 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr8:144993272 G>A maps to NM_201380.2 I3709I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr8:144994321 C>A maps to NM_201380.2 E3360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:145004381 C>A maps to NM_201380.2 E985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:144993917 G>A maps to NM_201380.2 L3494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr8:144991922 G>T maps to NM_201380.2 L4159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr8:144993566 G>A maps to NM_201380.2 I3611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr8:144997294 C>A maps to NM_201380.2 E2405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr8:144997376 C>T maps to NM_201380.2 L2377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr8:144997247 C>G maps to NM_201380.2 L2420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr8:144991022 G>A maps to NM_201380.2 I4459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr8:144990866 C>A maps to NM_201380.2 L4511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr8:144992366 G>C maps to NM_201380.2 L4011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr8:145007405 G>A maps to NM_201380.2 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr8:144992843 C>T maps to NM_201380.2 L3852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr8:145004319 G>A maps to NM_201380.2 A1005A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr8:144995666 G>A maps to NM_201380.2 V2911V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr8:144994628 C>T maps to NM_201380.2 L3257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr8:144991703 C>T maps to NM_201380.2 T4232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr8:145010164 C>T maps to NM_201380.2 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr8:144991214 G>A maps to NM_201380.2 I4395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr2:68607461 G>C maps to NM_002664.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:68592491 A>G maps to NM_002664.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr2:68613705 C>A maps to NM_002664.2 S182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr2:68613715 C>T maps to NM_002664.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr14:67862285 C>A maps to NM_016445.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:124152832 C>T maps to NM_021622.4 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:179365832 C>T maps to NM_019091.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:49357479 C>T maps to NM_020904.2 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:49362155 G>A maps to NM_020904.2 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr19:49362895 G>A maps to NM_020904.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr12:19427659 G>C maps to ENST00000429027 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:19427758 C>G maps to ENST00000429027 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr12:19512470 C>T maps to ENST00000429027 F1153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr12:19406894 C>T maps to ENST00000429027 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:19285327 T>C maps to ENST00000429027 D57D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr1:204226674 G>A maps to ENST00000367191 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:204214818 G>A maps to ENST00000367191 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr1:204197244 C>T maps to ENST00000367191 A1019A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:204216507 G>C maps to ENST00000367191 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:16812670 G>A maps to ENST00000448080 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr11:16822592 C>G maps to ENST00000448080 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:16838391 G>A maps to ENST00000448080 I607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr11:16838553 C>G maps to ENST00000448080 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr7:30102286 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr7:30094399 C>G maps to ENST00000440706 S317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:45567362 C>T maps to ENST00000256692 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr12:45567170 C>G maps to ENST00000256692 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:73361615 G>A maps to NM_021200.2 W38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:131904339 C>T maps to ENST00000409158 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr2:131890542 C>G maps to ENST00000409158 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr2:131890539 G>A maps to ENST00000409158 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr19:30164907 C>T maps to ENST00000436066 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr8:96166421 C>G maps to NM_024613.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr6:151054825 C>G maps to NM_001029884.1 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr6:151116990 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:151140851 G>A maps to NM_001029884.1 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr6:151055092 A>G maps to NM_001029884.1 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr6:151116997 G>T maps to NM_001029884.1 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr19:39907573 G>A maps to NM_022835.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr14:65197534 G>T maps to ENST00000394691 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr14:65210003 G>T maps to ENST00000394691 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr14:65203598 C>G maps to ENST00000394691 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr14:65198191 C>T maps to ENST00000394691 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr14:65197403 C>T maps to ENST00000394691 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr14:65197645 C>G maps to ENST00000394691 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr16:67314064 C>T maps to NM_001129729.1 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:67316737 C>T maps to NM_001129729.1 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr16:67314150 G>A maps to NM_001129729.1 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr16:67322217 G>A maps to NM_001129729.1 L1123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:67314369 G>A maps to NM_001129729.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr16:67322085 G>A maps to NM_001129729.1 A1079A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr5:156990 C>A maps to NM_052909.3 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:155045 G>A maps to NM_052909.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr5:169622 C>T maps to NM_052909.3 H859H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr5:169463 G>A maps to NM_052909.3 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr1:6530628 C>T maps to NM_198681.2 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr1:6579503 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:6529487 C>T maps to NM_198681.2 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:6529202 C>T maps to NM_198681.2 E793E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:6534520 A>C maps to NM_198681.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr12:6428002 C>T maps to NM_001144856.1 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr12:6435719 C>T maps to NM_001144856.1 Q551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr12:6435659 C>A maps to NM_001144856.1 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr12:6436605 C>T maps to NM_001144856.1 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr12:6426765 C>T maps to NM_001144856.1 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr12:6422937 C>T maps to NM_001144856.1 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr12:93149619 G>A maps to NM_001004330.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr12:93162805 C>T maps to NM_001004330.2 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr14:68040039 G>C maps to NM_020715.2 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr14:68040015 C>G maps to NM_020715.2 Y584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr14:68040538 C>T maps to NM_020715.2 Q621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr14:68043122 C>G maps to NM_020715.2 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:43919691 C>T maps to NM_172069.3 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:43968149 C>G maps to NM_172069.3 L1063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:43992599 C>T maps to NM_172069.3 Q1449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr2:43927131 A>G maps to NM_172069.3 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr17:40823046 C>G maps to NM_024927.4 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr17:40823446 C>T maps to NM_024927.4 Q402Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:40826421 G>A maps to NM_024927.4 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:43522897 C>G maps to NM_014798.2 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:43515224 C>T maps to NM_014798.2 *1057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr17:43535727 G>A maps to NM_014798.2 H462H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:43552875 G>C maps to NM_014798.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:43516841 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:16060299 C>T maps to ENST00000420314 L1080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr1:16053703 G>A maps to ENST00000420314 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:208795687 G>A maps to NM_001080475.2 F616F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr2:208795687 G>A maps to NM_001080475.2 F616F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr1:909229 G>A maps to ENST00000379409 Q536Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:150131672 C>G maps to ENST00000443480 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:150128297 G>C maps to ENST00000443480 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:65157297 G>A maps to NM_025201.4 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:161127485 C>T maps to NM_000301.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr6:161139344 T>A maps to NM_000301.3 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr6:161173195 G>A maps to NM_000301.3 E725E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr15:90210390 G>A maps to NM_002666.4 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr9:19119734 A>T maps to NM_001122.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr9:19119763 C>A maps to NM_001122.2 G221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr9:19126307 C>T did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:4839527 G>A maps to NM_005817.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr19:4859607 C>A maps to NM_005817.4 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr19:4859625 G>A maps to NM_005817.4 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr19:4510854 G>A maps to NM_001080400.1 N1025N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr19:4511892 C>G maps to NM_001080400.1 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:4504532 G>A maps to NM_001080400.1 Q1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr19:4512045 C>T maps to NM_001080400.1 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr19:4512189 C>T maps to NM_001080400.1 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr19:4529828 C>T maps to NM_001013706.2 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr19:4523683 C>T maps to NM_001013706.2 Q416Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr19:4529858 G>A maps to NM_001013706.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr16:23700963 C>T maps to NM_005030.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:23700834 C>T maps to NM_005030.3 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:23700963 C>T maps to NM_005030.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:45268644 G>A maps to NM_004073.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:45269323 C>T maps to NM_004073.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr1:45266607 C>T maps to NM_004073.2 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:45266519 C>T maps to NM_004073.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:45271193 C>T maps to NM_004073.2 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:45266576 C>T maps to NM_004073.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:45267307 C>T maps to NM_004073.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr1:45271310 C>A maps to NM_004073.2 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr4:128806935 C>G maps to NM_014264.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr16:57290893 G>A maps to NM_015993.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:12009945 C>T maps to ENST00000376369 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr1:12017945 C>T maps to ENST00000376369 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr3:145806414 C>T maps to NM_182943.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:145828197 G>A maps to NM_182943.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr7:100860028 C>A maps to NM_001084.4 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:100856158 G>A maps to NM_001084.4 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr7:100859191 C>A maps to NM_001084.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr7:100860034 C>A maps to NM_001084.4 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr7:100859191 C>T maps to NM_001084.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:103042840 C>A did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr23:49030734 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr23:49030735 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr23:49029744 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:49028420 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr4:155458436 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr3:142403176 G>A maps to NM_001172312.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr3:142413338 G>A maps to NM_001172312.1 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr3:142413338 G>A maps to NM_001172312.1 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr23:114871236 C>G did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr23:114869354 G>C did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:114869217 C>G did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr23:114869258 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr23:114856613 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr23:114877630 G>C did not map to a codon.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr3:146167019 G>A maps to ENST00000497985 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr17:7296111 C>A maps to NM_020360.2 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr3:145914487 C>T maps to NM_020353.2 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:146311796 C>T maps to NM_001085420.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr3:146311796 C>G maps to NM_001085420.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr20:31825633 C>T maps to NM_130852.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:17471605 G>A maps to NM_031310.1 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr19:17476790 C>T maps to NM_031310.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:37265611 G>A maps to NM_020405.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:20436812 C>T maps to NM_032812.7 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr10:20506402 C>T maps to NM_032812.7 R391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr10:20534408 C>G maps to NM_032812.7 S483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr10:20453395 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:20534352 C>T maps to NM_032812.7 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:126724991 C>T maps to NM_032242.3 F656F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr3:126708281 C>T maps to NM_032242.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:126722264 C>T maps to NM_032242.3 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:126748843 T>C maps to NM_032242.3 R1666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:126747834 G>A did not map to a codon.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr3:126751292 G>A maps to NM_032242.3 K1765K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr3:126748784 C>T maps to NM_032242.3 L1647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr3:126722225 C>T maps to NM_032242.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr3:126735362 G>A maps to NM_032242.3 R1006R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:208390235 C>T maps to NM_025179.3 K344K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:208252745 G>C maps to NM_025179.3 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr1:208234157 C>A maps to NM_025179.3 E871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr1:208206831 G>A maps to NM_025179.3 G1629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr1:208391158 G>A maps to NM_025179.3 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:208206822 G>A maps to NM_025179.3 D1632D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr1:208213010 C>T maps to NM_025179.3 L1485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:208216441 C>T maps to NM_025179.3 P1327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:208269444 C>G maps to NM_025179.3 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr23:153697281 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr23:153696317 C>G did not map to a codon.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr23:153697419 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr23:153688601 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr23:153688731 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:153699941 C>T did not map to a codon.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr23:153691834 G>T did not map to a codon.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr23:153694504 G>A did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr23:153697266 G>C did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr23:153697779 G>C did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:153695957 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:153696527 C>G did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr7:132192483 G>A maps to NM_020911.1 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr7:131872352 G>C maps to NM_020911.1 S957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr7:131887530 G>A maps to NM_020911.1 D820D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr7:131825371 C>T maps to NM_020911.1 K1808K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:131866166 G>C maps to NM_020911.1 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr7:131864506 C>T maps to NM_020911.1 L1271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr7:131853319 G>A maps to NM_020911.1 Y1343Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr7:132192498 C>A maps to NM_020911.1 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr3:48462782 G>C maps to NM_001130082.1 S555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr3:48445991 G>A maps to NM_001130082.1 I2103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr3:48453975 G>A maps to NM_001130082.1 Y1636Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr3:48455393 C>T maps to NM_001130082.1 R1432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr3:48462745 T>C maps to NM_001130082.1 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:48447187 G>A maps to NM_001130082.1 L2082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr3:48463745 C>T maps to NM_001130082.1 Q471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:48454571 C>T maps to NM_001130082.1 K1514K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr3:48465156 C>A maps to NM_001130082.1 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr22:50728887 G>C maps to NM_012401.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:50721498 G>A maps to NM_012401.2 L932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:50719196 C>T maps to NM_012401.2 L1323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr22:50720303 G>A maps to NM_012401.2 V1108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr22:50727978 G>A maps to NM_012401.2 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr22:50716924 G>A maps to NM_012401.2 I1557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr22:50717350 C>T maps to NM_012401.2 K1493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr22:50726222 C>A did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr22:50714135 G>C maps to NM_012401.2 L1838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr22:50719850 G>A maps to NM_012401.2 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:153040416 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr23:153035385 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr23:153043510 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr23:153038979 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr23:153036249 A>T did not map to a codon.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr23:153036250 G>T did not map to a codon.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr23:153043090 G>A did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr23:153037012 G>A did not map to a codon.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr23:153033835 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr23:153044064 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr23:153039008 A>G did not map to a codon.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr12:94648978 G>A maps to NM_005761.1 E998E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr12:94543415 C>G maps to NM_005761.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:94631549 G>A maps to NM_005761.1 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr12:94641866 G>A maps to NM_005761.1 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr3:129280746 C>T did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:129282029 G>A maps to NM_015103.2 I1525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr3:129324822 G>A maps to NM_015103.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:129288722 G>A maps to NM_015103.2 I1276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:129293325 G>A maps to NM_015103.2 V846V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr3:129290521 G>C maps to NM_015103.2 V1081V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr3:129303366 G>C maps to NM_015103.2 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr3:129289673 C>T maps to NM_015103.2 S1235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr3:129285419 G>A maps to NM_015103.2 Q1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:129275928 C>T maps to NM_015103.2 S1861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr1:205819092 C>T maps to NM_152491.4 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:205819035 C>T maps to NM_152491.4 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:205799454 G>A maps to NM_152491.4 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr6:89855955 C>T maps to NM_001010853.1 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr6:89855890 G>T maps to NM_001010853.1 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:156182916 C>T maps to NM_007221.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:72174472 C>T maps to NM_031293.2 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr16:72166659 C>T maps to NM_031293.2 Q478Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr16:72166805 C>A maps to NM_031293.2 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr15:74327529 G>A maps to NM_033239.2 E576E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr22:41985779 C>T maps to NM_002676.2 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr22:41980551 G>A maps to NM_002676.2 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:41973847 G>A maps to NM_002676.2 F210F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-MV-A51V-01A-11D-A26M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:8941603 C>T maps to NM_000303.2 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr16:8891771 C>T maps to NM_000303.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr9:139309088 C>T maps to NM_015160.1 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr9:139316354 C>T maps to NM_015160.1 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:102939933 G>A maps to NM_004279.2 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr7:102939127 G>A maps to NM_004279.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr2:190728531 A>G maps to NM_000534.4 E640E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr7:6042260 G>A maps to NM_000535.5 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr7:6035258 G>T maps to NM_000535.5 S270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr23:152937615 G>A did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:152937345 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr23:152939598 G>C did not map to a codon.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr23:152937059 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:152938057 C>A did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:152935945 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:219137298 C>T maps to NM_001077399.2 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:219209679 G>A maps to NM_015488.4 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr19:50365342 G>C maps to NM_007254.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:50367630 G>A maps to NM_007254.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr6:160239665 C>T maps to NM_173516.1 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr6:160225084 C>T maps to NM_173516.1 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr6:160221822 G>C maps to NM_173516.1 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:160232767 C>T maps to NM_173516.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr6:160239601 C>T maps to NM_173516.1 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr6:160240102 C>G maps to NM_173516.1 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr10:118314750 C>T maps to NM_000936.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr10:118321148 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:118310641 C>A maps to NM_000936.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr10:118305636 G>A maps to NM_000936.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr10:118314963 T>A maps to NM_000936.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr10:118350685 C>A maps to NM_006229.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:118350644 C>T maps to NM_006229.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr10:118351364 T>A maps to NM_006229.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr10:118360681 C>T maps to NM_006229.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr10:118364951 T>C maps to NM_006229.2 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:118394391 C>T maps to NM_005396.4 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr10:118380837 C>T maps to NM_005396.4 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:118228770 T>C maps to NM_001011709.2 N334N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr10:118225614 G>T maps to NM_001011709.2 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr14:74179619 C>T maps to NM_006029.4 E241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr14:74179295 C>T maps to NM_006029.4 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr8:26365182 G>A maps to NM_007257.5 D363D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr23:152226003 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr23:152159940 C>A did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr23:152159942 A>G did not map to a codon.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr23:152159038 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:46973830 C>A maps to NM_018215.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:46973746 G>A maps to NM_018215.3 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr19:46997597 G>A maps to NM_020709.1 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr19:46997246 G>A maps to NM_020709.1 A492A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-E7-A3X6-01A-12D-A22Z-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr19:46998593 G>A maps to NM_020709.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr17:37824886 C>T maps to NM_002686.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr17:37826296 G>A maps to NM_002686.3 G168G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-K4-A6MB-01A-11D-A31L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:28196681 C>A maps to NM_006228.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr8:28186801 T>G did not map to a codon.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr6:36261950 C>T maps to NM_001145716.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr11:823703 C>T maps to NM_020376.3 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr22:44342252 G>A maps to NM_025225.2 K479K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr23:7870170 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr23:7870135 A>G did not map to a codon.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr22:44282274 C>T maps to ENST00000216177 W286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr22:44285325 G>A maps to ENST00000216177 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:7615489 G>A maps to NM_001166111.1 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr19:7601417 C>G maps to NM_001166111.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr19:7614809 C>T maps to NM_001166111.1 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr19:7615303 C>T maps to NM_001166111.1 R654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr9:140354927 C>A maps to NM_001098537.1 E1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:140441821 G>C maps to NM_001098537.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr9:140357879 G>A maps to NM_001098537.1 I1110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr9:140437933 C>T maps to NM_001098537.1 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr17:46024054 C>G maps to NM_018129.3 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr2:55895070 T>C maps to NM_033109.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:55882033 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr2:55870294 G>A maps to NM_033109.3 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr3:52183971 G>C maps to NM_015426.4 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr3:52109917 C>T maps to NM_015426.4 Q403Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:52172280 C>T maps to NM_015426.4 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:74970316 G>C maps to NM_001099271.1 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr5:74970364 C>A maps to NM_001099271.1 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr5:74981250 T>C maps to NM_001099271.1 E396E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:53546443 G>T maps to NM_153703.4 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:53537229 C>T maps to NM_153703.4 Y160Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:53544159 G>A maps to NM_153703.4 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:53546485 G>A maps to NM_153703.4 K581K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr7:131191391 G>A maps to NM_001018111.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:131189122 G>A maps to NM_001018111.2 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr3:127379998 G>A maps to NM_015720.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:84561207 C>A did not map to a codon.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr23:84634270 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr23:84560910 A>G did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:84560833 A>T did not map to a codon.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr20:30803205 T>C maps to NM_015352.1 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr20:30804434 C>T maps to NM_015352.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr20:30803175 G>A maps to NM_015352.1 W117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr21:46685468 C>T maps to NM_133635.4 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr1:166819003 G>C maps to NM_017542.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:166818539 C>T maps to NM_017542.3 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr1:166818580 G>A maps to NM_017542.3 K255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:166818871 G>A maps to NM_017542.3 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:151378786 G>A maps to NM_015100.3 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:151378585 C>T maps to NM_015100.3 V975V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:151403212 G>A maps to NM_015100.3 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr23:24906200 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr23:24759576 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:24760145 G>A did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:24833164 G>A did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr23:24859797 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:24906224 A>G did not map to a codon.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr23:24759499 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:24766500 G>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr11:65061698 C>T maps to NM_002689.2 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr11:65036195 C>G maps to NM_002689.2 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr11:65063046 C>G maps to NM_002689.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr11:65046237 C>T maps to NM_002689.2 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:65048485 G>A maps to NM_002689.2 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:50905128 C>G maps to ENST00000391817 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr22:42991565 G>A maps to ENST00000415122 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr22:42981856 G>C maps to ENST00000415122 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr12:133245251 C>T maps to ENST00000455752 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:133226442 C>T maps to ENST00000455752 P1208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:133201511 G>A maps to ENST00000455752 F2245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:133257722 C>T did not map to a codon.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr12:133238237 C>T maps to ENST00000455752 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAME-01A-12D-A42E-08 chr12:133219171 C>T maps to ENST00000455752 W1627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:133252081 T>A maps to ENST00000455752 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr14:50118049 T>C maps to NM_002692.3 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr2:75196536 T>C maps to NM_019896.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr15:89873443 C>T maps to NM_002693.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:89867415 C>A maps to NM_002693.2 G664G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr15:89873434 G>A maps to NM_002693.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr15:89865191 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:43565466 C>T maps to NM_006502.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:43571700 C>T maps to NM_006502.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:43555014 G>A maps to NM_006502.2 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr6:43581701 C>G maps to NM_006502.2 S517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr6:43565431 G>T did not map to a codon.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr18:51818252 C>T maps to NM_007195.2 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr18:51820662 A>C maps to NM_007195.2 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:74892359 G>A maps to NM_016218.2 E614E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:74892398 C>T maps to NM_016218.2 C627C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr10:103343417 C>T maps to NM_013274.3 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr10:103343315 G>A maps to NM_013274.3 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr10:103343318 G>A maps to NM_013274.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr7:44112895 G>A maps to NM_013284.2 N493N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:44119253 G>C maps to NM_013284.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr7:44113618 G>A maps to NM_013284.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:44119559 T>A did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr4:2130960 C>G maps to NM_181808.2 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:2172899 G>C maps to NM_181808.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr4:2214797 C>T maps to NM_181808.2 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr4:2210145 G>C maps to NM_181808.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr3:121207488 A>T maps to ENST00000393672 L1566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:121206873 G>C maps to ENST00000393672 S1771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr3:121208085 G>C maps to ENST00000393672 S1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:121207034 C>T maps to ENST00000393672 K1717K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr3:121258346 G>C maps to ENST00000393672 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:121215687 G>A maps to ENST00000393672 Q885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr3:121168258 G>A maps to ENST00000393672 I2525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr3:121251879 G>T maps to ENST00000393672 S439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr3:121206401 C>T maps to ENST00000393672 G1928G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:121228969 G>A maps to ENST00000393672 Q714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr3:121228937 C>T maps to ENST00000393672 W724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr3:121260198 G>C maps to ENST00000393672 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr3:121155014 G>A maps to ENST00000393672 F2635F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:86305368 C>T maps to NM_015425.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr2:86266518 G>C maps to NM_015425.3 L1269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr2:86258590 C>G maps to NM_015425.3 L1480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr2:86258742 C>A maps to NM_015425.3 E1430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr2:86325856 A>C maps to NM_015425.3 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:86315960 G>T maps to NM_015425.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr2:86254602 G>A maps to NM_015425.3 V1702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:86280075 C>T maps to NM_015425.3 A752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr2:86254638 G>A maps to NM_015425.3 H1690H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr2:86255101 T>C maps to NM_015425.3 P1656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:86258484 G>A maps to NM_015425.3 Q1516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:113330229 G>A maps to NM_019014.4 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:113310242 G>A maps to NM_019014.4 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr6:43488983 G>A maps to NM_203290.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr13:28239828 G>A maps to NM_152705.1 K36K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:7401069 C>T maps to NM_000937.4 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr17:7405418 G>T maps to NM_000937.4 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr17:7401048 G>A maps to NM_000937.4 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr17:7412381 C>G maps to NM_000937.4 V1195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:7415536 G>T maps to NM_000937.4 E1456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr17:7388151 C>T maps to NM_000937.4 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr17:7415625 G>A maps to NM_000937.4 E1485E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr17:7399871 G>A maps to NM_000937.4 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr4:57889712 C>G maps to NM_000938.1 L911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr4:57852589 C>T maps to NM_000938.1 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr16:57500099 C>T maps to NM_032940.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr19:1090944 G>A maps to NM_002695.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr22:38355471 G>T maps to ENST00000407936 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr11:62533725 C>T maps to NM_002696.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr11:62532661 C>G maps to NM_002696.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:840377 C>T maps to NM_021128.4 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr10:79743751 C>A maps to NM_007055.3 E1119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:79777454 G>A maps to NM_007055.3 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr10:79770262 T>C maps to NM_007055.3 E536E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr10:79745842 G>A maps to NM_007055.3 N992N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr10:79781630 C>T maps to NM_007055.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr10:79781642 G>A maps to NM_007055.3 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr10:79784792 C>T maps to NM_007055.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr10:79740027 C>A maps to NM_007055.3 E1299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr10:79785920 C>T maps to NM_007055.3 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr10:79759834 G>A maps to NM_007055.3 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:106770205 G>C maps to NM_018082.5 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr12:106903236 C>T maps to NM_018082.5 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:106804614 C>T maps to NM_018082.5 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:145608195 C>T maps to NM_006468.6 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr1:145601613 G>A maps to NM_006468.6 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:22337526 C>G maps to NM_018119.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr16:22319515 C>G maps to NM_018119.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr1:145457095 C>T maps to NM_032305.1 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr22:41928096 C>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr22:41936730 G>A maps to NM_138338.3 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr19:630112 C>T maps to NM_005035.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr19:622695 C>T maps to NM_005035.3 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr19:633452 G>T maps to NM_005035.3 C20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:621834 C>A maps to NM_005035.3 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:622749 G>C maps to NM_005035.3 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr19:621792 C>A maps to NM_005035.3 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr19:619038 G>A maps to NM_005035.3 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:629860 C>G maps to NM_005035.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr19:619083 G>A maps to NM_005035.3 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr7:72413603 G>A maps to ENST00000434423 T1024T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr7:72413258 G>A maps to ENST00000434423 T909T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr7:72412578 C>T maps to ENST00000434423 Q683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:75048153 G>C maps to ENST00000257665 S1205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr7:75066939 G>A maps to ENST00000257665 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr7:53103780 C>T maps to NM_182595.3 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:53104098 C>T maps to NM_182595.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr7:53104149 C>T maps to NM_182595.3 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:53103681 C>G maps to NM_182595.3 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr7:53103862 C>T maps to NM_182595.3 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr2:25384042 G>A maps to NM_001035256.1 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:46662723 G>A maps to ENST00000371986 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr1:46657835 G>A maps to ENST00000371986 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr7:76254891 C>T maps to NM_012230.3 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr7:94947685 G>A maps to NM_000446.5 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr7:94947685 G>A maps to NM_000446.5 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr7:95041044 A>G maps to NM_000305.2 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr7:94989395 G>A maps to NM_000940.2 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr7:94993186 G>T maps to NM_000940.2 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr8:99169961 G>A maps to NM_015029.2 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr19:30101461 G>A maps to NM_006627.2 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr19:30106175 C>T maps to NM_006627.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:121018921 G>A maps to NM_015918.3 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:100304473 C>T maps to NM_005837.2 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr7:100304611 G>A maps to NM_005837.2 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr3:119367223 G>A maps to NM_022135.2 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr6:105609535 T>C maps to NM_022361.4 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr7:75615696 C>A maps to NM_000941.2 Y647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr7:75609787 C>T maps to NM_000941.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr7:75615553 C>G maps to NM_000941.2 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:75612891 G>A maps to NM_000941.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:48372643 G>A did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:48372634 C>T did not map to a codon.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr13:38164577 C>T maps to NM_006475.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr13:38164583 C>G maps to NM_006475.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:38154009 C>A maps to NM_006475.2 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr7:124475364 T>A maps to NM_015450.2 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr7:124467276 G>T maps to NM_015450.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr7:124493145 G>C maps to NM_015450.2 S250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr7:124475436 C>T maps to NM_015450.2 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr8:43211962 C>G maps to NM_001005365.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr8:43197469 C>T maps to NM_001005365.2 N453N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr8:43197036 T>C maps to NM_001005365.2 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:43197331 C>G maps to NM_001005365.2 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr18:14537798 C>T did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr18:14543082 C>T maps to ENST00000444806 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr18:14543046 G>A maps to ENST00000444806 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr18:14542995 G>A maps to ENST00000444806 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr2:131976034 C>T maps to NM_001083538.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr2:132021607 C>T maps to NM_001083538.1 T860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr2:131976362 G>T maps to NM_001083538.1 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr2:131984403 C>G maps to NM_001083538.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr2:131995780 A>G maps to NM_001083538.1 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr2:132020956 C>T maps to NM_001083538.1 D643D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:130878028 G>C maps to NM_001099771.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:130832563 G>A maps to NM_001099771.2 F827F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:130877917 G>C maps to NM_001099771.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr14:19553775 G>A maps to NM_001005356.2 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr22:16279259 T>C maps to NM_001136213.1 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr22:16279199 A>G maps to NM_001136213.1 Y341Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr22:16287759 G>A maps to NM_001136213.1 N42N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr22:16287675 G>A maps to NM_001136213.1 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:167381394 G>A maps to NM_002697.3 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:167367229 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:167339438 T>G maps to NM_002697.3 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:42599720 G>A maps to ENST00000342301 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr19:42598044 G>C maps to ENST00000342301 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr19:42600335 G>A maps to ENST00000342301 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:42600012 G>A maps to ENST00000342301 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr11:120186098 C>G maps to NM_014352.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:120180159 C>T maps to NM_014352.2 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:120169014 C>T maps to NM_014352.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:38511338 G>C maps to NM_002699.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr2:105473458 G>C maps to NM_006236.1 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr23:82763490 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:82763833 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr23:82764167 G>A did not map to a codon.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr23:82763949 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr23:82764211 G>C did not map to a codon.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr4:147561042 G>T maps to NM_004575.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:147561908 C>T maps to NM_004575.2 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr4:147561863 C>T maps to NM_004575.2 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:31138028 C>T maps to NM_002701.4 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr8:128429169 C>T maps to NM_001159542.1 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr12:51585470 G>A maps to NM_002702.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr12:51586128 G>A maps to NM_002702.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr12:51586206 G>A maps to NM_002702.3 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr7:39125584 G>A maps to NM_007252.3 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr7:39472767 C>A maps to NM_007252.3 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:39500144 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:39247148 C>A maps to NM_007252.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr7:39472815 G>T maps to NM_007252.3 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:10221061 G>A maps to NM_001040664.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:10220323 C>T maps to NM_001040664.2 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr5:54737721 G>C maps to NM_176895.1 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr5:54721825 G>C maps to NM_176895.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:56990202 C>T maps to NM_003713.4 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr10:122334733 C>G maps to NM_001030059.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr8:38123797 G>A maps to NM_001102559.1 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr9:4663238 C>G maps to NM_203453.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr9:134165482 G>A maps to NM_032728.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr9:134165680 C>T maps to NM_032728.3 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:46628122 C>A maps to NM_001001928.2 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr22:46627867 C>T maps to NM_001001928.2 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr22:46614185 C>G maps to NM_001001928.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr6:35392458 C>T maps to NM_006238.4 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr6:35387982 C>G maps to NM_006238.4 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr6:35378950 C>T maps to NM_006238.4 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:35391852 C>A maps to NM_006238.4 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:12422875 C>G maps to NM_015869.4 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr3:12447408 C>A maps to NM_015869.4 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr3:12447543 G>C maps to NM_015869.4 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr3:12447408 C>G maps to NM_015869.4 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr3:12475472 G>A maps to NM_015869.4 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:12458486 C>T maps to NM_015869.4 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:12458420 C>G maps to NM_015869.4 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr4:23816013 G>A maps to NM_013261.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr4:23815313 T>G maps to NM_013261.3 R598R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr4:23803351 C>A did not map to a codon.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr4:23814401 T>A maps to NM_013261.3 K663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr5:149216297 C>T maps to NM_133263.3 I760I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr4:57265346 C>A maps to NM_002703.3 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr4:74853063 G>T maps to NM_002704.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:75335822 C>T maps to NM_021823.3 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr15:75340973 G>A maps to NM_021823.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr1:42922313 C>T maps to NM_024664.2 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr1:42925521 A>G maps to NM_024664.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:42922601 G>A maps to NM_024664.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:42922573 C>A maps to NM_024664.2 S113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:18797201 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr23:18822096 G>C did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:18822165 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:18822140 C>G did not map to a codon.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr23:18725942 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:18824616 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr23:18842186 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:18802021 T>C did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr4:76813006 G>A maps to NM_006239.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:76817436 C>T maps to NM_006239.2 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr4:76797580 G>A maps to NM_006239.2 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr11:70170533 C>G maps to NM_003626.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:70202352 C>T maps to NM_003626.2 Q859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr11:70170528 G>T maps to NM_003626.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:70201867 G>A maps to NM_003626.2 K813K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr11:70194496 G>T maps to NM_003626.2 E712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr11:70170994 C>A maps to NM_003626.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr12:81768547 C>G did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:82147868 A>G maps to NM_003625.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:81732973 G>A maps to NM_003625.2 R845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr12:82147792 G>A maps to NM_003625.2 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr12:81746947 C>G maps to NM_003625.2 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr12:81675141 G>A maps to NM_003625.2 Q1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:49632241 C>T maps to NM_003660.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:49639072 C>T maps to NM_003660.2 Q520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:49643308 C>T maps to NM_003660.2 R778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:49652415 G>A maps to NM_003660.2 Q1092Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr19:49649226 G>T maps to NM_003660.2 E925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:49643259 G>A maps to NM_003660.2 K761K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr19:49636504 G>A maps to NM_003660.2 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr19:49652820 C>T maps to NM_003660.2 F1124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr12:27844716 G>A maps to NM_003622.3 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr12:27829453 C>T maps to NM_003622.3 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:27817315 C>T maps to NM_003622.3 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T4-01A-11D-A391-08 chr12:27825374 C>T maps to NM_003622.3 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:7672105 C>T maps to NM_003621.2 S719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:7650751 G>C maps to NM_003621.2 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:7586920 C>T maps to NM_003621.2 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:7670062 G>A maps to NM_003621.2 K610K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr11:7661078 G>A maps to NM_003621.2 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr12:42835253 C>T maps to NM_201515.1 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr12:42840064 C>T maps to NM_016488.6 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:143767731 C>G maps to NM_001123068.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:64455080 C>T maps to NM_000942.4 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:122364491 G>A maps to NM_000943.4 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:40208913 A>T maps to NM_006112.3 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr1:40214743 C>G maps to NM_006112.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr2:170471121 C>A maps to NM_004792.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:36823786 G>A maps to NM_016059.4 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr22:22024200 G>A did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr14:50074506 C>G maps to NM_152329.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr14:50074212 G>A maps to NM_152329.3 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr6:109714029 C>G maps to NM_001111298.2 *338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr15:43873499 C>T maps to NM_001130858.2 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr15:43873493 C>T maps to NM_001130858.2 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr5:102519107 G>A maps to ENST00000451606 Q1047Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr5:102482249 G>A maps to ENST00000451606 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:4933744 C>T maps to NM_002705.4 Q1637Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:4934818 C>T maps to NM_002705.4 L1279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:4934920 C>T maps to NM_002705.4 E1245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:4933974 G>A maps to NM_002705.4 L1561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:4934724 G>A maps to NM_002705.4 L1311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:4934736 C>A maps to NM_002705.4 E1307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:4933532 G>C maps to NM_002705.4 S1708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr16:4945330 G>C maps to NM_002705.4 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:4933528 C>T maps to NM_002705.4 V1709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr14:60752364 G>A maps to NM_177952.2 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr14:60750236 C>T maps to NM_177952.2 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr2:44457785 G>T maps to NM_002706.4 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:58734120 G>A maps to NM_003620.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr17:57057638 G>A maps to NM_014906.3 E505E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr17:57057839 C>T maps to NM_014906.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr17:57057950 G>A maps to NM_014906.3 E609E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:27604600 G>A maps to NM_177983.1 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:27609063 C>T maps to NM_177983.1 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr2:27607697 C>A maps to NM_177983.1 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr2:27604473 G>A maps to NM_177983.1 R545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:63195922 G>A maps to NM_020700.1 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr12:63328393 G>A maps to NM_020700.1 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr1:113252904 G>C maps to NM_005167.5 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr4:89199465 G>A maps to NM_152542.3 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr4:89186254 G>A maps to NM_152542.3 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:160474177 C>T maps to NM_139245.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr3:160474242 G>A maps to NM_139245.2 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr11:73958133 A>G maps to NM_016147.1 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:73915403 C>T maps to NM_016147.1 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:161140555 C>T maps to NM_001122764.1 H415H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:161138283 C>T maps to NM_001122764.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:161140822 G>C did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:161140929 A>C maps to NM_001122764.1 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:161140867 C>T maps to NM_001122764.1 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:161138867 G>A maps to NM_001122764.1 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr1:161140444 G>A maps to NM_001122764.1 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr11:67168208 C>T maps to NM_001008709.1 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr2:29016736 A>G maps to NM_002709.2 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr12:111168531 G>A maps to NM_002710.2 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr6:30577697 G>C maps to NM_002714.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr6:30571978 C>A maps to NM_002714.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr6:30569833 G>A maps to NM_002714.2 V864V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr6:30573925 G>C maps to NM_002714.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr6:30035193 G>T maps to NM_021959.2 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:202411573 G>A did not map to a codon.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr1:202391783 C>G maps to ENST00000367270 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:202549681 C>G maps to NM_002481.3 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:202400647 C>T maps to ENST00000367270 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr1:202418188 C>G maps to ENST00000367270 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:55610163 C>A maps to NM_017607.2 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:55624148 C>T maps to NM_017607.2 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:55607502 G>A maps to NM_017607.2 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr14:104216223 C>T maps to NM_015316.2 Q292Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr14:104206364 T>C maps to NM_015316.2 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:45899847 G>A maps to NM_001142502.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr19:45895488 G>A maps to NM_001142502.1 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr19:45895560 C>T maps to NM_001142502.1 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:45888871 C>T maps to NM_001142502.1 E732E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr11:64012288 G>A maps to NM_138689.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr11:64012230 T>A maps to NM_138689.2 K147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr19:49377380 C>A maps to NM_014330.3 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:204379759 C>A maps to NM_032833.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:204379891 G>A maps to NM_032833.3 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:204375371 C>A maps to NM_032833.3 E664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr1:204380098 G>A maps to NM_032833.3 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr1:204380338 G>C maps to NM_032833.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr8:145726133 G>A maps to NM_032902.5 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr20:37518262 C>T maps to NM_015568.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr20:37524348 C>T maps to NM_015568.2 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr20:37464798 G>A maps to NM_015568.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr17:37791924 G>T maps to ENST00000394271 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:195251627 G>A maps to NM_006241.4 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr7:113558487 G>A maps to NM_002711.3 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr7:113558667 T>G maps to NM_002711.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr7:113518600 G>T maps to NM_002711.3 S849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr7:113519917 G>C maps to NM_002711.3 S410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr7:113522168 C>T maps to NM_002711.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr7:113558511 T>C maps to NM_002711.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr7:113518192 G>C maps to NM_002711.3 S985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr10:93389800 C>T maps to NM_005398.4 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr23:49143536 G>A did not map to a codon.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr2:242092933 G>A maps to NM_002712.1 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:28167599 C>G maps to NM_014110.4 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:28167702 C>G maps to NM_014110.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr1:28165349 A>C maps to NM_014110.4 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:28176863 C>G maps to NM_014110.4 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr7:94917927 T>C maps to NM_001166160.1 S1270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:94540504 G>A maps to NM_001166160.1 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:94539494 C>T maps to NM_001166160.1 R24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr7:94897910 G>A maps to NM_001166160.1 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr7:94540568 G>T maps to NM_001166160.1 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr7:94540584 C>G maps to NM_001166160.1 S387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:48218656 G>C maps to NM_032595.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr17:48213402 G>A maps to NM_032595.3 Q743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr5:133537631 A>G maps to NM_002715.2 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:52724376 C>T maps to NM_014225.5 F503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:52719906 G>A maps to NM_014225.5 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr19:52719117 G>T maps to NM_014225.5 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr11:111637043 C>T maps to NM_181699.2 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:111614219 G>A maps to NM_181699.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr11:111614249 G>A maps to NM_181699.2 Y468Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr11:111637043 C>T maps to NM_181699.2 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:111608255 C>T maps to NM_181699.2 V609V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr8:26227899 C>T maps to NM_001177591.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr5:146257591 G>A maps to ENST00000394414 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr5:145969707 C>T maps to ENST00000394414 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr5:145969707 C>T maps to ENST00000394414 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr4:6335372 G>A maps to NM_181876.2 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr4:6473932 C>T maps to NM_020416.3 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr4:6335435 G>A maps to NM_181876.2 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:135742026 C>A maps to NM_181897.2 S39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr3:135789354 G>C maps to NM_002718.4 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr23:301593 C>T did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr23:295188 C>G did not map to a codon.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr23:347108 C>T did not map to a codon.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr23:299629 C>A did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:306407 C>G did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr23:322193 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr23:299414 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:302112 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:306332 G>A did not map to a codon.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr11:64695311 G>A maps to NM_006244.3 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:64694349 C>T maps to NM_006244.3 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:64695612 C>T maps to NM_006244.3 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr11:64695867 C>T maps to NM_006244.3 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr11:64700271 G>A maps to NM_006244.3 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr6:42974301 C>T maps to NM_006245.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr6:42975719 C>T maps to NM_006245.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr6:42975941 C>T maps to NM_006245.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr6:42978732 C>T maps to NM_006245.2 Q557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr6:42978996 C>T maps to NM_006245.2 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr6:42979020 C>T maps to NM_006245.2 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr6:42974674 C>T maps to NM_006245.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr6:42975222 C>T maps to NM_006245.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:75230849 G>A maps to NM_001142353.1 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr8:22398213 C>A maps to ENST00000397775 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr8:22332572 G>A maps to ENST00000397775 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr8:22398299 G>A maps to ENST00000397775 K517K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr2:68408095 C>G maps to ENST00000409752 *190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr16:30096295 C>A maps to NM_002720.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:30092609 G>A maps to NM_002720.1 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr18:9595084 G>C maps to NM_001042388.1 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr18:9570271 C>A maps to NM_001042388.1 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr18:9553377 G>A maps to NM_001042388.1 Q745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr18:9570581 C>T maps to NM_001042388.1 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr18:9595102 G>C maps to NM_001042388.1 S34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr18:9550073 C>T maps to NM_001042388.1 R841R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr18:9547887 G>A maps to NM_001042388.1 Q918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr18:9588828 C>T maps to NM_001042388.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr18:9553420 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:73114034 C>G maps to NM_174907.2 S224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:73114240 C>A maps to NM_174907.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:73096399 C>T maps to NM_174907.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr14:94711958 C>T maps to NM_058237.1 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr14:94741741 C>T maps to NM_058237.1 S827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr14:94722821 A>T maps to NM_058237.1 K631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr14:94722866 C>T maps to NM_058237.1 Q646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:46890449 C>T maps to NM_006247.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr19:46891832 G>C maps to NM_006247.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr9:127920567 G>A maps to NM_001123355.1 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:244868943 G>A maps to NM_016076.3 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr1:244855253 G>T maps to NM_016076.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr22:41999385 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:103900463 G>A maps to NM_015062.3 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:103901411 G>A maps to NM_015062.3 Q1049Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr10:103899302 G>A maps to NM_015062.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr10:103899029 C>T maps to NM_015062.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr6:32130356 C>T maps to NM_138717.1 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr5:64865503 C>T maps to NM_015342.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr5:64859169 G>A maps to NM_015342.2 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr10:47087271 C>A maps to NM_005972.4 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr23:48759276 G>C did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr18:77664068 G>A maps to NM_025078.4 D241D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr18:77679371 C>T maps to NM_025078.4 W140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:19653761 C>T maps to NM_017765.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr19:8563938 C>T maps to NM_032152.4 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr22:22892461 C>T maps to NM_206954.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr22:22892643 G>A maps to NM_206954.1 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr22:22893376 G>A maps to NM_206954.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr22:22890988 G>A maps to NM_206954.1 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:12853450 C>A maps to NM_023013.2 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr1:12854213 C>A maps to NM_023013.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr1:12955519 C>T maps to NM_001039361.3 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr1:12884823 C>A maps to NM_001146344.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:12887574 T>A maps to NM_001146344.1 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:12887676 A>G maps to NM_001146344.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr1:12887379 C>T maps to NM_001146344.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:12836178 C>T maps to NM_001080830.1 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:12837468 G>T maps to NM_001080830.1 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr1:12837423 C>T maps to NM_001080830.1 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:12836108 C>G maps to NM_001080830.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:12835216 G>T maps to NM_001080830.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr1:13669147 C>T maps to ENST00000334600 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr1:13475072 C>T maps to NM_001099850.1 Q352Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr1:12918912 C>T maps to NM_023014.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:12921261 C>G maps to NM_023014.1 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:13036644 C>T maps to NM_001100631.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr1:13036287 A>C maps to NM_001100631.1 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:12939598 C>G maps to ENST00000376192 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr1:13001217 G>C maps to ENST00000415464 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr1:13001304 G>C maps to ENST00000415464 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr1:12979809 C>T maps to NM_001012277.1 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr1:12979809 C>T maps to NM_001012277.1 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr10:135164889 T>C maps to ENST00000423766 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:11547452 C>A maps to NM_006248.3 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:11546300 A>T maps to NM_006248.3 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr12:11546146 G>A maps to NM_006248.3 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr12:11420474 A>G maps to NM_006249.4 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr15:91522501 G>C maps to NM_003981.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr1:156756404 C>G maps to NM_005973.4 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr11:82550365 C>T maps to NM_199418.2 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:82560963 G>C maps to NM_199418.2 S269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr6:106552895 G>A maps to NM_001198.3 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr6:106552895 G>A maps to NM_001198.3 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr6:106553638 C>G maps to NM_001198.3 S535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr6:106553408 C>T maps to NM_001198.3 H458H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr6:106553417 C>A maps to NM_001198.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr6:106553663 C>T maps to NM_001198.3 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr11:45241210 C>T maps to NM_020229.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr9:133542070 C>T maps to NM_021619.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr6:100062613 C>T maps to ENST00000359773 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr6:100062340 C>T maps to ENST00000359773 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr8:70980526 G>A maps to NM_024504.2 Q284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr21:43298916 G>A maps to NM_022115.3 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr21:43222982 C>G maps to NM_022115.3 A1310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr21:43242384 C>A maps to NM_022115.3 A956A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:3350373 G>A maps to NM_022114.3 *1277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:3348545 G>T maps to NM_022114.3 E1180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr1:3328296 C>T maps to NM_022114.3 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:3102851 G>T maps to NM_022114.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr1:14109017 C>T maps to NM_012231.4 S1576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr1:14109249 C>T maps to NM_012231.4 Q1654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr1:14105375 T>C maps to NM_012231.4 C362C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr1:14106614 A>G maps to NM_012231.4 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr12:108128142 T>C maps to NM_012406.3 K750K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:121738026 G>A maps to NM_018699.2 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:121742373 C>A maps to NM_018699.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T4-01A-11D-A391-08 chr4:121738035 G>A maps to NM_018699.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr16:90130107 C>T maps to NM_001098173.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr16:90128809 G>A maps to NM_001098173.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:81123464 C>T maps to NM_001099403.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:81123530 C>T maps to NM_001099403.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr5:23521273 C>G maps to NM_020227.2 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:23526573 G>A maps to NM_020227.2 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr5:23527752 G>A maps to NM_020227.2 R852R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr5:23526738 G>C maps to NM_020227.2 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr5:23524553 G>T maps to NM_020227.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr5:23527593 A>C maps to NM_020227.2 T799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:45980610 G>C maps to NM_181697.1 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:12911833 G>A maps to NM_005809.4 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:12911681 G>C maps to NM_181738.1 S102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:12911748 G>A maps to NM_005809.4 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:120928688 C>T maps to NM_006793.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr23:23700609 C>G did not map to a codon.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr23:23693122 A>G did not map to a codon.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr23:23701816 G>A did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr23:23693152 G>C did not map to a codon.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr23:23693163 A>T did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr23:23693155 G>T did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr11:64085713 G>A maps to NM_012094.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr1:173455476 C>T maps to NM_004905.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:176731634 C>A maps to NM_013237.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:176731775 G>A maps to NM_013237.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr5:176733483 G>A maps to NM_013237.2 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr5:145176088 G>A maps to NM_182960.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr5:145197524 A>C maps to NM_182960.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:203453265 C>G maps to NM_201348.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:203452776 C>G maps to NM_201348.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr6:105821264 G>A maps to NM_002726.4 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr2:44549006 G>A maps to NM_001171603.1 Q685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr20:47248882 C>G maps to NM_020820.3 A1486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr20:47361600 C>T maps to NM_020820.3 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr20:47273600 G>A maps to NM_020820.3 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:47317391 G>A maps to NM_020820.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr8:69020479 C>G maps to NM_024870.2 S951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:69046487 C>T maps to NM_024870.2 Q1321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:69104736 C>T maps to NM_024870.2 I1527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr8:68931793 C>G maps to NM_024870.2 S75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr8:69030876 C>G maps to NM_024870.2 S1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr8:68950491 C>T maps to NM_024870.2 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr8:69030844 C>T maps to NM_024870.2 C1129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr8:68956793 G>C maps to NM_024870.2 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr8:69031742 C>T maps to NM_024870.2 F1166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr10:72358630 C>T maps to NM_005041.4 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr10:72360385 C>T maps to NM_005041.4 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr10:72358420 G>A maps to NM_005041.4 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr11:57156497 C>G maps to NM_002728.4 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:186276098 C>T maps to NM_005807.3 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:186280666 G>A maps to NM_005807.3 V1244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr1:186276419 A>G maps to NM_005807.3 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr20:62200823 G>A maps to NM_001037335.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:62195446 C>T maps to NM_001037335.2 L1576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr20:62200733 G>A maps to NM_001037335.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr20:62194405 G>A maps to NM_001037335.2 F1923F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr20:62198676 G>A maps to NM_001037335.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr20:62196283 G>A maps to NM_001037335.2 L1297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr20:62193081 C>T maps to NM_001037335.2 R2236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr20:62194087 G>A maps to NM_001037335.2 L2029L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:62198550 G>C maps to NM_001037335.2 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:62198715 G>C maps to NM_001037335.2 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr20:62198313 C>T maps to NM_001037335.2 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr20:62192536 G>A maps to NM_001037335.2 S2348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr20:62198523 G>A maps to NM_001037335.2 H729H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr20:62193647 G>A maps to NM_001037335.2 L2130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr20:62196493 G>A maps to NM_001037335.2 F1227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:42854113 C>A maps to NM_153026.2 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr12:42853913 G>T maps to NM_153026.2 Y731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr12:42866198 C>G maps to NM_153026.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:64084987 C>T maps to NM_198859.3 Q758Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:64148735 G>A maps to NM_198859.3 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr3:64184471 C>T maps to NM_198859.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr3:64132827 G>A maps to NM_198859.3 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:64132619 G>A maps to NM_198859.3 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:49040202 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr23:49040228 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr23:49040245 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr23:49040352 C>T did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr6:41753184 G>A maps to NM_013397.5 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:41753193 C>T maps to NM_013397.5 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:41753196 C>T maps to NM_013397.5 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:57183275 G>A maps to NM_000947.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr14:94187867 A>G maps to NM_178013.3 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr5:40769523 G>T maps to NM_206907.3 S212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:120118102 C>T maps to NM_006253.4 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr12:120106159 G>A maps to NM_006253.4 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:146639437 C>T maps to NM_005399.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr19:14208665 G>C maps to NM_002730.3 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr19:14204511 C>T maps to NM_002730.3 K286K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:14217607 C>A maps to NM_002730.3 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr19:14208238 G>T maps to NM_002730.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr19:14208577 G>A maps to NM_002730.3 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr19:14208662 C>A maps to NM_002730.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr19:14211651 C>T maps to NM_002730.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:84610101 C>T maps to NM_182948.2 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:49406882 G>C maps to NM_002733.3 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr7:151478310 G>C maps to NM_016203.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMJ-01A-11D-A42E-08 chr7:151483603 C>T maps to NM_016203.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr2:219688986 G>A maps to NM_017431.2 H437H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:66520183 C>G maps to NM_212472.1 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr17:66526541 C>G maps to NM_212472.1 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr7:647067 G>A maps to NM_002735.2 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:590101 G>A maps to NM_002735.2 Q371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:751070 C>A maps to NM_002735.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:48884886 G>C maps to NM_004157.2 S48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:64299088 C>A maps to NM_002737.2 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr17:64299004 G>A maps to NM_002737.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr17:64641534 C>T maps to NM_002737.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:64738853 G>A maps to NM_002737.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr17:64637549 C>G maps to NM_002737.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:24135199 G>A maps to NM_002738.6 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:24124315 G>T maps to NM_002738.6 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:53212458 C>T maps to NM_212539.1 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:53217514 T>C maps to NM_212539.1 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr3:53213623 G>A maps to NM_212539.1 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr3:53215505 G>A maps to NM_212539.1 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr3:53213614 G>A maps to NM_212539.1 Q46Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr3:53215526 C>T maps to NM_212539.1 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:53212464 C>T maps to NM_212539.1 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr2:46207513 C>T maps to NM_005400.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:46234715 C>T maps to NM_005400.2 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:46070184 C>G maps to NM_005400.2 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr19:54387460 C>T maps to NM_002739.3 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr19:54403696 C>T maps to NM_002739.3 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:54403678 C>T maps to NM_002739.3 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:54395051 G>A maps to NM_002739.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr19:54387437 C>T maps to NM_002739.3 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr14:61919977 G>A maps to NM_006255.3 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr14:61995798 G>C maps to NM_006255.3 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:169998122 C>T maps to NM_002740.5 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr10:6552957 C>T maps to NM_006257.2 W106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr10:6521007 G>T maps to NM_006257.2 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr10:6525399 A>T did not map to a codon.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr10:6553156 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr10:6539059 C>T maps to NM_006257.2 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr10:6484034 C>A maps to NM_006257.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:11558506 G>A did not map to a codon.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr1:2103574 C>T maps to NM_002744.4 N381N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr1:2082273 C>T maps to NM_002744.4 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr14:30046444 C>T maps to NM_002742.2 *913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr14:30100020 C>T maps to NM_002742.2 E533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr14:30098273 T>C maps to NM_002742.2 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr14:30105700 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr14:30068863 G>A maps to NM_002742.2 Q689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:47181773 C>T maps to ENST00000449438 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:47219558 G>A maps to ENST00000449438 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:47181743 G>A maps to ENST00000449438 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:47219390 C>T maps to ENST00000449438 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:47195049 G>A maps to ENST00000449438 V548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr19:47197162 G>A maps to ENST00000449438 D515D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr2:37494608 T>C maps to NM_005813.3 Q616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:37487527 C>G did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:37505008 C>G maps to NM_005813.3 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr8:48716042 T>C did not map to a codon.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr8:48846650 C>G did not map to a codon.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr8:48740848 C>T maps to NM_006904.6 E2818E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:48711930 C>T maps to NM_006904.6 Q3378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr8:48771463 C>T maps to NM_006904.6 L2096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr8:48740728 C>T maps to NM_006904.6 Q2858Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr8:48694763 A>G maps to NM_006904.6 L3815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr8:48803018 A>C maps to NM_006904.6 L1289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr8:48731992 G>A maps to NM_006904.6 Q3138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr8:48777245 G>A maps to NM_006904.6 F1813F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr8:48826511 G>A maps to NM_006904.6 F910F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr8:48809833 G>C maps to NM_006904.6 S1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr8:48801777 C>T maps to NM_006904.6 L1358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr8:48866214 G>T maps to NM_006904.6 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr8:48691019 C>T maps to NM_006904.6 Q3950Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr8:48746856 C>T maps to NM_006904.6 R2683R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr8:48734252 C>T maps to NM_006904.6 W3007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:82065387 C>T maps to NM_006259.1 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr4:82031654 G>A maps to NM_006259.1 F629F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr4:82126174 T>C maps to NM_006259.1 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr11:76072095 C>T maps to NM_004705.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:76063501 G>C maps to NM_004705.2 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:76066698 C>G did not map to a codon.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr11:76062029 A>G maps to NM_004705.2 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr11:76062360 G>A maps to NM_004705.2 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr11:76062189 C>A maps to NM_004705.2 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr11:76063815 T>C maps to NM_004705.2 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:3530356 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:3592643 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr23:3573362 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr6:22287783 G>C maps to ENST00000397199 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr2:238475308 G>A maps to NM_015893.1 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr10:120353727 G>A maps to NM_004248.2 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr10:120354300 G>T maps to NM_004248.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr10:120354618 G>T maps to NM_004248.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr5:35070328 G>C maps to NM_000949.4 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:11370221 G>A maps to ENST00000435245 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr16:11370005 G>A maps to ENST00000435245 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:50189925 G>A maps to NM_001536.3 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:148605048 C>T maps to NM_138364.2 Q30Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr4:148594916 C>T maps to NM_138364.2 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:148604988 G>A maps to NM_138364.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr4:148594961 G>A maps to NM_138364.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr21:48068368 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:23391414 G>A maps to NM_006109.3 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:107600218 G>A maps to NM_018137.2 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:107599528 C>T maps to NM_018137.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:107599528 C>T maps to NM_018137.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:107600311 G>A maps to NM_018137.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr16:68363000 G>A maps to NM_019023.2 K105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:128185987 G>A maps to ENST00000409048 E318E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:27038663 C>T maps to ENST00000415329 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr17:27031748 G>C maps to ENST00000415329 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:33764070 G>A maps to NM_006404.3 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr20:33762598 G>A maps to NM_006404.3 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr22:18918707 G>A maps to NM_016335.4 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr22:18918669 G>A maps to NM_016335.4 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr22:18905875 C>T maps to NM_016335.4 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr22:18905904 G>T maps to NM_016335.4 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:36303752 C>G maps to NM_021232.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:110993870 C>T maps to NM_032414.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr2:68882131 C>T maps to NM_138964.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr2:68882224 C>T maps to NM_138964.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr20:5282739 G>C maps to NM_144773.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr20:5283186 G>A maps to NM_144773.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr4:71275660 C>T maps to NM_021225.4 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr4:16010645 G>A maps to NM_006017.2 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr4:16020041 G>C maps to NM_006017.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:95940392 G>A maps to NM_144707.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:95940455 C>T maps to NM_144707.2 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr2:95950856 C>T maps to NM_144707.2 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr2:95954740 G>C maps to NM_144707.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:93605334 C>A maps to NM_000313.3 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:214169997 G>A maps to NM_002763.3 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr1:214170363 G>A maps to NM_002763.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr1:214185012 G>T maps to NM_002763.3 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr1:214170363 G>A maps to NM_002763.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr14:75329859 C>G maps to ENST00000445876 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr14:75330506 G>A maps to ENST00000445876 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr13:113814359 C>T maps to ENST00000342783 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr13:113825986 G>T maps to ENST00000342783 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr10:13655787 T>C maps to NM_003675.3 Y209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:13655814 G>A maps to NM_003675.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr10:13672267 G>A maps to NM_003675.3 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr11:60665570 A>C did not map to a codon.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:150307519 G>C maps to NM_004698.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:150307444 G>T maps to NM_004698.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr1:150325453 G>C maps to NM_004698.2 *684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:150300859 G>T maps to NM_004698.2 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:54628016 C>T maps to NM_015629.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:54627902 C>G maps to NM_015629.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr19:54625296 G>C maps to NM_015629.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr19:54627965 C>T maps to NM_015629.3 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:52874276 G>C maps to NM_032864.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:109241801 G>A maps to NM_018061.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr2:153537847 T>C maps to ENST00000410080 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr12:50029642 C>T maps to NM_001031698.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:50035704 C>T maps to NM_001031698.1 C572C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:50036433 C>T maps to NM_001031698.1 F676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr6:4058988 C>T maps to NM_003913.4 Q921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:4049305 C>G maps to NM_003913.4 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr20:62659060 C>T maps to NM_012469.3 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:62624834 C>G maps to NM_012469.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr20:62664344 G>A maps to NM_012469.3 *942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:1582370 G>A maps to NM_006445.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:1576683 G>T maps to NM_006445.3 T1208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:1579822 C>T maps to NM_006445.3 Q788Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr17:1579344 C>A maps to NM_006445.3 V852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr17:1562038 G>A maps to NM_006445.3 F1719F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:1564435 G>A maps to NM_006445.3 F1453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:1564633 G>A maps to NM_006445.3 F1423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:1557132 G>A maps to NM_006445.3 I2055I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr17:1582625 C>T maps to NM_006445.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:49689306 C>T maps to ENST00000451891 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr12:49690270 G>A maps to ENST00000451891 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr6:42689952 G>A maps to NM_000322.4 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr6:42672297 G>A maps to NM_000322.4 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:106871904 C>A did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:106893250 G>T did not map to a codon.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr23:106888520 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:106871962 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr7:18066916 C>T maps to NM_175886.2 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr7:18066661 C>T maps to NM_175886.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr23:12837719 G>T did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr23:12809711 G>C did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:74307741 G>A maps to NM_002766.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr17:18832197 C>A maps to NM_002767.2 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr17:18785971 C>T maps to NM_002767.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:57275119 G>A maps to NM_018304.3 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr17:57262919 G>A maps to NM_018304.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr17:57278990 G>A maps to NM_018304.3 *361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:57272756 G>A maps to NM_018304.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr19:50119180 C>T maps to NM_020719.1 L1734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr19:50123663 G>C maps to NM_020719.1 R1851R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr19:50102617 G>A maps to NM_020719.1 S1256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr19:50097788 C>A maps to NM_020719.1 S93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr16:30664039 A>T did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr16:30666442 C>G maps to NM_024031.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr5:120021827 C>A maps to NM_016644.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr2:240981280 G>A maps to NM_001080835.1 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:5783378 G>A maps to NM_001134316.1 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:138724387 C>T maps to NM_001134659.1 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:138724663 G>A maps to NM_001134659.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr3:138724642 G>A maps to NM_001134659.1 Y156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr3:138739002 C>A maps to NM_001013650.2 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr16:855663 C>T maps to NM_001013638.1 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr6:30530270 G>C maps to NM_025263.3 *189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr6:30529831 C>T maps to NM_025263.3 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr6:30529839 C>G maps to NM_025263.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr12:10999682 G>A maps to NM_007244.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr12:11000980 G>A maps to NM_007244.2 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr22:45132679 G>T maps to NM_001198721.1 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr22:45121153 C>T maps to ENST00000352766 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr22:45121150 C>T maps to ENST00000352766 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr22:45132763 G>A maps to NM_001198721.1 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr22:45182343 G>A maps to ENST00000352766 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr11:36422803 C>T maps to NM_001160167.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr11:36422826 C>A maps to NM_001160167.1 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr5:176882983 C>G maps to NM_001174101.1 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr5:126862373 C>T maps to ENST00000330542 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr23:37312441 A>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:37312429 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr23:150869179 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:150869282 G>T did not map to a codon.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr23:150869159 G>A did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr6:32118632 G>A maps to NM_030651.3 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr6:32117451 G>C maps to NM_030651.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr16:29825760 C>A maps to NM_145239.2 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr3:9989041 C>A maps to NM_207351.3 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr3:9989098 G>A maps to NM_207351.3 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:9988024 C>T maps to NM_207351.3 P944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:9991574 G>A maps to NM_207351.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr3:9989685 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:9989116 C>T maps to NM_207351.3 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:132484579 C>G maps to NM_016307.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr7:142459636 G>A maps to ENST00000486171 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr7:142460810 C>T maps to ENST00000486171 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr7:142460324 G>C maps to ENST00000486171 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr4:119216116 G>A maps to NM_003619.3 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr4:119256625 A>G did not map to a codon.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr4:119252872 G>A maps to NM_003619.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr4:119252890 G>A maps to NM_003619.3 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr6:27219021 C>A maps to NM_005865.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr6:27215721 C>A maps to NM_005865.3 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr7:142481237 G>C maps to ENST00000311757 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr7:142481258 C>T maps to ENST00000311757 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr7:142481246 C>T maps to ENST00000311757 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:2868795 C>T maps to NM_006799.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr16:2871482 C>T maps to NM_006799.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr16:2871500 G>A maps to NM_006799.2 W280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:86518960 C>T maps to NM_007173.4 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr16:2762752 G>A maps to NM_031948.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr9:33797838 G>A maps to NM_007343.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:2835104 G>A maps to NM_152891.2 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr16:2835819 T>A maps to NM_152891.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr6:84233294 C>T maps to NM_153362.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:84233552 C>T maps to NM_153362.2 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:31157214 G>A maps to NM_173502.3 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr16:31159962 C>G maps to NM_173502.3 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr1:228005155 G>A maps to NM_183062.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:46874528 G>C maps to NM_182702.1 S180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr16:58320014 G>A maps to NM_001080492.1 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:58314502 G>A maps to NM_001080492.1 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:58319876 C>T maps to NM_001080492.1 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr16:31144159 G>C maps to NM_002773.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr16:31144120 G>A maps to NM_002773.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:31144246 G>C maps to NM_002773.3 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr16:31143398 C>T maps to NM_002773.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr10:25226220 T>A maps to NM_020200.5 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr15:55970093 C>A maps to NM_173814.4 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr15:55964652 G>A maps to NM_173814.4 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr15:55919292 G>C maps to NM_173814.4 S947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr19:843530 C>T maps to NM_002777.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:150981119 C>G maps to NM_021222.1 Y4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr1:151001263 C>T maps to NM_021222.1 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:151006325 G>A maps to NM_021222.1 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr9:79323648 C>A maps to NM_015225.2 E1181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr9:79320826 G>A maps to NM_015225.2 L2121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:79318820 C>A maps to NM_015225.2 E2570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:79321291 G>T maps to NM_015225.2 V1966V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr9:79267411 C>T maps to NM_015225.2 E2848E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr9:79318836 C>T maps to NM_015225.2 E2564E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr9:79441571 C>G maps to NM_015225.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr9:79324196 G>C maps to NM_015225.2 S998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr9:79323131 G>T maps to NM_015225.2 S1353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr9:79318701 G>C maps to NM_015225.2 L2609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr19:40909763 C>T maps to NM_181882.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr19:40909667 G>A maps to NM_181882.2 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:40902868 G>A maps to NM_181882.2 R464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr19:40901222 G>A maps to NM_181882.2 A1012A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr19:40903790 G>A maps to NM_181882.2 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr19:40902542 C>T maps to NM_181882.2 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:40901225 C>T maps to NM_181882.2 G1011G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:40902006 G>C maps to NM_181882.2 S751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:40901698 G>A maps to NM_181882.2 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr19:40909733 C>T maps to NM_181882.2 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr19:40901510 C>A maps to NM_181882.2 G916G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr19:40900286 C>T maps to NM_181882.2 E1324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr10:73587833 G>A maps to ENST00000373120 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:80912184 C>G maps to ENST00000421149 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr9:80919827 C>T maps to ENST00000421149 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr9:80943902 G>T maps to ENST00000421149 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr9:80921228 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:143762796 C>T maps to ENST00000301258 C35C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr8:143763435 C>A maps to ENST00000301258 C86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:104173860 G>A maps to NM_002779.3 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr10:104174908 G>A maps to NM_002779.3 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr10:104170614 C>T maps to NM_002779.3 K697K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr10:104165235 G>A maps to NM_002779.3 V731V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr5:139193133 G>A maps to NM_032289.2 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr5:139221899 C>T maps to NM_032289.2 I719I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr5:139193895 C>G maps to NM_032289.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr8:18623023 G>A maps to ENST00000440756 Q705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:18622976 G>A maps to ENST00000440756 F720F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr8:18393455 C>A maps to ENST00000440756 E983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr8:18413805 G>A maps to ENST00000440756 A949A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr2:113940992 C>T maps to NM_012455.2 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:113940802 C>G maps to NM_012455.2 S257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr14:73673091 A>C did not map to a codon.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr14:73640329 C>G maps to NM_000021.3 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:227071518 G>A maps to ENST00000391872 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:227071518 G>A maps to ENST00000391872 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr19:36237636 C>G maps to NM_172341.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr19:43376147 C>T maps to NM_006905.2 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr19:43372232 C>G maps to NM_006905.2 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:43382063 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:43382131 G>A maps to NM_006905.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr19:43372458 G>T maps to NM_006905.2 S346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr19:43373184 C>T maps to NM_006905.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:43575861 G>C maps to NM_031246.3 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:43575869 A>G maps to NM_031246.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr19:43579764 G>A maps to NM_031246.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr19:43576075 G>C maps to NM_031246.3 S247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:43585207 G>A maps to ENST00000449000 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr19:43234014 C>G maps to NM_021016.3 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr19:43236984 C>T maps to NM_021016.3 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr19:43233960 G>T maps to NM_021016.3 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr19:43233344 G>A maps to NM_021016.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr19:43708310 G>A maps to NM_002780.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr19:43698637 C>T maps to NM_002780.3 W366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr19:43708146 C>A maps to NM_002780.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:43680124 G>A maps to ENST00000270059 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:43690518 G>T maps to ENST00000270059 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:43421932 G>A maps to NM_002782.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr19:43411740 G>A maps to NM_002782.3 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:43441168 G>A maps to NM_002783.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:43428960 C>T maps to NM_002783.2 *420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:43430590 G>A maps to NM_002783.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr19:43428960 C>T maps to NM_002783.2 *420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr19:43430050 G>A maps to NM_002783.2 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr19:43259416 C>T maps to NM_182707.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr19:43763020 G>A maps to NM_002784.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr19:43757761 C>G maps to NM_002784.3 *427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:43762546 G>A maps to NM_002784.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr9:15466853 G>C maps to NM_001128217.1 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr9:15468841 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr9:15472666 G>A maps to NM_001128217.1 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:15506557 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr9:15486844 C>A maps to NM_001128217.1 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr9:15489993 G>C maps to NM_001128217.1 S93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr9:15474227 C>A maps to NM_001128217.1 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr9:15468625 A>G did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr9:15490122 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr9:15510156 G>A maps to NM_001128217.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr16:67942807 C>T maps to NM_006742.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr16:67942657 C>G maps to NM_006742.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:67961248 C>T maps to NM_006742.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:87076267 G>A maps to ENST00000276616 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr8:87076676 G>T maps to ENST00000276616 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr8:87076598 G>A maps to ENST00000276616 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:42964296 C>T maps to NM_002787.4 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr7:42964278 C>T maps to NM_002787.4 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr7:42964311 C>T maps to NM_002787.4 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr15:78841183 C>G maps to NM_002789.4 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr15:78834985 G>T maps to NM_002789.4 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr20:60712443 G>A maps to NM_002792.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr20:60714932 G>A maps to NM_002792.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr18:23724561 G>T maps to NM_144662.2 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:67970131 G>A maps to NM_002801.2 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr16:67970131 G>A maps to NM_002801.2 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:67969551 C>G maps to NM_002801.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr14:23511539 C>T maps to NM_001099780.1 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr17:36909446 G>A maps to NM_002795.2 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:151373007 G>A maps to NM_002796.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr9:127115945 G>A maps to NM_002799.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:32808758 G>A maps to NM_148919.3 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr6:32810815 C>T maps to NM_148919.3 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr6:32826142 A>G maps to NM_002800.4 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr7:102988223 C>T maps to NM_002803.2 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr7:103003798 G>A maps to NM_002803.2 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr7:103007920 G>C maps to NM_002803.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr7:103008416 G>A maps to NM_002803.2 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:40480724 T>C maps to NM_006503.2 H221H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr19:40480225 G>C maps to NM_006503.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr19:40486587 G>A maps to NM_006503.2 K369K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr17:61908423 C>A maps to NM_002805.5 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr17:61908477 C>T maps to NM_002805.5 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:61908761 G>T maps to NM_002805.5 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr14:53173936 C>A maps to NM_002806.3 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr14:53177835 G>A maps to NM_002806.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:231936986 C>T maps to NM_002807.3 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr2:231947595 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr23:107331993 A>G did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:107331015 T>C did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:30807592 C>T maps to NM_002815.2 Q405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr17:30796164 C>T maps to NM_002815.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr17:65340840 C>A maps to NM_002816.3 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr17:65353673 G>A maps to NM_002816.3 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr17:65340790 C>A maps to NM_002816.3 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr3:184026527 G>A maps to NM_002808.3 P859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:184019341 C>T maps to NM_002808.3 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:184019709 C>A maps to NM_002808.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:184019841 C>T maps to NM_002808.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr3:184021745 T>C maps to NM_002808.3 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr3:184026674 C>G maps to NM_002808.3 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:38140721 C>T maps to NM_002809.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:38151283 C>G maps to NM_002809.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:38151528 G>A maps to NM_002809.2 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:151239817 G>T maps to ENST00000368881 *381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:151239668 G>C maps to ENST00000368881 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr3:64008134 G>C maps to ENST00000492933 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:64004502 G>C maps to ENST00000492933 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr16:74330811 G>A did not map to a codon.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr19:38865492 G>T maps to NM_002812.4 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr12:122337705 C>T maps to NM_002813.4 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr14:24606975 G>A maps to NM_176783.1 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr14:24614966 G>C maps to ENST00000429021 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr2:54093285 G>A maps to NM_014614.2 F1824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr2:54159083 G>A maps to NM_014614.2 Q402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr2:54167097 G>A maps to NM_014614.2 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr2:54133981 G>A maps to NM_014614.2 I936I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:54148028 G>T maps to NM_014614.2 I753I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr20:1099529 G>A maps to NM_006814.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr21:40547516 C>G maps to NM_003720.2 *289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr18:12725499 T>C maps to NM_020232.4 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr18:12706693 C>G maps to NM_020232.4 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr7:1608852 C>T maps to NM_001134340.1 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr6:31107474 G>A maps to NM_014068.2 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:31106439 G>A maps to NM_014068.2 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:31106553 C>T maps to NM_014068.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr6:31105958 G>C maps to NM_014069.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr13:20277421 G>A maps to NM_001042414.1 Q489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr7:56079508 G>A maps to NM_004577.3 N208N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr7:56088884 C>G maps to NM_004577.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr7:56085002 A>G maps to NM_004577.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr10:124742269 C>T maps to NM_153336.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr10:124740003 C>T maps to NM_153336.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr10:124740054 C>G maps to NM_153336.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr15:77323594 C>T maps to NM_003978.3 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr15:77324700 C>T maps to NM_003978.3 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:28477481 G>C maps to NM_001164721.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:28477355 G>A maps to NM_001164721.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:28476797 G>A maps to NM_001164721.1 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:28477481 G>T maps to NM_001164721.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:28477334 G>A maps to NM_001164721.1 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:72333392 C>A maps to NM_001099666.1 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr19:808705 C>T maps to NM_002819.4 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr19:804123 C>T maps to NM_002819.4 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:99021514 C>A maps to NM_001198879.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr7:99032711 G>A maps to NM_001198879.1 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr7:99032853 C>G maps to NM_001198879.1 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr7:99021496 G>A maps to NM_001198879.1 I656I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr5:71616251 C>T maps to NM_024754.3 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:86364194 C>T maps to NM_017952.5 F637F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr9:98221996 C>A maps to NM_000264.3 T924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:98211362 G>A maps to NM_000264.3 F1264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:45293263 C>G maps to NM_003738.4 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:45295678 C>G maps to NM_003738.4 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:45293232 C>A maps to NM_003738.4 E738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr23:23398218 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr23:23412193 G>C did not map to a codon.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr23:23398358 G>A did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:23411546 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr23:23411276 T>A did not map to a codon.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr23:23411318 G>T did not map to a codon.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr23:23353216 G>A did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:23353088 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:23411412 A>G did not map to a codon.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:11561645 G>C maps to NM_020780.1 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr1:11596719 C>T maps to NM_020780.1 L1386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr1:11561855 G>A maps to NM_020780.1 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr1:11596631 C>T maps to NM_020780.1 F1356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:11596694 C>A maps to NM_020780.1 L1377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr1:11561105 G>A maps to NM_020780.1 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr1:11574557 G>A maps to NM_020780.1 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:11561726 G>C maps to NM_020780.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:11576121 G>A maps to NM_020780.1 Q551Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:11589877 C>T maps to NM_020780.1 F988F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr10:27703134 C>T maps to NM_001034842.3 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:27702464 G>A maps to NM_001034842.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr10:27702831 G>T maps to NM_001034842.3 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr10:27688158 G>A maps to NM_001034842.3 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr10:27702330 G>A maps to NM_001034842.3 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr6:42893344 C>G maps to NM_138296.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr6:42883833 C>T maps to NM_138296.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr6:42890771 C>T maps to NM_138296.2 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:97321823 C>T maps to NM_014754.1 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr10:89624274 C>T maps to NM_000314.4 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr10:89725042 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr10:89717707 C>T maps to NM_000314.4 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr10:89717614 C>T maps to NM_000314.4 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr10:89711912 T>G maps to NM_000314.4 Y177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr10:89720740 C>T maps to NM_000314.4 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr10:89624274 C>T maps to NM_000314.4 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr14:52741531 A>G maps to NM_000953.2 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr9:139873473 C>T maps to ENST00000224167 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr14:52781490 G>A maps to NM_000956.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr14:52781367 C>T maps to NM_000956.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr14:52781832 C>T maps to NM_000956.3 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr14:52781414 G>A maps to NM_000956.3 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:71512495 G>C maps to ENST00000354608 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr5:40681892 C>G maps to NM_000958.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:40692209 C>G maps to NM_000958.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr5:40681628 G>A maps to NM_000958.2 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr9:130887693 C>T maps to NM_025072.5 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr9:130883528 C>T maps to NM_025072.5 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr12:57064085 G>A maps to NM_006601.5 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr1:78958973 G>A maps to NM_000959.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr1:78958965 C>T maps to NM_000959.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:79002358 C>A maps to NM_000959.3 S356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:117529498 C>T maps to NM_020440.2 I850I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:117509835 C>G maps to NM_020440.2 S648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr19:47124611 G>A maps to NM_000960.3 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr20:48130896 G>C maps to NM_000961.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr20:48129667 G>T maps to NM_000961.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr20:48129775 G>C maps to NM_000961.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr9:125140274 C>T maps to NM_000962.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr1:186646839 G>A maps to NM_000963.2 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:186645812 G>C maps to NM_000963.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr1:186646843 C>T maps to NM_000963.2 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr3:46945129 G>A maps to NM_000316.2 W589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr3:46943272 C>T maps to NM_000316.2 F378F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-GD-A3OP-01A-21D-A21Z-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr19:49925823 G>A maps to NM_178449.3 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr2:209292999 C>G maps to NM_005048.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr2:209309550 C>G maps to NM_005048.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr2:209358260 C>T maps to NM_005048.2 H510H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr12:28122373 G>A maps to ENST00000354417 Y18Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr12:28116291 C>T maps to ENST00000354417 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr12:28116417 C>T maps to ENST00000354417 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:141810663 C>A maps to NM_005607.4 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr8:141889681 C>A maps to NM_005607.4 G106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr8:27255124 G>A maps to NM_004103.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr8:27294952 G>A maps to NM_004103.3 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr20:62162260 C>T maps to NM_005975.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr20:62166351 G>A maps to NM_005975.2 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr20:62162155 G>A maps to NM_005975.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:62165582 G>A maps to NM_005975.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr20:62162197 C>T maps to NM_005975.2 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:43114420 C>T maps to NM_002821.3 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr6:43096925 C>T maps to NM_002821.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr6:43109404 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr12:6878819 C>A maps to NM_002824.4 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr12:6879606 G>C maps to NM_002824.4 *103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr7:136935979 G>A maps to NM_002825.5 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FM-01A-11D-A38G-08 chr19:50357742 C>T maps to NM_017432.3 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:50361876 G>A maps to NM_017432.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr19:50360993 C>G maps to NM_017432.3 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr19:50360311 C>T maps to NM_017432.3 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr1:32374485 G>A maps to NM_080391.3 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr8:142437046 G>A maps to NM_032611.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr8:142441036 G>T maps to NM_032611.1 G139*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BT-A0YX-01A-11D-A10S-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr9:96846859 C>T maps to ENST00000434261 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr9:96847647 G>A maps to ENST00000434261 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr10:17645946 C>T maps to NM_014241.3 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:65847288 G>A maps to NM_016395.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr15:65849118 C>T maps to NM_016395.2 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:65862541 G>C did not map to a codon.
Sequencing variant TCGA-CF-A9FH-01A-11D-A38G-08 chr9:21011605 A>G maps to NM_001010915.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr9:21015925 G>A maps to NM_001010915.3 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr11:47591331 G>A maps to NM_175732.2 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr20:49191064 A>G maps to NM_002827.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr20:49196246 G>A maps to NM_002827.2 W291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr7:77200496 C>T maps to NM_002835.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr7:77256768 C>T maps to NM_002835.3 F591F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr7:77256780 C>T maps to NM_002835.3 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:77256780 C>T maps to NM_002835.3 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr4:87672040 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr4:87691108 A>G maps to NM_080685.2 G1564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:87653920 T>C did not map to a codon.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr4:87694008 G>A maps to NM_080685.2 S1754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:87685792 T>G maps to NM_080685.2 T1355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr4:87671650 C>T maps to NM_080685.2 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:87671722 C>T maps to NM_080685.2 L917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr4:87696774 C>A maps to NM_080685.2 S1959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr4:87726517 T>G maps to NM_080685.2 L2252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr4:87735665 G>T maps to NM_080685.2 E2479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr4:87703404 C>A maps to NM_080685.2 S2010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr1:214568274 G>A maps to NM_005401.4 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr1:214537995 C>T maps to NM_005401.4 S1098S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:214551304 C>T maps to NM_005401.4 E895E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:214542944 C>T maps to NM_005401.4 T1042T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr1:214546152 G>A maps to NM_005401.4 Y979Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr2:131127378 C>T maps to NM_014369.3 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr18:12794330 A>T maps to NM_002828.2 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr18:12794398 C>A maps to NM_002828.2 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr14:88938709 G>A maps to NM_007039.3 R917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr14:88945818 G>C maps to NM_007039.3 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr14:88974365 T>C did not map to a codon.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr14:88983602 G>A maps to NM_007039.3 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr14:88983465 G>T maps to NM_007039.3 S107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr14:88934486 G>C maps to NM_007039.3 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr14:88945860 G>A maps to NM_007039.3 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr1:114380650 C>T maps to NM_015967.5 Q457Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr1:114380500 G>A maps to NM_015967.5 H507H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:114380650 C>T maps to NM_015967.5 Q457Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr1:114380325 G>A maps to NM_015967.5 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:114401971 A>G did not map to a codon.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr1:114401986 C>T maps to NM_015967.5 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr3:47447451 C>T maps to NM_015466.2 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr9:112216855 T>A did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr9:112225591 C>T maps to NM_002829.3 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr9:112151538 A>G maps to NM_002829.3 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr9:112189305 G>A maps to NM_002829.3 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:112153420 C>T maps to NM_002829.3 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:112190911 G>A maps to NM_002829.3 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr9:112145728 G>A maps to NM_002829.3 R786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:112144706 C>T maps to NM_002829.3 V801V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr9:112182794 C>A maps to NM_002829.3 E408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr9:112182795 C>A maps to NM_002829.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:120725490 T>C maps to NM_002830.2 Y879Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr11:18751344 G>A maps to NM_032781.3 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:7064629 C>T maps to ENST00000416215 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr12:7060781 C>T maps to ENST00000416215 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:202124737 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr1:202123439 C>T maps to ENST00000309017 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr15:75798200 G>A maps to NM_002833.2 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr15:75798061 C>A maps to NM_002833.2 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr15:75809617 T>C maps to NM_002833.2 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr20:3007824 G>A maps to NM_002836.3 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:2968990 G>A maps to NM_002836.3 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr20:3008456 G>C maps to NM_002836.3 V630V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr12:70970177 G>A maps to NM_001109754.1 F942F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:70932749 G>C maps to NM_001109754.1 L1941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr12:70938415 G>C maps to NM_001109754.1 L1805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:70949009 G>A maps to NM_001109754.1 V1691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr12:71016175 A>G maps to NM_001109754.1 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr12:70960367 C>A maps to NM_001109754.1 E1251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr12:70988421 C>T maps to NM_001109754.1 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:70928395 G>A maps to NM_001109754.1 H2080H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:198701484 C>T maps to ENST00000271610 N677N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:198711036 C>T maps to ENST00000271610 Q815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:198723442 C>G maps to ENST00000271610 L1185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:198713181 G>T did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:198672486 C>G maps to ENST00000271610 S215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr1:198678921 C>T maps to ENST00000271610 N380N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:198711116 C>T maps to ENST00000271610 F841F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr1:198721820 C>T maps to ENST00000271610 V1143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:198697494 C>T maps to ENST00000271610 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr11:67203344 G>A maps to NM_005608.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr9:8521490 T>A maps to NM_002839.3 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr9:8484312 G>A maps to NM_002839.3 V1073V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:8485768 C>A maps to NM_002839.3 V1016V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr9:8518313 T>C maps to NM_002839.3 K359K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr9:8518001 G>A maps to NM_002839.3 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr9:8517967 G>A maps to NM_002839.3 Q475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr10:129871677 C>T maps to NM_006504.4 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr10:129839165 C>T maps to NM_006504.4 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr1:44085039 C>T maps to NM_002840.3 I1576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:44072609 C>G maps to NM_002840.3 L1276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr1:44086231 C>T maps to NM_002840.3 F1782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:44072573 G>A maps to NM_002840.3 V1264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:44083219 C>T maps to NM_002840.3 V1392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr1:44086651 G>A maps to NM_002840.3 T1836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:62261594 G>A maps to NM_002841.3 Q1171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:62188854 G>A maps to NM_002841.3 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:62254771 G>A maps to NM_002841.3 T979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr3:61547999 C>T maps to NM_002841.3 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr3:62189367 T>A maps to NM_002841.3 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr3:61989041 C>T maps to NM_002841.3 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr19:55697685 G>T maps to NM_002842.3 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:55693229 G>C maps to NM_002842.3 L1080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr19:55693509 C>T maps to NM_002842.3 V1024V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr19:55703083 G>A maps to NM_002842.3 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:55713438 G>A maps to NM_002842.3 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:48185098 C>T maps to NM_002843.3 I1216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:48161323 C>T maps to NM_002843.3 I813I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr11:48149392 C>A maps to NM_002843.3 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:48152047 C>T maps to NM_002843.3 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr11:48188772 C>T maps to NM_002843.3 L1291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr11:48145333 G>A maps to NM_002843.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:128410864 C>A maps to ENST00000368210 E479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr6:128410868 C>T maps to ENST00000368210 E477E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr6:128294302 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr18:7888248 C>T maps to NM_001105244.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr18:8143717 C>T maps to NM_001105244.1 I747I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr18:7926629 C>T maps to NM_001105244.1 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr18:8069869 C>G maps to NM_001105244.1 S440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:220166949 G>A maps to NM_002846.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:220172523 G>A maps to NM_002846.3 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr7:157361642 C>G maps to NM_002847.3 R951R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr7:157369411 C>T maps to NM_002847.3 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr7:157926661 G>C maps to NM_002847.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:157341672 C>T maps to NM_002847.3 L981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr7:157361642 C>G maps to NM_002847.3 R951R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr7:157926406 G>A maps to NM_002847.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr7:157361624 C>T maps to NM_002847.3 L957L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr7:157874044 G>A maps to NM_002847.3 F556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr7:157370772 G>A maps to NM_002847.3 G852G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr12:15668438 C>G maps to NM_030667.1 S491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr12:15656840 G>C did not map to a codon.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr12:15747917 G>A maps to NM_030667.1 K1198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:15475708 C>T maps to NM_030667.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr12:71139707 C>A maps to NM_002849.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr12:71056364 C>A maps to NM_002849.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr12:71286461 C>A maps to NM_002849.2 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr12:71286578 C>T maps to NM_002849.2 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr12:71148003 G>C maps to NM_002849.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:5231462 C>T maps to NM_002850.3 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr19:5244215 G>A maps to NM_002850.3 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr19:5212394 G>A maps to NM_002850.3 V1574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:5222810 G>A maps to NM_002850.3 Q998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr19:5210809 C>T maps to NM_002850.3 Q1747Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:5245928 G>A maps to NM_002850.3 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:5211776 C>T maps to NM_002850.3 R1686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr20:40980877 C>T maps to ENST00000373198 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr20:41100918 C>T maps to ENST00000373198 Q479Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr20:40864898 C>A did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr20:40757391 A>G did not map to a codon.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr20:41514513 G>T maps to ENST00000373198 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr20:40748573 C>T did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr20:41385231 G>C maps to ENST00000373198 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr20:40730769 C>T maps to ENST00000373198 L1258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr20:41419867 G>C maps to ENST00000373198 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr20:40980871 C>T maps to ENST00000373198 Q538Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr1:29585260 C>T maps to NM_005704.4 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:29647255 C>G maps to NM_005704.4 P1259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:121671534 C>T maps to NM_002851.2 V1696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr7:121650920 T>C maps to NM_002851.2 Y607Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr7:121674147 G>C did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr7:121652138 G>A maps to NM_002851.2 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr7:121652342 G>A maps to NM_002851.2 L1081L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr7:121699833 C>T maps to NM_002851.2 F2233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:121653265 C>G maps to NM_002851.2 S1389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr7:121676717 C>T maps to NM_002851.2 I1783I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr17:40556938 G>A maps to NM_012232.5 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr17:40574809 G>A maps to NM_012232.5 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr11:112104238 C>T maps to NM_000317.2 Y133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr21:46275170 C>G maps to NM_004339.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr21:46285353 G>A maps to NM_004339.2 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:157160548 G>A maps to NM_002852.3 Q309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr3:157160218 G>A maps to NM_002852.3 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr16:1536305 G>A maps to NM_001013658.1 D352D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr16:1535987 G>A maps to NM_001013658.1 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:1536455 G>A maps to NM_001013658.1 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr16:1536185 G>A maps to NM_001013658.1 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr16:1537950 C>G maps to NM_001013658.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr16:1535940 C>G maps to NM_001013658.1 *474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr8:144899770 G>A maps to NM_078480.1 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr8:144899902 G>C maps to NM_078480.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:144898722 C>T maps to NM_078480.1 Q549Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr8:144900578 G>A maps to NM_078480.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:31437554 G>A maps to ENST00000373741 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr1:31478698 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:31532157 G>A maps to ENST00000373741 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr1:31439029 G>A maps to ENST00000373741 Q665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:31465282 G>C maps to ENST00000373741 S407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:31532157 G>A maps to ENST00000373741 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:31465319 G>A maps to ENST00000373741 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:31478735 T>C maps to ENST00000373741 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:20451399 C>T maps to ENST00000361078 L1049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr2:20455915 C>A maps to ENST00000361078 E836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr2:20455895 G>C maps to ENST00000361078 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:20507823 C>T maps to ENST00000361078 Q266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr5:139494614 G>A maps to NM_005859.4 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr5:139494116 C>T maps to NM_005859.4 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr5:139494275 C>T maps to NM_005859.4 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr5:139494638 C>G maps to NM_005859.4 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr5:139494678 G>T maps to NM_005859.4 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr7:44924287 C>T maps to NM_033224.3 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr8:30889362 C>T maps to NM_013357.2 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr8:30889905 C>T maps to NM_013357.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr8:30889905 C>G maps to NM_013357.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:132426503 C>A maps to NM_025215.5 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:132426134 G>C maps to NM_025215.5 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:132426464 G>C maps to NM_025215.5 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr12:132425975 G>T maps to NM_025215.5 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:61175206 G>A maps to NM_144709.2 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr11:125765329 G>A maps to NM_031307.3 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr11:125764063 A>G maps to NM_031307.3 N354N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr7:105111174 G>C maps to NM_019042.3 S453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:105142963 G>A maps to NM_019042.3 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr7:105112640 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr12:44148850 A>G maps to NM_031292.3 N66N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr12:44124322 T>C maps to NM_031292.3 Q654Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr12:44142293 G>A maps to NM_031292.3 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr1:1245096 G>A maps to NM_153339.1 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:1244650 C>T maps to NM_153339.1 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:1246356 G>A maps to NM_153339.1 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:1246025 C>T maps to NM_153339.1 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:99818726 C>T maps to NM_024070.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr11:119547810 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:119545905 G>A maps to NM_002855.4 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr11:119549199 C>A maps to NM_002855.4 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr11:119599209 G>A maps to NM_002855.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr19:45375389 G>A maps to NM_001042724.1 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr19:45375179 C>A maps to NM_001042724.1 C183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr19:45368627 G>A maps to NM_001042724.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr3:110845148 C>T maps to NM_015480.1 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:110837614 C>T maps to NM_015480.1 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:161044086 G>C maps to NM_030916.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:161043068 C>T maps to NM_030916.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr1:161049708 G>C maps to NM_030916.2 S37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:161046191 G>C maps to NM_030916.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:161043041 G>C maps to NM_030916.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr21:45548230 C>T maps to NM_005049.2 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr21:45542226 G>A maps to NM_005049.2 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr21:45548014 G>A maps to NM_005049.2 A781A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr21:45547981 C>T maps to NM_005049.2 N770N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr5:159546011 C>T maps to NM_001130864.1 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr5:159507712 C>T maps to NM_052927.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr5:159520822 G>A maps to NM_001130864.1 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr10:134218732 G>C maps to NM_138499.3 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr2:1652230 C>A maps to NM_012293.1 R1107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:1643177 C>T maps to NM_012293.1 G1323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr2:1647242 C>A maps to NM_012293.1 R1283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:1639254 G>A maps to NM_012293.1 C1415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr2:1667491 C>A maps to NM_012293.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr2:1638071 C>A maps to NM_012293.1 V1448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr2:1652947 C>T maps to NM_012293.1 R868R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr2:1680816 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr2:1652719 G>A maps to NM_012293.1 S944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:1652203 C>A maps to NM_012293.1 P1116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr8:52321369 T>C maps to NM_144651.4 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr8:52320895 C>A maps to NM_144651.4 G1096G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr8:52321347 G>A maps to NM_144651.4 R946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr8:52287281 G>A maps to NM_144651.4 G1189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr8:52321798 G>A maps to NM_144651.4 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr8:52366133 A>T maps to NM_144651.4 C398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr8:52284498 G>A maps to NM_144651.4 Q1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:58377552 C>T maps to NM_017771.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:58382890 C>T maps to NM_017771.3 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:133277848 C>A maps to NM_018663.1 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:133281206 C>T maps to NM_018663.1 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr20:32295583 G>C maps to NM_007238.4 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr16:31212906 C>T maps to NM_013258.4 *196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr16:31213925 G>T maps to NM_013258.4 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:79893380 C>T maps to ENST00000432920 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr17:79891090 C>G maps to ENST00000432920 *347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr17:79891200 C>T maps to ENST00000432920 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr17:79891179 C>T maps to ENST00000432920 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:226109032 T>A maps to NM_013328.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr16:31228190 G>A maps to NM_152901.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr16:31228166 G>C maps to NM_152901.2 Y61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr20:25261744 C>A maps to NM_002862.3 S467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr20:25262737 G>A maps to NM_002862.3 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr20:25229005 C>T maps to NM_002862.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr20:25264855 C>G maps to NM_002862.3 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr20:25263870 C>T maps to NM_002862.3 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:25271211 G>A maps to NM_002862.3 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr20:25259721 C>A maps to NM_002862.3 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr20:25273201 C>T maps to NM_002862.3 F710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr20:25249782 G>T maps to NM_002862.3 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr20:25228819 G>A maps to NM_002862.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr14:51378472 G>A maps to NM_002863.4 N648N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr14:51378883 C>T maps to NM_002863.4 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr11:64522182 G>A maps to NM_005609.2 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr11:64518842 G>C maps to NM_005609.2 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr11:64525783 G>A maps to NM_005609.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:64518836 G>A maps to NM_005609.2 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr11:64525361 C>T maps to NM_005609.2 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:64514250 G>A maps to NM_005609.2 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr15:55839114 G>T maps to NM_015617.1 Y122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:158911861 A>G maps to NM_152501.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:158906856 G>T maps to NM_152501.3 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr1:158912083 G>A maps to NM_152501.3 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:158912101 C>T maps to NM_152501.3 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr12:21608983 G>A maps to NM_024854.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:100174796 C>T maps to NM_032709.2 K32K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:9321514 G>C maps to NM_002864.2 S686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:9349178 C>A maps to NM_002864.2 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:9356465 C>T maps to NM_002864.2 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr12:9334657 T>C maps to NM_002864.2 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:9346774 C>G maps to NM_002864.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:9305843 C>T maps to NM_002864.2 Q1290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr20:3147629 C>T maps to NM_014731.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr20:3146670 A>C maps to NM_014731.2 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr20:3145258 C>G maps to NM_014731.2 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr3:49139106 G>T maps to NM_005051.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr3:49137691 G>C maps to NM_005051.1 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr3:49135632 G>A maps to NM_005051.1 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr3:49136833 G>A maps to NM_005051.1 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr3:49136323 G>A maps to NM_005051.1 F619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:49138029 G>A maps to NM_005051.1 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr6:163984653 C>T maps to ENST00000361752 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr6:163984776 A>G maps to NM_206855.2 *320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr6:163983039 G>A maps to ENST00000361752 K197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr6:163899809 A>C did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr2:37586816 C>G maps to NM_012413.3 S121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:37586826 C>T maps to NM_012413.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr4:122254085 C>T maps to NM_198179.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:49081853 C>T maps to NM_198880.1 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr17:74300989 C>T maps to NM_032134.1 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr17:74283885 G>A maps to NM_032134.1 V1131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr17:74277001 G>A maps to NM_032134.1 A1266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:74287645 A>C maps to NM_032134.1 P888P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr17:74288235 G>A maps to NM_032134.1 Q692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr17:74288281 G>T maps to NM_032134.1 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr6:107113689 C>G maps to NM_018292.4 S467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr6:107096957 C>T maps to NM_018292.4 Q147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr6:107110890 G>A maps to NM_018292.4 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr11:32955869 A>G maps to NM_001076786.1 S893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr11:32997930 C>T maps to NM_001076786.1 Q1707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:32954970 G>T maps to NM_001076786.1 E594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr11:32949664 G>A maps to NM_001076786.1 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:32955537 C>T maps to NM_001076786.1 Q783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr11:32975401 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr1:180158778 C>T maps to NM_002826.4 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:180166063 C>T maps to NM_002826.4 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr19:10823912 C>T maps to NM_031209.2 D393D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr19:10822942 G>A maps to NM_031209.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr2:136481759 G>A maps to ENST00000409606 Q1067Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr2:136396629 C>G maps to ENST00000409606 S386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr2:136396464 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:136362420 G>A maps to ENST00000409606 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr20:42969879 C>T maps to NM_178491.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:66172007 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr19:8467367 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr8:37732220 C>G maps to NM_001002814.2 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:37728858 G>T maps to NM_001002814.2 S1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr8:37730039 C>A maps to NM_001002814.2 V760V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr8:37734861 G>A maps to NM_001002814.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:119799771 G>A maps to ENST00000369199 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr10:119799754 C>A maps to ENST00000369199 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr10:119799715 A>G maps to ENST00000369199 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr16:569851 G>A maps to NM_014700.3 E607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:29848999 C>T maps to NM_032932.3 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:29855789 C>G maps to NM_032932.3 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr17:29848182 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr2:73315527 C>G maps to NM_015470.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr2:73315527 C>G maps to NM_015470.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:73339500 G>A maps to NM_015470.2 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:73339599 G>A maps to NM_015470.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr18:8624997 T>C did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:153958589 G>A maps to NM_002870.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr1:153958589 G>A maps to NM_002870.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr9:123953010 T>G did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr10:27793339 C>T maps to NM_021252.3 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr11:66039642 G>T maps to NM_030981.2 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr12:72163583 C>G maps to NM_014999.2 S55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr20:56918776 A>T maps to NM_020673.2 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:156035795 G>A maps to NM_020387.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:156038130 G>T maps to NM_020387.2 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr16:2203391 G>A maps to NM_014353.4 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr15:55527102 G>A maps to NM_183235.1 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr18:52556529 C>T maps to NM_004163.3 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr8:61504456 G>T maps to NM_002865.1 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr14:21945010 G>A maps to NM_032846.3 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr6:146875731 G>A maps to NM_006834.3 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr6:146865207 C>G maps to NM_006834.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr23:129318669 G>T did not map to a codon.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr23:129306269 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:129318669 G>C did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr4:140375393 C>T maps to NM_031296.1 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:140375561 A>T maps to NM_031296.1 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr4:140394009 T>C maps to NM_031296.1 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:140375450 C>T maps to NM_031296.1 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr17:27042681 G>C maps to NM_001144943.1 S176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr17:27042242 G>C maps to NM_001144943.1 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr17:27043999 C>A maps to NM_001144943.1 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr22:23503123 G>A maps to NM_004914.2 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr17:72738391 G>T did not map to a codon.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr17:72740490 G>T maps to NM_001006638.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr11:87847302 A>G maps to NM_022337.2 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr11:107832731 T>A maps to NM_017516.1 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr23:154490248 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr23:154493368 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr23:154493422 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr19:18311165 G>A maps to NM_002866.4 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr19:18308280 C>T maps to NM_002866.4 *221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr19:18311165 G>A maps to NM_002866.4 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:52442690 A>C maps to NM_002867.3 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr5:58021939 C>T maps to NM_138453.2 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr19:11447922 G>A maps to NM_004283.3 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:135922245 C>T maps to NM_001172435.1 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:135878475 C>T maps to NM_001172435.1 Q246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr2:135888196 C>G maps to NM_001172435.1 S381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr2:135890466 C>T maps to NM_001172435.1 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:220364530 G>A maps to ENST00000358951 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr1:220325066 G>A maps to ENST00000358951 Q1303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr1:220363788 G>A maps to ENST00000358951 Q521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:61672246 G>A maps to NM_013401.2 C255C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:61666828 G>A maps to NM_013401.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr12:70206616 C>G maps to NM_175623.2 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr23:102754906 A>G did not map to a codon.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr23:102192351 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr23:102192681 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:102192695 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:80616442 G>A maps to NM_006822.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:676020 C>T maps to NM_021168.4 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:677450 C>T maps to NM_021168.4 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:28920609 C>A maps to NM_001193532.1 S213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr1:28920463 C>T maps to NM_001193532.1 C164C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr3:128810172 G>A maps to NM_198490.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:41292603 C>T maps to ENST00000419646 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr19:41289873 C>T maps to ENST00000419646 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr12:56384494 G>T maps to NM_002868.2 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr17:40278827 G>A maps to NM_201434.1 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:73390758 G>A maps to NM_198896.1 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr3:133557042 C>T maps to NM_016577.3 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr3:133583442 G>A maps to NM_016577.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:130738131 G>A maps to NM_032144.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr3:128525357 C>T maps to NM_004637.5 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr15:63554898 T>C maps to NM_016530.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr23:13727080 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:13726929 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:103080329 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr23:103080408 C>T did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:103080335 C>T did not map to a codon.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr17:5257703 A>G maps to NM_004703.4 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr16:28919982 G>A maps to NM_024816.2 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr16:28925597 G>A maps to NM_024816.2 Q285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr16:28935727 C>T maps to NM_024816.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr9:125748548 C>T maps to NM_012197.3 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr1:174188318 G>A maps to NM_014857.3 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:174188321 G>A maps to NM_014857.3 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr7:66270178 C>T maps to ENST00000451741 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr7:66240336 G>A maps to ENST00000451741 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr7:66264315 G>A maps to ENST00000451741 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr14:24740141 C>T maps to NM_182836.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr14:24737147 G>A maps to NM_182836.1 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr14:24738748 G>A maps to NM_182836.1 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr14:24738892 G>A maps to NM_182836.1 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr1:76259860 C>T maps to NM_004582.2 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:76257180 C>T maps to NM_004582.2 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr2:114399704 G>A maps to ENST00000409875 *239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr22:51207204 C>G maps to NM_001130923.1 *239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:120424962 T>C did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:120461333 C>T maps to NM_173825.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr3:120461310 G>C maps to NM_173825.3 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr22:37627331 C>T maps to NM_002872.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr12:50390834 G>C maps to NM_013277.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr12:50384501 C>T maps to NM_013277.3 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr5:68684859 G>A did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr8:117864826 C>A maps to NM_006265.2 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:117875444 G>T maps to NM_006265.2 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:117875449 G>A maps to NM_006265.2 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr8:117878902 A>G maps to NM_006265.2 H22H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr8:117878848 G>A maps to NM_006265.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr8:117869587 C>G maps to NM_006265.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr8:117862988 C>T maps to NM_006265.2 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr19:13059905 G>A maps to NM_005053.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr19:13056770 C>T maps to NM_005053.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr19:13058998 C>A maps to NM_005053.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:13060210 C>T maps to NM_005053.2 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr9:110086240 T>C maps to NM_002874.3 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr9:110081036 G>T maps to NM_002874.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:131973863 G>A maps to NM_005732.3 L1189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr5:131931308 C>T maps to NM_005732.3 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr5:131925438 G>A maps to NM_005732.3 Q454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr5:131925447 G>A maps to NM_005732.3 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr2:17697672 G>A maps to NM_001099218.2 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr2:17697543 A>G maps to NM_001099218.2 C713C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr2:17699361 G>C maps to NM_001099218.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr17:56774140 T>C maps to NM_058216.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:56780671 C>T maps to NM_058216.1 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr17:33446593 G>C maps to NM_002878.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr17:33430493 G>A maps to NM_002878.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr8:95412468 A>G maps to NM_012415.2 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr8:95392432 G>T maps to NM_012415.2 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr8:95392460 G>C maps to NM_012415.2 S720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr8:95403935 G>A maps to NM_012415.2 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr8:95384565 T>A maps to NM_012415.2 P855P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr1:46725663 G>C maps to NM_003579.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:46725690 C>G maps to NM_003579.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr3:51673631 C>T maps to NM_015106.2 G686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr3:51667673 C>T maps to NM_015106.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:51664904 C>G maps to NM_015106.2 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:51697087 C>T maps to NM_015106.2 P1352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr3:51667732 C>T maps to NM_015106.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:51679709 G>A maps to NM_015106.2 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:67161231 G>A maps to NM_004584.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:110969421 C>T maps to NM_152442.3 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr7:4841584 C>T maps to NM_018059.4 P847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr7:4856875 G>A maps to NM_018059.4 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr7:4917470 G>T maps to NM_018059.4 Y100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:4917719 C>T maps to NM_018059.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr7:4876159 C>T maps to NM_018059.4 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr7:4876216 C>A maps to NM_018059.4 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr7:4839011 G>C maps to NM_018059.4 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr7:4845212 G>C maps to NM_018059.4 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:4856950 C>T maps to NM_018059.4 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:150210658 G>C maps to NM_139165.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr6:150209696 G>A maps to NM_139165.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr6:150210553 G>C maps to NM_139165.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:150211198 C>T maps to NM_139165.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:150342221 G>C maps to NM_130900.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:12633229 G>A maps to ENST00000415519 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr3:12626635 G>A maps to ENST00000415519 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:12641740 C>G maps to ENST00000415519 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:12650383 G>A maps to ENST00000415519 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr11:36595000 G>A maps to NM_000448.2 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr11:36594952 C>T maps to NM_000448.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr11:36595983 C>G maps to NM_000448.2 S377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:155109405 T>C maps to NM_018845.3 Y87Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:155110755 G>C maps to NM_018845.3 *222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr11:36614269 C>T maps to NM_000536.3 E483E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr11:36614206 G>T maps to NM_000536.3 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr11:36614599 C>T maps to NM_000536.3 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr14:102749864 C>G maps to NM_014226.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr14:102718330 C>G maps to NM_014226.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr17:17699028 G>T maps to ENST00000395776 E923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr17:17697754 C>G maps to ENST00000395776 S498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:17699981 C>G maps to ENST00000395776 V1240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:17700284 C>G maps to ENST00000395776 L1341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:17701367 C>T maps to ENST00000395776 L1702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:17700428 G>A maps to ENST00000395776 Q1389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr17:17697754 C>G maps to ENST00000395776 S498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr17:17700284 C>G maps to ENST00000395776 L1341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr17:17697727 C>G maps to ENST00000395776 S489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr5:34823481 C>G maps to NM_001145521.1 S512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr23:17819600 G>A did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:17819187 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:17819643 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr2:121043652 A>G maps to NM_002881.2 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr18:9516933 C>T maps to NM_006788.3 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr18:9522254 G>A maps to NM_006788.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr18:9522191 C>G maps to NM_006788.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr18:9525818 C>T maps to NM_006788.3 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr14:36230212 C>A did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr14:36219783 G>A maps to NM_194301.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr14:36277975 C>T maps to NM_194301.2 K22K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:20621417 G>A maps to NM_020343.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:20563780 C>A maps to NM_020343.3 E874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr20:20582437 G>A maps to NM_020343.3 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr20:20475835 G>C maps to NM_020343.3 A1764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr20:20484036 G>A maps to NM_020343.3 S1722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr20:20656891 G>T maps to NM_020343.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr20:37182715 G>A maps to NM_020336.2 L1123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:37128102 G>A maps to NM_020336.2 E189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr20:37177330 G>A did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr20:37126020 C>T maps to NM_020336.2 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr20:37117125 C>T maps to NM_020336.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr20:37153560 C>A maps to NM_020336.2 S587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr20:37154109 C>T maps to NM_020336.2 I617I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr20:37203507 G>A maps to NM_020336.2 Q1461Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr20:37202941 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr20:37174948 G>A maps to NM_020336.2 V926V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr9:135985047 G>A maps to NM_006266.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr9:135983458 T>A maps to NM_006266.2 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr9:135973979 G>A maps to NM_006266.2 I913I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:129815196 C>T maps to NM_014636.2 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr20:32664891 C>T maps to NM_016732.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:85441684 A>G maps to NM_001100391.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:238785965 C>T maps to NM_005855.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr17:40913917 G>A did not map to a codon.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr12:131359241 G>A maps to ENST00000392369 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr22:20106565 G>T maps to NM_002882.2 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr16:67763851 G>C maps to NM_020850.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:67768936 G>C maps to NM_020850.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr16:67761245 G>C maps to NM_020850.1 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:170351477 C>T maps to NM_022897.3 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr5:170669744 T>C maps to NM_022897.3 H899H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr5:170341201 C>T maps to NM_022897.3 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr5:170319553 C>G maps to NM_022897.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr5:170610194 G>A maps to NM_022897.3 V630V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr5:170343485 T>C maps to NM_022897.3 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr5:170380671 G>T maps to NM_022897.3 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr5:170722895 C>T maps to NM_022897.3 F1016F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr5:170722904 G>A maps to NM_022897.3 L1019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:109398639 A>G maps to NM_006267.4 K2939K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:109383782 C>G maps to NM_006267.4 S2263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr2:109381657 C>T maps to NM_006267.4 R1555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:109383108 G>A maps to NM_006267.4 Q2038Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:109388218 C>T maps to NM_006267.4 L2638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr2:109379690 A>G did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:109392267 T>C maps to NM_006267.4 C2791C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr2:109336128 C>T maps to NM_006267.4 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:5941639 G>C maps to NM_007322.2 S133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr19:5923855 C>A maps to NM_007322.2 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:36255643 C>A maps to NM_001161429.1 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:36265594 G>C maps to NM_001161429.1 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr5:36257639 G>A maps to NM_001161429.1 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr5:36251540 G>A maps to NM_001161429.1 Q435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr9:6013639 C>A maps to NM_012416.2 V656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:6014800 C>T maps to NM_012416.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr9:6012362 A>T maps to NM_012416.2 L1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr6:13625941 G>A maps to NM_005493.2 Q668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr22:41657563 G>A maps to NM_002883.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr22:41645813 C>T maps to NM_002883.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr22:41650328 G>A maps to NM_002883.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:21937962 C>T maps to NM_001145658.1 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr1:21929364 C>T maps to NM_001145658.1 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:21940119 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:21938309 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr17:2867250 G>T maps to NM_015085.4 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr17:2868928 C>T maps to NM_015085.4 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr17:2867286 C>T maps to NM_015085.4 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr4:99325709 G>A maps to NM_001100426.1 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr4:99325665 G>T maps to NM_001100426.1 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:98086807 C>T maps to NM_021033.6 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr13:98086978 C>T maps to NM_021033.6 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:152880937 G>A maps to NM_002886.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:152880886 T>C maps to NM_002886.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:152880589 C>T maps to NM_002886.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr23:131348328 C>A did not map to a codon.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:131351025 G>A did not map to a codon.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:131351112 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr23:131351281 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr9:134497233 G>T maps to NM_198679.1 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:134454940 C>G maps to NM_198679.1 L1077L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr9:134501393 G>C maps to NM_198679.1 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr9:134501606 A>G maps to NM_198679.1 D469D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr4:160260432 G>T maps to NM_014247.2 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr4:160253616 C>T maps to NM_014247.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr4:160264206 C>T maps to NM_014247.2 Q838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:160262845 C>T maps to NM_014247.2 R728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:48132487 G>A maps to NM_001098531.2 I837I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:48134147 G>A maps to NM_001098531.2 F754F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FH-01A-11D-A38G-08 chr12:48134126 G>A maps to NM_001098531.2 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr12:48131868 G>A maps to NM_001098531.2 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr2:173881123 C>G maps to NM_007023.3 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47W-01A-11D-A23U-08 chr2:173881075 G>T did not map to a codon.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr2:173782570 T>C maps to NM_007023.3 Y162Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr2:173883402 C>A maps to NM_007023.3 C676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr2:173901377 G>A maps to NM_007023.3 G937G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr7:22165246 C>G maps to ENST00000344041 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr7:22176589 C>T maps to ENST00000344041 G612G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:22259537 C>A maps to ENST00000344041 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr7:22233636 C>G maps to ENST00000344041 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr5:130846087 G>A maps to ENST00000514667 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:130825319 C>A maps to ENST00000514667 E637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:130764700 G>A maps to ENST00000514667 L1608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:130846054 G>A maps to ENST00000514667 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr5:130808289 G>C maps to ENST00000514667 S793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr17:38347662 C>T maps to ENST00000456989 H476H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr17:38346911 C>T maps to ENST00000456989 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:38349979 C>T maps to ENST00000456989 V642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:204354804 C>T maps to ENST00000374493 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:204360076 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr3:25637930 T>C maps to NM_000965.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:53607343 G>A maps to NM_000966.4 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:53609124 G>A maps to NM_000966.4 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:53607027 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:53608273 G>A maps to NM_000966.4 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:53607866 G>C maps to NM_000966.4 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr12:53621230 G>A maps to NM_000966.4 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr12:53609098 G>A maps to NM_000966.4 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:53607385 G>A maps to NM_000966.4 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:53607343 G>A maps to NM_000966.4 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:53607866 G>A maps to NM_000966.4 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:53605597 A>G maps to NM_000966.4 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr3:158431618 G>A maps to NM_206963.1 H102H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr7:150037206 G>A maps to NM_002889.3 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:63312135 G>A maps to NM_004585.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr5:167919788 G>A maps to NM_002887.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr6:88258312 G>A maps to NM_020320.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr5:86679589 C>T maps to NM_002890.1 I917I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:141272698 C>T maps to ENST00000452898 H176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:141328357 G>A maps to ENST00000452898 K775K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:141259400 G>C maps to ENST00000452898 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr3:141248609 C>A maps to ENST00000452898 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr3:141272767 A>C maps to ENST00000452898 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr13:114776712 C>T maps to ENST00000389544 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BS-01A-21D-A26M-08 chr13:114782769 G>A maps to ENST00000389544 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr13:114762071 C>A maps to ENST00000389544 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr13:114751216 C>T maps to ENST00000389544 S773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr13:114789774 G>A maps to ENST00000389544 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr12:113554885 C>T maps to NM_001193520.1 E241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:178433411 G>A did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:178269182 G>A maps to ENST00000263528 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:178420826 C>T maps to ENST00000263528 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:15567439 C>T maps to NM_022904.1 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:15562864 C>T maps to NM_022904.1 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr22:35947614 C>T maps to NM_014310.3 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:35947784 C>T maps to NM_014310.3 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr9:85677429 G>T maps to NM_152573.2 S118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr10:43696156 G>A maps to ENST00000374459 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr4:82368723 G>A maps to NM_152545.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr4:82378748 G>A maps to NM_152545.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr4:82355882 C>T maps to NM_152545.1 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr5:179564992 G>T maps to NM_175062.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr5:179555573 G>A maps to NM_175062.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr5:179546349 G>T maps to NM_175062.3 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr15:79284124 C>T maps to NM_002891.4 V1029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr15:79272966 C>T maps to NM_002891.4 L1179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr15:79356817 C>T maps to NM_002891.4 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr15:79296351 G>A maps to NM_002891.4 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr15:79264242 G>A maps to NM_002891.4 Q1232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr15:79310117 G>A maps to NM_002891.4 I579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:79327529 G>A maps to NM_002891.4 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr15:79339116 G>A maps to NM_002891.4 H283H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr5:80390804 C>A maps to NM_006909.1 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr5:80369169 C>T maps to NM_006909.1 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr5:80422971 G>C maps to NM_006909.1 G892G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr5:80409488 G>C maps to NM_006909.1 V740V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr5:80256709 C>G maps to NM_006909.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr5:80419515 G>A maps to NM_006909.1 A842A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr15:38852030 G>A maps to NM_005739.3 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr15:38793448 G>A maps to NM_005739.3 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr11:64502636 G>A maps to ENST00000320253 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr11:64494817 C>A maps to ENST00000320253 E657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:64507206 G>A maps to ENST00000320253 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr11:64507277 G>A maps to ENST00000320253 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr2:33741657 G>A maps to NM_170672.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:38901618 G>T maps to ENST00000405332 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:38900724 C>T maps to ENST00000405332 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr19:38901776 T>A maps to ENST00000405332 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:49238512 G>A maps to NM_017805.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:49238542 G>A maps to NM_017805.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr19:49225141 A>G maps to NM_017805.2 P887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr19:49224144 G>A maps to NM_017805.2 L934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr22:29709883 C>G maps to NM_006477.3 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr17:34068248 C>A maps to NM_033315.3 C179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr4:53730718 C>T maps to NM_023940.2 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr15:65360143 C>G maps to NM_016563.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr15:65347257 C>T maps to NM_016563.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr3:50368086 G>T maps to NM_170714.1 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr3:50368146 G>A maps to NM_170714.1 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr20:4768392 C>T maps to NM_014737.2 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr20:4776582 G>C maps to NM_014737.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:74453626 G>A maps to NM_201431.1 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr4:74442169 A>G maps to NM_201431.1 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr11:561797 G>T maps to NM_003475.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr12:86199358 G>A maps to NM_005447.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:86198925 C>A maps to NM_005447.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:10431552 G>C maps to NM_133452.2 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr19:10432222 G>A maps to NM_133452.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr19:10431735 C>T maps to NM_133452.2 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:65243753 C>T maps to ENST00000294428 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr13:49050905 G>T maps to NM_000321.2 E864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr13:49039500 C>G maps to NM_000321.2 S829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr13:49047506 C>A maps to NM_000321.2 S834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr13:48955393 C>T maps to NM_000321.2 Q504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr13:48881461 C>T maps to NM_000321.2 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr13:49050863 C>T maps to NM_000321.2 Q850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr13:48947628 G>T did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr13:48947628 G>C did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr13:49027247 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr13:48955537 C>T maps to NM_000321.2 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr13:49039353 C>A maps to NM_000321.2 S780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr13:48947628 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr13:48947602 C>G maps to NM_000321.2 S397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr13:48936994 C>T maps to NM_000321.2 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr13:48951052 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr13:49039214 A>T maps to NM_000321.2 K765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr13:49050845 A>T maps to NM_000321.2 K844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr13:48936982 C>T maps to NM_000321.2 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr13:49047506 C>G maps to NM_000321.2 S834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr13:48941647 C>T maps to NM_000321.2 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr13:48953768 G>T maps to NM_000321.2 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr13:49027247 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr13:48941632 G>T maps to NM_000321.2 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr13:48953759 C>T maps to NM_000321.2 R455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr13:48947539 G>C did not map to a codon.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr13:49037931 T>A maps to NM_000321.2 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr13:49050863 C>T maps to NM_000321.2 Q850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr13:48947584 C>G maps to NM_000321.2 S391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr13:48934193 C>T maps to NM_000321.2 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr13:49050980 T>C did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr13:49037965 C>T maps to NM_000321.2 Q736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr13:49033933 G>T maps to NM_000321.2 E691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr13:48947538 A>G did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr13:49033861 G>T maps to NM_000321.2 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr13:48934193 C>T maps to NM_000321.2 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr13:49050980 T>G did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr13:49037865 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr13:49039157 G>T maps to NM_000321.2 E746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr13:48919280 C>G maps to NM_000321.2 S149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr13:49030425 C>A maps to NM_000321.2 S634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr13:48953729 C>T maps to NM_000321.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr13:49050874 T>A maps to NM_000321.2 C853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr13:48953728 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr13:48955558 G>T maps to NM_000321.2 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr13:48939095 G>T maps to NM_000321.2 G310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr13:48881434 G>T maps to NM_000321.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr13:48954209 C>T maps to NM_000321.2 Q471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr13:49047506 C>A maps to NM_000321.2 S834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr13:48947628 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr13:49039461 C>G maps to NM_000321.2 S816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr13:49039229 C>T maps to NM_000321.2 Q770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr13:49039247 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:53568832 C>A maps to NM_014781.4 E1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr8:53573711 G>A maps to NM_014781.4 Y496Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr8:53569250 T>C maps to NM_014781.4 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr8:53568650 T>C maps to NM_014781.4 L1246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr8:53569703 C>T maps to NM_014781.4 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr8:53570252 C>T maps to NM_014781.4 Q712Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr8:53555080 G>A maps to NM_014781.4 V1389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:33138429 C>T maps to NM_005610.2 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr1:33145305 G>C maps to NM_005610.2 *426Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:33134688 T>C maps to NM_005610.2 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:33135115 G>A maps to NM_005610.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr1:33134445 A>C maps to NM_005610.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:24567225 C>T maps to NM_006910.4 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr16:24582656 C>T maps to NM_006910.4 Q1424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:24564832 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:24583381 G>C maps to NM_006910.4 L1665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:24583381 G>C maps to NM_006910.4 L1665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr16:24582457 A>C maps to NM_006910.4 S1357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr16:24567012 C>G maps to NM_006910.4 Y142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:16864053 T>A did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr23:16887337 C>G did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:16864006 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:16876950 A>G did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:16881164 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr23:16887314 G>C did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:16876879 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr18:20606178 A>C maps to ENST00000360790 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr18:20581687 A>G maps to ENST00000360790 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr18:20573152 G>T maps to ENST00000360790 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr18:20586356 G>A maps to ENST00000360790 Q778Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr20:408111 C>T maps to NM_031229.2 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr20:390663 C>T maps to NM_031229.2 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:28113130 G>A maps to NM_022128.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr2:28065997 G>T maps to NM_022128.1 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr20:35627251 T>A maps to NM_002895.2 A1039A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:35627226 G>A maps to NM_002895.2 Q1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr20:35724277 C>A maps to NM_002895.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr20:35717440 C>A maps to NM_002895.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr20:35690594 G>A maps to NM_002895.2 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr16:53495736 C>T maps to NM_005611.3 D477D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr16:53524210 G>A maps to NM_005611.3 *1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:53495719 C>T maps to NM_005611.3 Q472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:53498193 C>G maps to NM_005611.3 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr16:53495762 G>A did not map to a codon.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr23:47039403 C>T did not map to a codon.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr23:47044969 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr23:47041569 A>C did not map to a codon.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr23:47041368 C>G did not map to a codon.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr23:47045532 A>T did not map to a codon.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr23:47038855 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr23:47030581 G>T did not map to a codon.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr23:47045023 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:47044501 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr23:47045005 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr23:47045490 G>A did not map to a codon.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr23:47044999 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr23:47041575 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:47045540 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr23:47038525 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr23:47044530 C>A did not map to a codon.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr23:47028823 C>A did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr23:47045015 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:47038821 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr23:47040800 G>T did not map to a codon.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr23:47030648 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr23:47030516 C>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr21:15599289 G>A maps to NM_144770.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr21:15599415 G>A maps to NM_144770.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr20:34242689 G>T maps to NM_001198838.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr8:94748074 A>G maps to NM_203390.2 H188H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr8:94747018 G>A maps to NM_203390.2 F540F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr8:94747018 G>A maps to NM_203390.2 F540F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr8:94747050 G>A maps to NM_203390.2 Q530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr8:94747100 G>C maps to NM_203390.2 S513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr11:66384202 C>T maps to NM_001198845.1 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr1:110882413 G>A maps to NM_022768.4 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:110882503 A>G maps to NM_022768.4 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:110882502 C>G maps to NM_022768.4 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:110882101 G>C maps to NM_022768.4 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr1:110882242 G>A maps to NM_022768.4 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:110882178 C>A maps to NM_022768.4 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr3:51430788 C>T maps to NM_013286.4 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr3:51429186 G>T maps to NM_013286.4 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47W-01A-11D-A23U-08 chr6:155123134 C>T maps to NM_014892.3 Q213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:155143462 C>T maps to NM_014892.3 Q616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr6:155145432 G>A maps to NM_014892.3 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:6143280 G>A maps to NM_001145547.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr10:6151978 C>G maps to NM_001145547.1 S198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:6154211 C>T maps to NM_001145547.1 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr10:6155491 C>G maps to NM_001145547.1 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr9:125009804 G>A maps to NM_033117.3 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:114392941 G>A maps to NM_016196.3 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:114358487 G>C maps to NM_016196.3 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr12:114400180 G>A maps to NM_016196.3 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr12:114261118 C>T maps to NM_016196.3 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr14:23371024 G>A maps to NM_001077351.1 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr6:17292230 C>T maps to NM_001143942.1 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr14:73576062 C>T maps to NM_021239.2 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr13:79916955 G>C maps to ENST00000438737 S758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:79951554 C>A maps to ENST00000438737 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr5:145651075 C>T maps to NM_018989.1 R943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:145598617 G>T maps to NM_018989.1 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:145665547 C>T maps to NM_018989.1 D1046D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr5:145649131 G>A maps to NM_018989.1 V892V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr5:145616995 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:145608581 C>G maps to NM_018989.1 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:127978388 C>T maps to NM_018077.2 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:127953305 C>G maps to NM_018077.2 V689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr7:127965870 C>T maps to NM_018077.2 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr7:155534733 G>A maps to NM_053043.2 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr1:235299017 C>T maps to NM_015014.2 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:235298996 G>A maps to NM_015014.2 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:235318294 G>A maps to NM_015014.2 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr20:55982649 G>A maps to NM_017495.4 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr20:55982880 G>A maps to NM_017495.4 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr20:34312509 G>A maps to NM_184234.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr20:34292503 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr20:34302203 C>G maps to NM_184234.1 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:66410997 C>A maps to NM_001198845.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr11:66407490 G>A maps to NM_002896.3 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr23:106359926 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr19:36120514 G>C maps to NM_024321.3 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:36128213 G>A maps to NM_024321.3 K430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:36124153 G>T maps to NM_024321.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:152109295 A>G maps to NM_198557.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:238726128 C>T maps to NM_001080504.2 H190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr2:238726012 C>T maps to NM_001080504.2 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr2:178981041 A>G maps to ENST00000456670 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr2:178990896 T>G maps to ENST00000456670 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr4:40440103 G>A maps to NM_001098634.1 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr4:40440405 C>A maps to NM_001098634.1 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr4:40440304 C>T maps to NM_001098634.1 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr4:40439967 G>A maps to NM_001098634.1 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr4:40440384 C>A maps to NM_001098634.1 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:66444532 G>A maps to NM_031492.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr3:50151424 C>T maps to NM_005778.2 Q554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr3:50150943 G>A maps to NM_005778.2 K528K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr3:50144984 C>T maps to NM_005778.2 Q342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr3:50145734 C>G maps to NM_005778.2 S397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr3:50103757 G>A maps to NM_005777.2 Q922Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:50005787 G>A maps to NM_005777.2 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr3:50095161 G>A maps to NM_005777.2 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr3:50095428 G>A maps to NM_005777.2 E654E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr1:145508607 G>A maps to NM_005105.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr1:145508205 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:36164306 G>A maps to NM_001082578.1 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr22:36141975 G>A maps to NM_001082578.1 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:56982079 T>C maps to NM_002898.3 Y355Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr3:29476271 C>A maps to NM_001003793.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr3:29781208 A>T did not map to a codon.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr23:135957455 T>C did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:135956334 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr23:135957438 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr23:129545340 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr23:129537823 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr23:129546578 G>T did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:89449392 C>T maps to NM_019610.5 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr11:7110383 C>T maps to NM_014469.4 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:139258347 C>T maps to NM_002899.3 W71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr3:139195265 C>T maps to NM_004164.2 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr10:48387931 G>A maps to NM_002900.2 A982A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr10:48390280 G>T maps to NM_002900.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr10:48390772 G>A maps to NM_002900.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr10:48388816 T>A maps to NM_002900.2 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr10:48388318 C>T maps to NM_002900.2 E853E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr10:48390166 G>A maps to NM_002900.2 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr10:95360686 G>A maps to NM_006744.3 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr10:95353760 G>A maps to NM_006744.3 Y129Y. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-ZF-A9RC-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:95360731 C>T maps to ENST00000371463 T16T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-ZF-AA4V-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr10:95360731 C>T maps to ENST00000371463 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:10067688 G>A maps to ENST00000377192 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr1:10068238 T>C maps to ENST00000377192 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr20:43940279 G>A maps to NM_014276.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr20:43941003 G>T maps to NM_014276.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr20:43945385 C>G maps to NM_014276.2 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr20:43936861 C>T maps to NM_014276.2 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr22:41347431 G>C maps to NM_014248.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:173916677 G>A maps to NM_172071.2 Q856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr1:173916584 T>A maps to NM_172071.2 K887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:173953688 C>T maps to NM_172071.2 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr1:173910449 T>C maps to NM_172071.2 P1068P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr1:173952640 G>A maps to NM_172071.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr1:173934023 T>C maps to NM_172071.2 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:125621300 C>A maps to NM_001100588.1 E644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:125643057 C>A maps to NM_001100588.1 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr9:125617569 G>C maps to NM_001100588.1 S903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr21:35895990 G>C maps to NM_004414.5 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr6:46214587 G>C maps to ENST00000405162 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr6:46216492 G>A maps to ENST00000405162 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:24857724 C>G maps to NM_013441.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr13:50125589 G>A maps to NM_018191.3 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:49085971 G>A maps to NM_001268.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr13:49076926 G>A maps to NM_001268.2 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr13:49075960 T>C maps to NM_001268.2 E387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:28863400 G>A maps to NM_001048194.2 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr15:91500712 G>A maps to NM_033544.2 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:66612481 C>T maps to NM_005133.2 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:76434445 G>A maps to NM_015436.2 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr4:76439459 G>A maps to NM_015436.2 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:50046468 G>A maps to NM_020650.2 *329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr14:103187658 C>T maps to NM_015156.2 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr11:63682202 C>T maps to NM_173587.3 W135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr1:211433477 C>A maps to NM_001136223.1 Y65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:211486788 G>A maps to NM_001136223.1 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:167653185 C>A maps to NM_052862.3 S19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:167654656 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr1:167666544 G>A maps to NM_052862.3 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr17:9808389 C>A maps to NM_002903.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr1:211652650 C>T maps to NM_183059.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr8:74231401 G>A maps to NM_172037.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr14:68159212 C>G maps to NM_016026.3 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:68159245 C>T maps to NM_016026.3 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr14:68157130 G>A maps to NM_016026.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr14:68157902 C>T maps to NM_016026.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:68196079 G>C maps to NM_152443.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:55570558 G>A maps to NM_001145971.1 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr12:57348752 G>T maps to NM_003708.3 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:57345866 G>A maps to NM_003708.3 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr12:56115488 G>A maps to NM_002905.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:34251716 C>T maps to NM_145654.3 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr17:34251641 G>A maps to NM_145654.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:110128892 T>G maps to ENST00000405097 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr14:24648091 G>A maps to NM_005132.2 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr14:24647295 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:24641957 C>T maps to NM_005132.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:24648857 C>T maps to NM_005132.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr14:24648049 C>G maps to NM_005132.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr14:24642119 C>G maps to NM_005132.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr14:24642245 C>G maps to NM_005132.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr9:36118869 C>T maps to NM_021111.2 V790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:36109987 C>A maps to NM_021111.2 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:21624537 G>A maps to NM_032941.2 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr8:145737808 G>C maps to ENST00000428558 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr8:145741410 C>T maps to ENST00000428558 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr8:145737118 C>T maps to ENST00000428558 L1149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr8:145738371 C>T maps to ENST00000428558 E871E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr8:145739713 C>T maps to ENST00000428558 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr8:145737859 G>C maps to ENST00000428558 V990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr8:145737106 C>T maps to ENST00000428558 E1153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr8:145737615 G>A maps to ENST00000428558 D1049D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:73623519 C>T maps to NM_004259.5 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr17:73647279 G>A maps to NM_004259.5 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr17:73658558 C>A maps to NM_004259.5 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:86459889 G>A maps to NM_022912.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr10:65369971 T>G maps to NM_001001330.2 L148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:65354540 C>T maps to NM_001001330.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:21997684 C>T maps to NM_025232.2 W61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr8:21996544 C>T maps to NM_025232.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr5:112257851 G>A maps to NM_005669.4 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr5:112238166 C>G maps to NM_005669.4 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr5:112214530 C>T maps to NM_005669.4 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr2:79348724 C>T maps to NM_002909.4 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr2:79348028 G>C maps to NM_002909.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr2:79348719 C>A maps to NM_002909.4 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:79312627 A>C maps to NM_006507.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr2:79314042 C>T maps to NM_006507.3 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr2:79313603 G>T maps to NM_006507.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:79385577 C>T maps to NM_138937.2 Q69Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr2:79385895 C>T did not map to a codon.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr2:79386454 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr2:79384716 C>T maps to NM_138937.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:79253869 A>T maps to NM_001008387.1 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr2:61118920 G>A maps to NM_002908.2 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:65422346 G>A maps to NM_021975.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:65422352 G>A maps to NM_021975.3 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:65427189 G>C maps to NM_021975.3 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr19:45535843 C>T maps to ENST00000221452 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr19:45535936 C>T maps to ENST00000221452 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:45535909 G>A maps to ENST00000221452 E370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr19:45540669 C>T maps to ENST00000221452 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr19:45540801 C>G maps to ENST00000221452 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr4:37687843 C>T maps to NM_001085399.1 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr5:141017938 G>A maps to NM_173828.4 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr7:103197508 C>T maps to ENST00000428762 T1904T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr7:103301856 G>A maps to ENST00000428762 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr7:103198484 C>T maps to ENST00000428762 R1847R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr7:103202300 C>T maps to ENST00000428762 W1770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr7:103281033 G>C maps to ENST00000428762 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr7:103126789 G>C maps to ENST00000428762 T3279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr7:103191698 C>G maps to ENST00000428762 V2039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr7:103113312 A>G maps to ENST00000428762 H3443H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr7:103131251 C>T maps to ENST00000428762 Q3156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:73102215 C>T maps to NM_152222.1 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr11:73102206 G>A maps to NM_152222.1 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr20:30065712 G>A maps to NM_014012.4 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:204129687 G>C maps to NM_000537.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:204125004 G>A maps to NM_000537.3 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr1:204125341 G>A maps to NM_000537.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr23:153205629 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr23:153206996 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:153205671 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:153207432 G>T did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr23:153209863 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr12:27849659 G>C maps to NM_001029874.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:150068791 C>T maps to NM_001099695.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:150068726 C>T maps to NM_001099695.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:17080620 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr23:17040286 G>A did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:17088066 G>C did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:17088106 G>C did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:17095460 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr23:17047693 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr23:17024394 T>C did not map to a codon.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr1:2327261 C>T maps to NM_007033.4 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr1:2328586 C>T maps to NM_007033.4 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr1:8601298 G>A maps to NM_012102.3 Y268Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:8415170 C>T maps to NM_012102.3 K1559K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr12:15262115 C>T maps to NM_032918.2 K176K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:18241851 C>A maps to NM_024730.2 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr4:57797924 A>G maps to NM_005612.4 E967E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr4:57798294 G>T maps to NM_005612.4 E1091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr4:57797246 G>A maps to NM_005612.4 Q741Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:43612093 C>T maps to NM_020975.4 G733G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:7734743 G>A maps to NM_020415.3 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr19:7734265 C>T maps to NM_020415.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr2:85571796 G>T maps to NM_017750.3 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr2:100040680 G>A maps to NM_016316.2 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr2:100020191 C>T maps to NM_016316.2 E1044E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:100019386 G>A maps to NM_016316.2 L1117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:100020218 C>T maps to NM_016316.2 A1035A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr6:111650797 C>A maps to NM_002912.3 L2726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr6:111688579 T>C maps to NM_002912.3 K2137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:111702566 G>A maps to NM_002912.3 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr6:111694064 G>A maps to NM_002912.3 D1831D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr6:111699000 G>A maps to NM_002912.3 D500D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr6:111628631 G>A maps to NM_002912.3 Q3062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr6:111697610 G>A maps to NM_002912.3 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:111631229 C>T maps to NM_002912.3 G2956G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr6:111694546 G>A maps to NM_002912.3 Q1671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr6:111697647 G>C maps to NM_002912.3 S637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:1818819 G>A maps to NM_020695.3 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:1827791 G>A maps to NM_020695.3 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:1825876 C>T maps to NM_020695.3 Q659Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:1825897 C>G maps to NM_020695.3 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr19:1817223 G>A maps to NM_020695.3 C1065C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:1816245 G>C maps to NM_020695.3 L1185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr19:1818732 G>A maps to NM_020695.3 F958F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr11:114315273 C>G maps to NM_015523.3 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:114310357 G>A maps to NM_015523.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr9:136282823 C>T maps to NM_020385.2 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr9:136277902 G>A maps to NM_020385.2 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr7:73646461 T>A maps to NM_181471.1 K347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr13:34410250 C>A maps to NM_002915.3 S297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr3:186507802 G>A maps to NM_181573.2 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:118456875 G>C did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr9:79003560 G>A maps to ENST00000257452 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr22:29835055 C>T maps to NM_021026.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr22:29834845 C>T maps to NM_021026.2 C22C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr22:29834878 C>T maps to NM_021026.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr22:29837966 C>T maps to NM_021026.2 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr22:32587016 C>T maps to NM_001098527.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr22:32587286 G>A maps to NM_001098527.2 D203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr22:32756542 C>G maps to NM_001098535.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:53157762 C>T maps to NM_052859.3 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:53159983 G>A maps to NM_052859.3 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:53133473 G>C maps to NM_052859.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr3:53139696 G>A maps to NM_052859.3 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:53125963 G>A maps to NM_052859.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:53133431 G>A maps to NM_052859.3 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr3:53133452 G>A maps to NM_052859.3 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr3:16475482 G>A maps to NM_015150.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:16535314 G>C maps to NM_015150.1 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr3:16411601 G>A maps to NM_015150.1 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:198498568 C>T maps to NM_144629.2 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:198508943 C>A maps to NM_144629.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:198498721 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:198495895 G>T maps to NM_144629.2 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr1:175996747 G>A maps to NM_022457.5 F563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:176133010 A>G maps to NM_022457.5 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:175956093 C>T maps to NM_022457.5 R706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr16:74670450 G>A maps to NM_018124.3 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr16:74685991 G>A maps to NM_018124.3 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr16:74695238 G>A maps to NM_018124.3 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:74678297 C>T maps to NM_018124.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr16:74671789 G>A maps to NM_018124.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr19:14094345 C>T maps to NM_002918.4 Q127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr19:14076444 G>A maps to NM_002918.4 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:14079425 C>T maps to NM_002918.4 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr19:14076338 G>A maps to NM_002918.4 I711I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr19:5994917 G>A maps to NM_000635.3 D700D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:6007098 C>T maps to NM_000635.3 W442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:3257089 C>T maps to NM_134428.1 W572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:3248112 G>C maps to NM_134428.1 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr9:3288250 C>G did not map to a codon.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr12:107105269 C>G maps to ENST00000357881 S334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:106977136 C>A maps to NM_213594.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:151316208 G>A maps to NM_000449.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:117198479 G>A maps to NM_173560.3 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:117232128 C>G maps to NM_173560.3 S235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr6:117250118 C>T maps to NM_173560.3 R866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr15:56387672 T>G maps to NM_022841.5 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr15:56434994 C>A maps to NM_022841.5 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr15:56388200 T>A maps to NM_022841.5 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:19308933 C>T maps to NM_003721.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr13:37394042 G>A maps to NM_000538.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr13:37393935 G>T maps to NM_000538.3 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr4:100477341 C>T maps to NM_001134666.1 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:100479302 G>C maps to NM_001134666.1 S84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr4:100479210 A>G maps to NM_001134666.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr4:100474980 G>C maps to NM_001134666.1 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr9:37770007 C>G maps to NM_144964.2 S215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:37776349 C>T maps to NM_144964.2 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr9:37777700 A>G maps to NM_144964.2 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:109695176 C>G did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr23:109697167 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr23:109695850 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:109697882 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr23:109695910 C>G did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:109694610 T>C did not map to a codon.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr23:109697192 A>G did not map to a codon.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr23:109697828 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr23:109695649 C>A did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr23:71350505 G>T did not map to a codon.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr23:71351226 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:71350615 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:183853907 C>T maps to NM_015149.3 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:183885720 G>A maps to NM_015149.3 V665V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr1:183853948 C>T maps to NM_015149.3 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr1:183711300 G>A maps to NM_015149.3 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:183849900 G>T maps to NM_015149.3 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr6:33262909 G>T maps to NM_004761.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr19:11526624 G>A maps to NM_001161616.1 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr19:11510900 G>A maps to NM_001161616.1 I519I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr22:24038811 T>C maps to ENST00000382833 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr22:24040398 G>T maps to ENST00000382833 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr15:93588793 C>A maps to NM_020211.2 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr15:93595603 C>T maps to NM_020211.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:93595351 C>T maps to NM_020211.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr15:93588524 G>T maps to NM_020211.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr15:93588488 G>T maps to NM_020211.2 C364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr5:98115320 A>G maps to NM_001012761.2 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr23:46951123 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr5:73142263 T>C maps to NM_001080479.2 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr9:35752110 C>T maps to ENST00000456972 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr9:35752708 C>G maps to ENST00000456972 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:87141007 C>T maps to NM_001078170.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr2:107084738 A>G maps to ENST00000304514 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr2:107084703 G>T maps to ENST00000304514 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr2:108487486 T>A maps to NM_182588.2 G1009G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:113146030 T>C maps to NM_005054.2 E1497E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:86004863 C>T maps to ENST00000358110 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr16:321236 G>C maps to NM_183337.1 S276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr4:3318388 G>A maps to NM_198229.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr4:3318689 G>T maps to NM_198229.2 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr4:3318694 G>A maps to NM_198229.2 Q266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr4:3318745 G>C maps to NM_198229.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr4:3318787 G>A maps to NM_198229.2 E297E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr4:3318865 G>C maps to NM_198229.2 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr4:3416498 C>T maps to NM_198229.2 F737F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:3344755 C>T maps to NM_198229.2 I658I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:3319681 G>A maps to NM_198229.2 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr4:3319745 C>T maps to NM_198229.2 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr4:3424263 G>A maps to NM_198229.2 A1000A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr4:3424660 C>T maps to NM_198229.2 I1021I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr4:3344705 C>T maps to NM_198229.2 Q642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr4:3318781 G>T maps to NM_198229.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr1:192628535 T>C maps to NM_144766.2 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr1:192627376 C>T maps to NM_144766.2 D58D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr5:176794806 C>T maps to ENST00000398128 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:192150525 C>T maps to NM_130782.2 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr1:192153582 G>T maps to NM_130782.2 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr8:54866818 G>A maps to NM_170587.2 E309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:192321193 C>T maps to NM_001039152.3 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr8:101020779 G>A maps to NM_015668.3 Y728Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:101083754 A>G maps to NM_015668.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr8:101078405 G>T maps to NM_015668.3 S238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr8:101065077 G>C maps to NM_015668.3 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr8:101076155 T>C maps to NM_015668.3 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr8:101020668 A>G maps to NM_015668.3 Y765Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr8:101008722 T>C maps to NM_015668.3 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr8:101016293 T>C maps to NM_015668.3 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr9:116226093 C>A maps to NM_017790.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr1:163043312 C>T maps to NM_001102445.2 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:163117197 G>A maps to NM_003617.3 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr14:73002910 G>A maps to NM_004296.4 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr1:240969619 C>T maps to ENST00000407727 W363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr1:241099948 G>C maps to ENST00000407727 S95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr1:182617313 A>G maps to NM_033345.2 H124H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr17:63173908 C>G maps to NM_003835.3 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:63156420 C>G maps to NM_003835.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:63204068 G>A maps to NM_003835.3 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr17:63221385 G>A maps to NM_003835.3 E558E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:63156667 G>A maps to NM_003835.3 W109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr17:63221274 C>T maps to NM_003835.3 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr17:63200394 C>A maps to NM_003835.3 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr19:33167231 C>T maps to NM_207391.2 H21H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr19:33167864 G>A maps to NM_207391.2 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr6:49582515 C>A maps to NM_000324.2 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr2:227732027 C>A maps to NM_001167608.1 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:109025 C>T maps to NM_022450.3 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr16:114986 C>T maps to NM_022450.3 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr17:74469920 C>T maps to NM_024599.5 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr17:74470534 G>A maps to NM_024599.5 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr17:74467777 G>A maps to NM_024599.5 L836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr17:74470868 A>G maps to NM_024599.5 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:726496 G>A maps to NM_003961.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:39352268 C>T maps to ENST00000372985 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:156354597 G>A maps to NM_020407.3 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr1:25717407 T>C did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:25717356 C>A maps to NM_020485.4 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr15:90026312 G>A maps to NM_016321.1 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr15:90020319 G>A maps to NM_016321.1 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr15:90020800 G>A maps to NM_016321.1 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr1:25599097 G>A maps to ENST00000357542 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:25599109 C>T maps to ENST00000357542 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr7:151181845 G>A maps to NM_005614.3 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:49462821 C>T maps to NM_144593.1 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr3:129247680 G>A maps to NM_000539.3 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr3:129247848 C>T maps to NM_000539.3 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:49397642 C>T maps to NM_001664.2 *194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr10:62637762 G>C maps to NM_014836.4 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr10:62645941 C>T maps to NM_014836.4 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr10:62634777 C>T maps to NM_014836.4 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr8:22862929 C>T maps to NM_001160036.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr8:22864633 C>T maps to NM_001160036.1 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr5:95124487 C>G maps to NM_014899.3 S549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr5:95091438 C>G maps to NM_014899.3 S341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr1:113244329 G>A maps to NM_175744.4 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr11:66837939 C>T maps to NM_014578.3 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BS-01A-21D-A26M-08 chr11:66837936 C>T maps to NM_014578.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:40245011 G>C maps to NM_004310.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr14:63671661 G>A maps to NM_020663.3 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr14:63747705 G>A maps to NM_020663.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:46803240 C>T maps to NM_012249.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:46770262 C>T maps to NM_012249.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:30510206 G>A maps to NM_001033568.1 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr17:30533947 C>A maps to NM_001033568.1 S479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr17:30528025 A>G maps to NM_001033568.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr16:723542 C>T maps to NM_138769.1 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr16:721201 C>T maps to NM_138769.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr16:722084 C>T maps to NM_138769.1 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:228879342 C>T maps to NM_021205.4 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:41165558 C>T maps to NM_133639.3 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr15:41165270 G>A maps to NM_133639.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:119249494 A>T did not map to a codon.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr23:119249647 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:119293111 G>T did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:119210890 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:144463987 G>A maps to ENST00000422773 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr8:144461996 A>G did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:33490609 C>T maps to NM_033103.4 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:33493180 G>A maps to NM_033103.4 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:53454998 G>T did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:45818176 C>T maps to NM_015653.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr22:45813509 C>T maps to NM_015653.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:8132429 C>A maps to ENST00000309737 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:209945 C>T maps to NM_021932.4 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr11:208893 G>T maps to NM_021932.4 E14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:107237643 A>G maps to ENST00000392837 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:12888104 C>T maps to NM_014859.4 R733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:12860052 C>T maps to NM_014859.4 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr5:38952312 C>A maps to ENST00000296782 E1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr5:38955779 C>T maps to ENST00000296782 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr5:38947494 C>T maps to ENST00000296782 L1419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr5:38963046 C>T maps to ENST00000296782 Q499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr5:38982073 G>A maps to ENST00000296782 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr2:152279481 C>T maps to NM_018151.4 Q238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:152330583 C>G maps to NM_018151.4 S2401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:152320266 G>A maps to NM_018151.4 Q1411Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr12:123907607 C>T maps to NM_145058.1 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr12:130919302 C>T maps to NM_015347.4 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr12:130897187 G>A maps to NM_015347.4 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr12:130926566 C>A maps to NM_015347.4 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:130919335 G>A maps to NM_015347.4 F715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr12:130934767 G>A maps to NM_015347.4 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr12:130927065 C>T maps to NM_015347.4 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr12:130923032 G>A maps to NM_015347.4 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr12:130919365 G>A maps to NM_015347.4 D705D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:130927095 G>A maps to NM_015347.4 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:130884301 A>C maps to NM_015347.4 P1018P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr12:130912765 C>T maps to NM_015347.4 G773G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:20458034 C>T maps to NM_015672.1 P1089P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr22:20458067 G>A maps to NM_015672.1 F1078F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr22:20458115 C>G maps to NM_015672.1 R1062R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:42870199 C>G maps to NM_173642.3 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr12:8866635 G>A maps to NM_020734.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr12:8926378 G>C maps to NM_020734.2 *387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr6:72957746 G>T maps to NM_014989.4 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:72957811 C>T maps to NM_014989.4 V741V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:73110295 C>T maps to NM_014989.4 I1653I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr6:73110199 G>C maps to NM_014989.4 V1621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr6:72678706 G>A maps to NM_014989.4 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr6:72806798 C>G maps to NM_014989.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr8:104898275 C>G maps to NM_001100117.2 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr8:104898249 G>T maps to NM_001100117.2 E475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr8:104898392 G>A maps to NM_001100117.2 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr8:104898095 T>C maps to NM_001100117.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr8:104897673 C>T maps to NM_001100117.2 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr8:104898001 C>G maps to NM_001100117.2 S392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr8:104897638 C>G maps to NM_001100117.2 S271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr8:105026784 C>T maps to NM_001100117.2 V1092V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr8:105263828 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:41095024 G>A maps to NM_014747.2 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr1:41107540 C>T maps to NM_014747.2 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr20:43385640 G>A maps to NM_182970.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:66100866 C>T maps to NM_004292.2 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr11:66102402 C>T maps to NM_004292.2 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr20:19955571 G>T maps to ENST00000255006 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr20:19956180 C>T maps to ENST00000255006 F553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr20:19956144 C>T maps to ENST00000255006 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr14:93119202 G>A maps to NM_024832.3 K603K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr14:93125803 C>T maps to NM_024832.3 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr14:93043703 G>C did not map to a codon.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr14:93125803 C>G maps to NM_024832.3 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr14:93119349 G>A maps to NM_024832.3 K652K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr6:33179193 C>T maps to NM_002931.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr6:33179041 C>G maps to NM_002931.3 S188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:39361467 C>A maps to NM_001195833.1 E256*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FD-A6TG-01A-11D-A32B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr7:105190499 A>G did not map to a codon.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr7:105205876 G>A maps to NM_021930.4 E680E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr6:7404770 C>T maps to NM_031480.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr18:21057016 C>T maps to NM_003831.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr6:3083473 C>A maps to NM_003804.3 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr8:90784893 G>T did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr14:24808328 C>T maps to NM_006871.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr14:24806654 G>A maps to NM_006871.3 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr21:43161780 C>T maps to ENST00000352483 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr21:43161771 G>A maps to ENST00000352483 N575N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr21:43161998 C>A maps to ENST00000352483 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr21:43187135 G>A maps to ENST00000352483 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr21:43162128 C>T maps to ENST00000352483 K456K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr23:106144120 G>A did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr18:40323574 C>T maps to NM_002930.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr18:40613805 G>A maps to NM_002930.2 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr15:89760378 G>A maps to NM_000326.4 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr15:89760486 C>T maps to NM_000326.4 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr15:89760438 C>T maps to NM_000326.4 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:40701822 A>G maps to NM_012421.3 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:40627070 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:40703420 C>G maps to NM_012421.3 S1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:40697308 C>T maps to NM_012421.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:40703681 C>G maps to NM_012421.3 S1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:40704840 G>A maps to NM_012421.3 R1489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:40668209 C>G maps to NM_012421.3 S245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr23:73812091 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:73812834 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr23:73814149 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr23:73811690 C>T did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr23:73812255 T>C did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr23:73811937 G>C did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:73812515 T>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:73812516 T>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr23:73812301 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:73811493 C>G did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr9:5304390 G>A maps to NM_134441.1 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr16:67682818 G>A maps to NM_001013838.1 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr16:67685193 C>T maps to NM_001013838.1 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:67683402 C>T maps to NM_001013838.1 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr16:67681503 A>T maps to NM_001013838.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr16:67682982 C>T maps to NM_001013838.1 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr16:67683015 C>A maps to NM_001013838.1 I543I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr16:67683402 C>T maps to NM_001013838.1 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr16:67683408 C>T maps to NM_001013838.1 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr16:67686427 C>A maps to NM_001013838.1 V957V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr16:67685872 C>T maps to NM_001013838.1 Q880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:86615972 G>A maps to NM_024945.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:151742432 C>T maps to NM_017909.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr6:151757628 G>A maps to NM_017909.2 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr5:177573137 C>T maps to NM_022762.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr5:177574630 T>C maps to NM_022762.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr5:177570948 C>T maps to NM_022762.3 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:20978928 C>G maps to ENST00000430083 S128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr14:21052597 G>A maps to NM_145250.3 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr14:21502225 C>T maps to NM_001012264.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr14:21359943 G>T maps to NM_002935.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr14:21360168 C>T maps to NM_002935.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr14:21025033 G>A maps to NM_001110361.1 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr14:21024719 C>T maps to NM_001110361.1 W175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr1:182551219 C>T maps to NM_021133.3 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr5:31526613 G>A maps to NM_013235.4 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr5:31526848 G>C maps to NM_013235.4 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr5:31526190 C>G maps to NM_013235.4 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr6:167343132 C>G maps to ENST00000428859 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr6:167352456 C>T maps to ENST00000428859 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr12:49251877 G>A maps to NM_014470.3 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr12:49251974 G>C maps to NM_014470.3 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:120995411 G>A maps to ENST00000458409 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:120995452 G>A maps to ENST00000458409 W312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr12:120990432 T>C maps to ENST00000458409 H162H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:120995396 G>A maps to ENST00000458409 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr12:120995452 G>A maps to ENST00000458409 W312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr2:86832095 G>A maps to NM_005667.3 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:86832070 G>C maps to NM_005667.3 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:51736895 C>T maps to NM_014372.4 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr15:59358968 C>G maps to ENST00000434298 S458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr15:59323898 C>G maps to ENST00000434298 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr15:59376406 C>T maps to ENST00000434298 Q802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr15:59381908 C>G maps to ENST00000434298 S874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr15:59368278 C>T maps to ENST00000434298 Q605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:19316426 C>T maps to NM_007148.4 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:19316616 A>C maps to NM_007148.4 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:19316420 C>T maps to NM_007148.4 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr17:19318605 C>G maps to NM_007148.4 S435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr17:19319164 G>T maps to NM_007148.4 E525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr17:19319265 C>A maps to NM_007148.4 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr23:119005262 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr13:98828974 C>T maps to NM_178861.4 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:48562720 G>A maps to NM_018683.3 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:145688150 G>A maps to NM_014455.2 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:145682085 T>C maps to NM_014455.2 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:71698133 C>T maps to NM_018320.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr11:71698076 C>T maps to NM_018320.4 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr8:33408567 T>C maps to NM_024787.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr3:49728873 G>A maps to NM_022064.2 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr3:49739786 C>T maps to NM_022064.2 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr3:49753086 C>T maps to NM_022064.2 L1030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr3:49758231 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr3:49743428 C>T maps to NM_022064.2 S773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr3:49735548 C>T maps to NM_022064.2 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr3:49736207 C>T maps to NM_022064.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr3:49750027 C>T maps to NM_022064.2 I871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:49758046 C>T maps to NM_022064.2 L1202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr3:49737990 C>T maps to NM_022064.2 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr18:29617111 G>A maps to NM_017831.3 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr18:29617077 G>T did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:651660 G>A maps to ENST00000340092 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:651726 C>T maps to ENST00000340092 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr23:106016179 G>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr23:106016352 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:105937495 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr23:106034370 G>A did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr23:106038817 C>G did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:105970541 T>C did not map to a codon.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr3:149619892 C>T maps to NM_007282.4 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr7:122338240 C>T maps to NM_139175.1 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr17:29325725 G>A maps to NM_032322.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr17:29311733 C>T maps to NM_032322.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr17:29311675 G>A maps to NM_032322.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr18:29704793 C>T maps to NM_001191324.1 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:125487427 C>G maps to NM_007218.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:125487526 C>G maps to NM_007218.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:125487415 C>G maps to NM_007218.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr8:125487358 C>T maps to NM_007218.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:141358011 C>T maps to NM_183399.1 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr5:141358301 G>A maps to NM_183399.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr5:141358301 G>A maps to NM_183399.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr2:7137189 C>T maps to NM_014746.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr5:158590023 A>T maps to NM_144726.2 Y423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr5:158603708 G>C maps to NM_144726.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr5:158588321 C>T maps to NM_144726.2 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr5:158630532 G>A maps to NM_144726.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:158630580 C>T maps to NM_144726.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr7:122341898 G>A maps to NM_198085.1 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr7:122342072 G>C maps to NM_198085.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:122342213 G>A maps to NM_198085.1 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr2:101893732 C>T maps to NM_173647.3 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr2:101924810 C>A maps to NM_173647.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr4:141888842 G>T maps to NM_020724.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr4:141789489 C>T maps to NM_020724.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr18:59483504 G>A maps to NM_173557.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:74148487 G>A maps to NM_052916.2 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr17:74169826 C>T maps to NM_052916.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:74158007 G>A maps to NM_052916.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr17:74151720 G>A maps to NM_052916.2 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr21:30307436 G>T maps to NM_015565.2 G1669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr21:30307607 T>C maps to NM_015565.2 S1612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr16:88767738 C>T maps to NM_178841.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr3:196199274 C>T maps to NM_152617.3 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr3:196198863 T>A maps to NM_152617.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr3:196210762 C>G did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:196199400 G>C maps to NM_152617.3 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr3:196198908 G>A maps to NM_152617.3 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr3:196198864 G>C maps to NM_152617.3 S514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr11:74459942 G>A maps to NM_001098638.1 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr11:74547712 C>A maps to NM_001098638.1 R689R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr11:74546754 T>C maps to NM_001098638.1 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr11:74546844 C>T maps to NM_001098638.1 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:25453350 A>G maps to ENST00000381927 T1649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr13:25370419 C>T maps to ENST00000381927 D462D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr13:25367380 G>A maps to ENST00000381927 Q379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr13:25399908 C>T maps to ENST00000381927 I748I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr13:25448249 A>G did not map to a codon.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr13:25399839 C>G maps to ENST00000381927 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr8:42711505 G>A maps to NM_030954.3 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr4:154669823 C>T maps to ENST00000274068 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr4:154636766 G>A maps to ENST00000274068 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:63510307 G>A maps to NM_001113561.1 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr5:63509791 G>A maps to NM_001113561.1 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:85823746 G>A maps to NM_016494.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr2:85823765 C>T maps to NM_016494.3 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:85824036 C>T maps to NM_016494.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:20141393 C>T maps to NM_019062.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr8:101270980 G>A maps to NM_183419.1 Q774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr8:101271435 G>C maps to NM_183419.1 S622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:185056734 G>A maps to NM_007212.3 W17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:185056769 C>T maps to NM_007212.3 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr9:104314696 G>A maps to NM_019592.5 Q521Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr9:104309796 G>A maps to NM_019592.5 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr9:104302627 G>A maps to NM_019592.5 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr9:104302806 T>A maps to NM_019592.5 Y111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr9:104303102 C>T maps to NM_019592.5 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:6272367 C>T maps to NM_207396.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:6270485 G>C maps to NM_207396.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr1:6279391 G>A maps to NM_207396.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:140115103 G>C maps to NM_031297.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:140115580 G>T maps to NM_031297.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr17:78350114 G>A maps to NM_020914.4 V4449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr17:78262065 C>T maps to NM_020914.4 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:78353430 G>A maps to NM_020914.4 P4568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:78343328 C>T maps to NM_020914.4 F4110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr17:78293138 G>A maps to NM_020954.2 T1017T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr17:78293101 C>G maps to NM_020914.4 S1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr17:78318807 C>T maps to NM_020914.4 Q2274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:78328355 C>G maps to NM_020914.4 L3663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr17:78317760 C>T maps to NM_020914.4 I2145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr17:78362989 G>A maps to NM_020914.4 S5055S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr17:78314023 C>T maps to NM_020914.4 Q2002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr17:78321833 C>T maps to NM_020914.4 V3282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:78314034 C>T maps to NM_020914.4 L2005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr17:78335676 G>T maps to NM_020914.4 E3831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr17:78320893 C>G maps to NM_020914.4 S2969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr17:78319815 C>T maps to NM_020914.4 L2610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:78263540 C>G maps to NM_020914.4 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr17:78367147 G>A maps to NM_020914.4 L5207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr17:78324136 C>T maps to NM_020914.4 L3424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr17:78354693 G>A maps to NM_020914.4 V4617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr22:30776327 G>A maps to NM_001017981.1 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr7:5680958 C>T maps to NM_207111.2 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr7:5751424 C>T maps to NM_207111.2 K676K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr7:5781383 C>G maps to NM_207111.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr7:5792610 C>G did not map to a codon.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr7:5781362 C>T maps to NM_207111.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr7:5780798 C>G maps to NM_207111.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr7:5780603 C>A maps to NM_207111.2 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr6:125379251 G>A maps to NM_152553.2 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr13:79219060 A>G maps to NM_024546.3 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr13:79190192 G>C maps to NM_024546.3 S568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr13:79233215 G>A maps to NM_024546.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr13:79190636 G>C maps to NM_024546.3 S420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:45115331 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr1:44878060 C>T maps to ENST00000453887 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:219530893 G>A maps to NM_022453.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:219532975 G>A maps to NM_022453.2 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:219532975 G>A maps to NM_022453.2 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:219529466 G>A maps to NM_022453.2 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:24617579 G>A maps to NM_017999.4 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr14:24616999 G>A maps to NM_017999.4 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr14:24619593 G>A maps to NM_017999.4 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr12:121855572 G>T maps to NM_194271.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:36375991 G>A maps to NM_022781.4 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr6:30043545 C>G maps to NM_025236.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr6:30043391 C>A maps to NM_025236.3 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr16:30785257 G>A did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:30777494 G>A maps to NM_014771.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:30783275 C>T maps to NM_014771.2 F903F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:30776274 C>G maps to NM_014771.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:30780184 G>A maps to NM_014771.2 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr16:30778106 C>T maps to NM_014771.2 Q447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr16:30779605 G>A maps to NM_014771.2 K578K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr12:56601469 G>A maps to NM_194359.1 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:175958583 C>T maps to NM_014901.4 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr5:175958609 G>A maps to NM_014901.4 L107L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-4Z-AA7R-01A-11D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr6:32148013 C>T maps to NM_006913.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:32147489 G>A maps to NM_006913.3 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr13:26789664 C>T maps to NM_005977.3 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr13:26788722 G>A maps to NM_005977.3 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:141457241 C>G maps to NM_014245.3 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:37336787 C>T maps to NM_003958.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:37358521 G>A maps to NM_003958.3 K482K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr17:58040311 G>A maps to NM_016125.3 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:58030412 G>T maps to NM_016125.3 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr12:117204651 C>T maps to NM_001109903.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr6:89388139 T>C did not map to a codon.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr6:89554234 C>T maps to NM_003800.3 Q370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr6:89479548 A>G maps to NM_003800.3 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:498608 G>A maps to NM_203389.1 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:494696 G>A maps to NM_203389.1 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr11:499016 G>C maps to NM_203389.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr10:90342887 C>T maps to NM_001031709.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr10:90332801 G>A maps to NM_001031709.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:90342932 C>G maps to NM_001031709.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr10:90122396 C>T maps to NM_001031709.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr10:90074273 C>T maps to NM_001031709.2 P275P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-4Z-AA81-01A-11D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr17:685882 G>T maps to NM_018146.2 E89*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ZF-A9RF-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr1:201965364 G>A maps to NM_020216.3 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr2:241514465 G>T maps to NM_018226.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr2:241513628 C>T maps to NM_018226.3 F115F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BT-A42B-01A-32D-A23M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr16:2304012 C>T maps to ENST00000454671 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr16:2314626 C>A maps to NM_080594.2 V6V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-E7-A3Y1-01A-11D-A22Z-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr16:2305695 G>A maps to ENST00000454671 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:156025191 C>G maps to NM_014017.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:156025059 G>A maps to NM_014017.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr3:78685191 G>C maps to NM_002941.3 S1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:78649351 C>A maps to NM_002941.3 E1618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr3:78688942 C>T maps to NM_002941.3 T996T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr3:78695329 C>T maps to NM_002941.3 Q950Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr3:78700966 G>A maps to NM_002941.3 I909I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr3:78706262 G>A maps to NM_002941.3 Q867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr3:77651382 C>A maps to ENST00000332191 G959G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr3:77614212 G>A maps to ENST00000332191 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:77666772 C>T maps to ENST00000332191 R1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:77684100 C>T maps to ENST00000332191 Q1342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr3:77657031 C>T maps to ENST00000332191 L1074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:77638058 G>A maps to ENST00000332191 K886K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr3:77623777 C>T maps to ENST00000332191 V700V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:77611800 G>A did not map to a codon.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr3:77671444 T>C maps to ENST00000332191 L1208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:77147264 G>C maps to ENST00000332191 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:77600135 T>A maps to ENST00000332191 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr3:77651409 C>T maps to ENST00000332191 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr11:124740559 G>A maps to NM_022370.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:124747959 A>G maps to NM_022370.3 Q1038Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr11:124755143 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:124757736 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr11:124763843 G>C maps to NM_019055.5 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr11:124761613 G>A maps to NM_019055.5 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr18:18622099 G>C maps to NM_005406.2 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr18:18546938 G>A maps to NM_005406.2 L1097L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr2:11367378 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:11361430 G>A maps to NM_004850.3 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:11338882 C>T maps to NM_004850.3 R976R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr9:114993694 T>G did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr9:115030430 C>T maps to NM_001163790.1 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr9:114986146 G>C maps to NM_001163790.1 S551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr16:4848113 G>T maps to NM_024589.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr16:4847735 G>C maps to NM_024589.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr11:62381882 C>G maps to NM_000327.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr3:123688012 G>A maps to NM_017578.2 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:123699229 G>A maps to NM_017578.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr3:125701189 C>T maps to NM_001012337.1 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr5:10461435 G>A maps to NM_031916.3 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr5:10442378 C>T maps to NM_031916.3 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:64643838 G>A maps to NM_005012.2 V705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:64643415 C>T maps to NM_005012.2 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr1:64643245 T>C maps to NM_005012.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr1:64605961 C>T maps to NM_005012.2 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr1:64608151 G>A maps to NM_005012.2 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr9:94486309 G>A maps to NM_004560.2 N822N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:94486309 G>A maps to NM_004560.2 N822N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:94493357 C>T maps to NM_004560.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr9:94487116 G>A maps to NM_004560.2 F553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr9:94486757 G>C maps to NM_004560.2 S673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr9:94495617 C>A maps to NM_004560.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr9:94495506 G>A maps to NM_004560.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:60789728 C>T maps to NM_134260.2 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr15:60803788 C>T maps to NM_134260.2 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr9:77286711 C>A maps to ENST00000396204 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr9:77249650 A>G maps to ENST00000396204 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:151801934 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:151785507 G>T maps to ENST00000392697 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr6:117631383 C>A maps to NM_002944.2 V2098V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr6:117746801 A>G maps to NM_002944.2 C6C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr6:117710843 G>A maps to NM_002944.2 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr6:117645492 A>C did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:55533795 C>T maps to NM_006269.1 H90H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:55538470 C>T maps to NM_006269.1 R677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr8:55542216 C>T maps to NM_006269.1 I1925I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr8:55538470 C>T maps to NM_006269.1 R677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr8:55538694 C>A maps to NM_006269.1 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr8:55540137 C>T maps to NM_006269.1 I1232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr8:55538162 C>G maps to NM_006269.1 S574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:10468838 G>A maps to NM_178857.5 S923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:10467251 C>T maps to NM_178857.5 E1452E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr8:10473956 G>A maps to NM_178857.5 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr8:10466759 G>A maps to NM_178857.5 L1616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr8:10480435 G>A maps to NM_178857.5 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr8:10468646 C>G maps to NM_178857.5 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr8:10465495 C>A maps to NM_178857.5 E2038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr8:10470785 C>T maps to NM_178857.5 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:46712996 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:46713215 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr7:33136130 G>A maps to NM_203288.1 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:1747275 A>T maps to NM_002945.3 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:1780583 C>T maps to NM_002945.3 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr17:1795167 T>C maps to NM_002945.3 C531C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr7:7678738 C>A maps to NM_002947.3 G46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr23:96139473 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:96139911 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:96139570 A>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr23:96139743 T>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr15:41820132 C>T maps to NM_015540.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr15:41814012 C>T maps to NM_015540.2 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr15:41813023 G>C maps to NM_015540.2 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr1:92789859 G>C maps to NM_024813.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:92846349 C>T maps to NM_024813.2 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr1:92772768 C>T maps to NM_024813.2 Q142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr12:48084422 C>G did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:68904996 C>T maps to NM_000329.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:84961960 C>T maps to NM_025065.6 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr1:84944969 G>T maps to NM_025065.6 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:111306251 G>T maps to NM_032194.1 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr23:38182777 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr23:38150240 A>C did not map to a codon.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr23:38156596 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr23:38147248 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr23:38156637 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr23:38128982 T>G did not map to a codon.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr23:38158325 T>C did not map to a codon.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr23:38134399 C>G did not map to a codon.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr23:38147257 C>T did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr23:38135985 C>G did not map to a codon.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr23:38146432 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr23:38128878 T>C did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:38146395 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr14:21788312 T>C maps to NM_020366.3 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr14:21780020 C>G maps to NM_020366.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr16:53679567 C>T maps to NM_015272.2 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr16:53726196 G>A maps to NM_015272.2 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr16:53720412 C>T maps to NM_015272.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr16:53726178 C>A maps to NM_015272.2 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr16:53726239 C>T maps to NM_015272.2 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:113304638 G>A maps to NM_001143854.1 Q146Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr12:113303254 C>T maps to NM_001143854.1 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr12:113266186 C>T maps to NM_001143854.1 Q22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr12:113325676 G>A maps to NM_001143854.1 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:113314468 G>A maps to NM_001143854.1 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr12:113314630 G>A maps to NM_001143854.1 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr2:89037504 G>C maps to NM_144563.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:153629108 G>A did not map to a codon.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr23:153627863 A>G did not map to a codon.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr23:153629056 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr6:35438388 G>A maps to NM_007104.4 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr14:47120528 G>C maps to NM_080746.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr14:47120420 G>A maps to NM_080746.2 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr14:47120593 G>A maps to NM_080746.2 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:24021181 C>T maps to NM_000975.3 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr1:24020390 G>A maps to NM_000975.3 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr1:24020312 A>G maps to NM_000975.3 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr9:130210619 G>C maps to NM_000976.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr16:89629386 C>G maps to NM_033251.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:40500161 G>A maps to NM_001034996.1 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:49119426 G>A maps to NM_000979.2 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:49120575 C>T maps to NM_000979.2 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:49118688 G>C maps to NM_000979.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr19:17972199 C>A maps to NM_000980.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr17:37008911 C>A maps to NM_000978.3 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr3:101400023 C>A maps to NM_000986.3 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr3:101404751 C>T maps to NM_000986.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:172386932 C>T maps to NM_016093.2 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:172386962 C>T maps to NM_016093.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:39708980 C>T maps to NM_000967.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:39710726 C>T maps to NM_000967.3 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr22:39713470 C>T maps to NM_000967.3 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr2:101620641 C>A maps to NM_000993.4 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:12877706 C>T maps to ENST00000273223 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:127623765 C>T maps to NM_007209.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr19:5691352 C>T maps to NM_015414.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr5:40834705 C>T maps to NM_000997.4 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr16:1995613 G>C maps to NM_005061.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr1:93300334 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr1:93301833 C>T maps to NM_000969.3 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr12:112843710 C>T maps to NM_001024662.1 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr8:74204108 C>T maps to ENST00000396470 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr9:136216478 G>A maps to NM_000972.2 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr6:42851228 C>A maps to NM_198486.2 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:39456162 T>G maps to NM_000661.4 *193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr15:69746005 C>T maps to NM_001003.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:69746005 C>G maps to NM_001003.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:810263 T>C maps to NM_001004.3 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr3:128356704 G>A maps to NM_002950.3 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr3:128356736 G>A maps to NM_002950.3 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr20:35835680 G>A maps to NM_002951.3 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr20:35865106 C>G maps to NM_002951.3 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr20:35866819 G>A maps to NM_001135771.1 Q601Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr20:35860768 C>A maps to NM_002951.3 S551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:58296275 C>T maps to NM_007042.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr6:30314534 C>G maps to ENST00000412529 S399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr15:75248519 G>A maps to NM_017793.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr15:75248615 G>C maps to NM_017793.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr18:33607164 G>A maps to NM_018170.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr20:36662387 C>T maps to NM_021215.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr20:36662411 G>A maps to NM_021215.3 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr20:36668882 C>T maps to NM_021215.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:150443791 C>T maps to NM_015203.3 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:150337363 C>T maps to NM_015203.3 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr1:150444714 G>A maps to NM_015203.3 R1097R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:150444195 G>T maps to NM_015203.3 G924G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr1:150418852 C>A maps to NM_015203.3 Y282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:150445618 T>C maps to NM_015203.3 L1399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr2:154334878 G>A maps to NM_019845.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:154334836 G>T maps to NM_019845.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:45056166 C>T maps to NM_203400.3 Q69Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:45056118 G>A maps to NM_203400.3 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:45056118 G>A maps to NM_203400.3 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr17:45056103 G>A maps to NM_203400.3 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr11:17098722 G>T maps to NM_001017.2 S48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:1440119 G>A maps to NM_001018.3 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:39926339 C>T maps to NM_001020.4 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr6:33243656 T>C maps to NM_022551.2 D62D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:42373787 C>T maps to NM_001022.3 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr22:39925616 C>T maps to NM_194326.2 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr22:39928409 C>T maps to NM_194326.2 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr16:2012181 G>A maps to NM_002952.3 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr16:2012570 C>T maps to NM_002952.3 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:2012817 G>A maps to NM_002952.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr16:2014321 C>T maps to NM_002952.3 K74K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr8:56986682 C>T maps to NM_001146227.1 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr8:56986655 G>A maps to NM_001146227.1 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr8:56986286 G>A maps to NM_001146227.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:153964054 C>T maps to NM_001030.4 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:8386541 C>T maps to NM_001031.4 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr23:71495438 C>T did not map to a codon.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr23:71493143 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:71494971 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:71494973 C>G did not map to a codon.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr23:71493767 G>A did not map to a codon.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr23:71495425 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr24:2722722 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr24:22918663 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:19376563 C>G maps to NM_001010.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr9:19376293 T>C maps to NM_001010.2 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:26898055 G>T maps to NM_001006665.1 G578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr6:166845909 C>T maps to ENST00000510118 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr6:166836797 C>T maps to ENST00000510118 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:166844057 C>T maps to ENST00000510118 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr6:166944801 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr6:166836851 C>T maps to ENST00000510118 G570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr23:20194391 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:20252920 T>G did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr23:20190949 C>A did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:20205974 C>T did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr23:20183018 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:20195167 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr23:20212355 A>G did not map to a codon.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr11:64136985 G>T maps to NM_003942.2 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr11:64129187 C>T maps to NM_003942.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr14:91356956 C>T maps to NM_004755.2 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr14:91526742 C>T maps to NM_004755.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr14:91356875 G>A maps to NM_004755.2 N597N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr23:83442828 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr23:83352850 A>G did not map to a codon.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr23:83361947 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:83361412 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr23:83351236 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr23:83362044 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr23:83360853 C>T did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:83375019 T>C did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:83359637 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:83320047 T>G did not map to a codon.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr23:83320117 T>C did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr23:83361430 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr23:83372136 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:83419373 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:58013629 G>T maps to NM_003161.2 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:58022808 G>T maps to NM_003161.2 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:58003875 C>T maps to NM_003161.2 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr11:67198960 C>G maps to NM_003952.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr11:67200435 G>C maps to NM_003952.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:67202102 C>T maps to NM_003952.2 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr11:67200836 G>A maps to NM_003952.2 K275K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr1:213436149 C>G maps to NM_012424.3 L1027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr1:213415602 C>T maps to NM_012424.3 R928R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr2:3627747 C>T maps to NM_001011.3 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr2:3627711 A>T maps to NM_001011.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr1:45242393 G>A maps to NM_001012.1 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:152128073 G>A maps to NM_001122965.1 Q501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr1:152128361 G>A maps to NM_001122965.1 Q405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr1:152129394 G>C maps to NM_001122965.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr1:152130233 G>T maps to NM_001122965.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr17:78796045 G>A maps to NM_020761.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr17:78936368 G>C maps to NM_020761.2 L1267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr17:78704397 G>A maps to NM_020761.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr17:78897445 G>T maps to NM_020761.2 R927R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr17:78865581 C>A maps to NM_020761.2 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr17:78923267 G>A maps to NM_020761.2 K1097K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:78865557 T>A maps to NM_020761.2 Y674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr3:9885242 G>C maps to NM_173659.3 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:219449361 A>G maps to NM_005444.1 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr23:55784743 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr23:55777614 G>T did not map to a codon.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr23:55784733 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:55757804 C>T did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr6:90090014 G>A maps to NM_021244.4 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr6:90087532 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:50139971 C>A maps to NM_006270.3 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr19:50139031 G>C maps to NM_006270.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr20:17596588 G>C maps to ENST00000377813 L1311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr20:17602400 C>A maps to ENST00000377813 L1086L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr20:17606165 C>T maps to ENST00000377813 V1015V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:7231403 C>T maps to NM_001003699.3 V1024V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr6:7229535 C>T maps to NM_001003699.3 Q402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr6:7231958 C>T maps to NM_001003699.3 A1209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr6:7211054 G>A maps to NM_001003699.3 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:7229526 C>T maps to NM_001003699.3 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:7230392 C>T maps to NM_001003699.3 I687I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr6:7230401 G>T maps to NM_001003699.3 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:7248825 G>A maps to NM_001003699.3 Q1618Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:7229505 C>T maps to NM_001003699.3 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr6:7229780 G>A maps to NM_001003699.3 Q483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:7229535 C>T maps to NM_001003699.3 Q402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr6:7229505 C>T maps to NM_001003699.3 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr6:7230629 T>C maps to NM_001003699.3 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr4:110763651 C>T maps to NM_006583.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:110756604 C>T maps to NM_006583.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr11:4123241 C>T maps to NM_001033.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:10263126 G>A maps to NM_001165931.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr8:103236280 A>G maps to NM_015713.4 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr8:103238199 G>A maps to NM_015713.4 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr16:15155702 G>A maps to NM_018427.3 T618T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr16:15166893 C>G maps to NM_018427.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:45212581 C>T maps to NM_003683.5 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr10:99133482 G>A maps to NM_015179.3 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:99123622 C>T maps to NM_015179.3 V1185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr10:99160976 C>T maps to NM_015179.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:99139128 G>A maps to NM_015179.3 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr10:99133437 G>A maps to NM_015179.3 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:218478401 C>T maps to NM_016052.3 C146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:218458680 C>G maps to NM_016052.3 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:218458742 G>T maps to NM_016052.3 G29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:218478380 G>A maps to NM_016052.3 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr21:45104495 C>T maps to NM_015056.2 H318H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr21:45107623 G>T maps to NM_015056.2 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr21:45107562 G>T maps to NM_015056.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr21:45107562 G>T maps to NM_015056.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr21:45113164 G>C maps to NM_015056.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr22:42910192 G>A maps to NM_015703.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr22:42914106 G>C maps to NM_015703.4 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:6622488 G>C maps to NM_015324.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr11:6621802 C>T maps to NM_015324.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr3:51971683 C>T did not map to a codon.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr3:51968529 C>T maps to NM_004704.3 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr3:51967776 G>A maps to NM_004704.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr8:67341395 C>T maps to NM_015169.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr23:18675761 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr17:48559780 C>T maps to NM_018346.1 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr1:114308927 A>G maps to NM_018364.3 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr7:77325842 C>T maps to NM_198467.2 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:77326034 C>G maps to NM_198467.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr7:77379115 C>A maps to NM_198467.2 S360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr7:77379116 G>T maps to NM_198467.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:15987792 C>A maps to NM_006511.1 S477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:15986461 C>G maps to NM_006511.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:15987252 C>A maps to NM_006511.1 S297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:15987284 C>T maps to NM_006511.1 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:15988047 C>G maps to NM_006511.1 S562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr1:15986518 T>C maps to NM_006511.1 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr11:77412857 A>G maps to NM_016578.3 Y472Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr16:11931706 C>G maps to NM_015659.2 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr21:43916271 A>G maps to NM_080860.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:5983621 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr6:159404768 C>T maps to NM_031924.4 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr6:116949360 C>T maps to NM_001010892.2 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr6:116938177 C>A maps to NM_001010892.2 S131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr19:46307815 G>A maps to NM_030785.3 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr19:46317932 T>G maps to NM_030785.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr19:46308268 C>T maps to NM_030785.3 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:46303816 G>A maps to NM_030785.3 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr8:108970469 C>A maps to NM_178565.4 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr8:108972968 A>G maps to NM_178565.4 H120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr8:108970401 C>T maps to NM_178565.4 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:947850 G>A maps to NM_001029871.3 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:57250817 G>T maps to NM_133368.1 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr3:157841703 C>T maps to NM_016625.2 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr3:157839928 C>T maps to NM_016625.2 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr12:122999746 C>T maps to NM_023012.5 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr12:122990074 C>T maps to NM_023012.5 *435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr19:12945626 G>T maps to NM_031429.1 S17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:100732129 C>T maps to NM_001130841.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr1:100733738 C>T maps to NM_001130841.1 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:23482514 C>T maps to NM_014433.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr22:23406201 G>T maps to NM_014433.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr22:23406132 G>A maps to NM_014433.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr22:23404080 G>A maps to NM_014433.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr22:23406222 G>A maps to NM_014433.2 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr20:62324556 G>C maps to ENST00000482936 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr20:62324318 C>G maps to ENST00000482936 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr20:62326723 C>A maps to ENST00000482936 I1181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr2:74657091 C>G maps to NM_001015055.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:74654712 G>A maps to NM_001015055.1 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:74657612 C>A maps to NM_001015055.1 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr10:64022430 C>T maps to NM_145307.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BS-01A-21D-A26M-08 chr10:63957666 C>T maps to NM_145307.2 *610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr14:101348374 G>T maps to NM_001134888.2 Y917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr14:101350750 T>C maps to NM_001134888.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:60194327 G>A maps to NM_021136.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr14:60193838 G>T maps to NM_021136.2 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr14:60194248 C>A maps to NM_021136.2 E385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:45996514 G>T maps to NM_005619.3 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:45998200 C>A maps to NM_005619.3 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:63486764 C>G maps to ENST00000377819 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr11:63520560 G>C maps to ENST00000377819 L966L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr11:63487794 G>A maps to ENST00000377819 E607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr11:63525626 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:55252387 G>C maps to NM_020532.4 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr2:55254621 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr2:55252819 G>A maps to NM_020532.4 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr2:55253541 C>A maps to NM_020532.4 E565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:107035676 G>C maps to NM_032730.4 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr22:20229998 C>A maps to ENST00000425986 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr17:1840116 G>A maps to NM_178568.2 H333H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr11:57243960 C>G maps to NM_178570.1 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:57243798 C>T maps to NM_178570.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:57243900 T>A maps to NM_178570.1 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr3:186917785 C>T maps to NM_153708.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:187419766 C>T maps to NM_001004312.2 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:187416546 G>T maps to NM_001004312.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:187416375 G>A maps to NM_001004312.2 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr3:46542024 C>G maps to NM_031440.1 S112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr3:46539567 G>T maps to NM_031440.1 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr3:187088875 C>A maps to NM_022147.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr18:67788893 C>T maps to NM_173630.3 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr18:67687893 G>C maps to NM_173630.3 S2037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr18:67857796 G>C maps to NM_173630.3 S389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr18:67872465 G>A maps to NM_173630.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr18:67673619 C>T maps to NM_173630.3 Q2174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr5:179032921 G>A maps to NM_025158.3 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr5:178977722 G>A maps to NM_025158.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:179018729 G>A maps to NM_025158.3 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr10:70105554 G>C maps to NM_017987.4 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr10:70105550 G>A maps to NM_017987.4 Q634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr10:70156624 G>A maps to NM_017987.4 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr10:70105548 C>T maps to NM_017987.4 Q634Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr4:71634326 G>C maps to NM_001037442.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr4:71630290 C>G maps to NM_001037442.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr4:71630290 C>G maps to NM_001037442.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr4:71640935 G>A maps to NM_001037442.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr2:218947874 G>A maps to NM_198483.3 Q466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:87407140 C>T maps to NM_138290.2 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr8:93017450 G>T maps to NM_175634.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr8:92972520 C>T maps to NM_175634.2 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr8:93027007 G>A maps to NM_175634.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:45405784 A>C maps to ENST00000359524 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr6:45390468 G>A maps to ENST00000359524 Q134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr6:45390447 G>A maps to ENST00000359524 Q127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr1:25229011 C>T maps to NM_001031680.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:155291599 C>A maps to NM_001105203.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr1:155294729 G>A maps to NM_001105203.1 K484K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:155292223 C>T maps to NM_001105203.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:155294699 G>A maps to NM_001105203.1 Q474Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:155291966 C>T maps to NM_001105203.1 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr1:155291599 C>T maps to NM_001105203.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr1:155292043 C>T maps to NM_001105203.1 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:155292067 C>T maps to NM_001105203.1 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:155294965 G>A maps to NM_001105203.1 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:155298022 C>T maps to NM_001105203.1 Q833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr1:155291668 G>A maps to NM_001105203.1 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr1:155292592 C>T maps to NM_001105203.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:127831850 G>A maps to NM_003707.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:127816332 G>A maps to NM_003707.2 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:127801371 C>A maps to NM_003707.2 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:49514295 C>T maps to NM_006666.1 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr19:49507640 C>G maps to NM_006666.1 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr19:49510320 C>T maps to NM_006666.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr19:49513130 C>A maps to NM_006666.1 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:116911481 G>A maps to NM_015952.2 W154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr6:83905758 G>A maps to NM_033411.3 W216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr21:30380856 A>C maps to NM_016940.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr21:30380386 G>A maps to NM_016940.2 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr4:159569648 A>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:159567973 C>T maps to ENST00000440678 F486F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr4:159443178 T>C did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr13:32376281 G>C did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr5:33937087 G>A maps to NM_016568.3 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr5:33937738 C>T maps to NM_016568.3 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr5:33937954 G>A maps to NM_016568.3 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:33937996 C>A maps to NM_016568.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr5:33937234 G>A maps to NM_016568.3 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:155912333 C>T maps to NM_181885.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:155911571 G>A maps to NM_181885.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:155912093 G>A maps to NM_181885.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:155912156 C>T maps to NM_181885.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr9:137300843 G>A maps to NM_002957.4 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr9:137321050 C>T maps to NM_002957.4 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr9:137300142 C>G maps to NM_002957.4 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr9:137328324 C>G maps to NM_002957.4 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr9:137328330 C>G maps to NM_002957.4 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr9:137328448 C>T maps to NM_002957.4 Q460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr9:137300831 C>T maps to NM_002957.4 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:33165596 C>T maps to ENST00000374685 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:33162524 G>A maps to ENST00000374685 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr6:33165551 G>A maps to ENST00000374685 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr6:33168219 G>A maps to ENST00000374685 Q12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:165398041 G>A maps to NM_006917.4 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:133921683 C>T maps to ENST00000296084 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:133910695 C>A maps to ENST00000296084 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr3:133896862 C>A maps to ENST00000296084 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr3:133941282 G>A maps to ENST00000296084 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr3:133878180 G>A maps to ENST00000296084 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr19:39001178 G>T maps to NM_000540.2 E2992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr19:38954076 C>T maps to NM_000540.2 P864P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:39008107 G>A maps to NM_000540.2 E3265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:39061260 G>A maps to NM_000540.2 R4558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr19:38990293 C>T maps to NM_000540.2 N2349N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:39001343 C>G maps to NM_000540.2 L3015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr19:38934383 C>G maps to NM_000540.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr19:38946300 C>G maps to NM_000540.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr19:38951128 C>T maps to NM_000540.2 I825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr19:38986890 G>T maps to NM_000540.2 P2195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr19:39013888 C>G maps to NM_000540.2 V3460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr19:38996585 G>A maps to NM_000540.2 Q2847Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:38973698 C>T maps to NM_000540.2 V1551V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr19:38995513 G>T maps to NM_000540.2 E2732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr19:38949957 C>T maps to NM_000540.2 V780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:38966026 C>G maps to NM_000540.2 L1410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:38948879 G>A maps to NM_000540.2 G705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr19:38949945 C>T maps to NM_000540.2 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr19:39025832 C>T maps to NM_000540.2 L3804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:38934787 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr19:39018300 G>A maps to NM_000540.2 P3567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr1:237789060 G>A maps to NM_001035.2 K2041K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr1:237801746 G>T maps to NM_001035.2 G2295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr1:237949318 T>A maps to NM_001035.2 S4437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FH-01A-11D-A38G-08 chr1:237881782 C>T maps to NM_001035.2 R3506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr1:237729961 G>T maps to NM_001035.2 E1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:237806718 C>T maps to NM_001035.2 I2438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:237819280 C>G maps to NM_001035.2 S2709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:237619913 C>T maps to NM_001035.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:237872848 C>T maps to NM_001035.2 I3404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:237617808 G>T maps to NM_001035.2 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:237732468 G>T maps to NM_001035.2 E1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:237774084 A>G maps to NM_001035.2 G1569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:237787114 A>T maps to NM_001035.2 P1989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:237880545 C>A maps to NM_001035.2 R3458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr1:237872219 T>C maps to NM_001035.2 L3322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr1:237965173 G>A maps to NM_001035.2 V4703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:237947803 G>A maps to NM_001035.2 L4264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr1:237947659 G>A maps to NM_001035.2 A4216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:237947792 C>T maps to NM_001035.2 L4261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:237872192 C>T maps to NM_001035.2 Q3313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr1:237730001 G>A maps to NM_001035.2 W1117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr1:237948026 C>T maps to NM_001035.2 Q4339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:237944908 G>A maps to NM_001035.2 Q3975Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr1:237919634 C>T maps to NM_001035.2 L3731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr1:237993828 G>C did not map to a codon.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:237794756 G>A maps to NM_001035.2 Q2157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr1:237586487 A>G maps to NM_001035.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr1:237791237 C>A maps to NM_001035.2 R2100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr1:237806718 C>T maps to NM_001035.2 I2438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr1:237729876 C>T maps to NM_001035.2 A1075A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr1:237755087 A>T maps to NM_001035.2 R1404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr1:237993843 C>T maps to NM_001035.2 I4890I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:237619913 C>T maps to NM_001035.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr1:237806742 C>T maps to NM_001035.2 A2446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:237969510 C>T maps to NM_001035.2 H4742H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr1:237947251 C>T maps to NM_001035.2 Y4080Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr1:237947780 C>T maps to NM_001035.2 R4257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr1:237875070 C>T maps to NM_001035.2 F3419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr15:34112955 G>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr15:34080599 C>A maps to NM_001036.3 V3257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr15:33938625 T>C maps to NM_001036.3 N1280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr15:34080578 C>A maps to NM_001036.3 L3250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr15:34105681 G>A maps to NM_001036.3 L3468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:33916208 C>T maps to NM_001036.3 P853P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr15:33928728 C>T maps to NM_001036.3 F1178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:33941337 G>T maps to NM_001036.3 V1348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:34130756 C>T maps to NM_001036.3 F4192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr15:33905426 G>A maps to NM_001036.3 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr15:34032093 T>A maps to NM_001036.3 L2573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr15:34064216 G>A maps to NM_001036.3 L2971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr15:33955862 C>T maps to NM_001036.3 L1848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr15:33927950 G>A maps to NM_001036.3 A1104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr15:33928581 G>A maps to NM_001036.3 Q1129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr15:34130807 C>T maps to NM_001036.3 I4209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr15:33955874 G>A maps to NM_001036.3 L1852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr15:33842375 C>T maps to NM_001036.3 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr15:33927950 G>A maps to NM_001036.3 A1104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr15:33954407 C>T maps to NM_001036.3 Y1559Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr15:33990145 C>T maps to NM_001036.3 H2066H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr15:34140553 A>G maps to NM_001036.3 L4520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr1:153604178 G>A maps to ENST00000368698 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr1:153591382 G>A maps to NM_001024210.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr1:153598930 C>T maps to NM_001024210.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr1:153598930 C>A maps to NM_001024210.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr1:153362975 G>A maps to NM_002964.4 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr1:153333124 G>A maps to NM_002965.3 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:16669142 A>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr4:6698762 C>T maps to NM_005980.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:33292239 G>A maps to NM_022753.2 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:33291960 G>C maps to NM_022753.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr1:33295563 G>T did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:33295664 C>T maps to NM_022753.2 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr1:33292200 G>A maps to NM_022753.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:76171198 C>T maps to NM_130772.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr1:101704752 G>A maps to NM_001400.4 W71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:101705412 C>T maps to NM_001400.4 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr1:101705631 C>T maps to NM_001400.4 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:101704980 G>A maps to NM_001400.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:10335095 G>A maps to NM_004230.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr9:91617098 C>T maps to NM_005226.2 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr9:91616567 G>A maps to NM_005226.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr19:3179293 C>T maps to NM_003775.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr19:3179746 C>T maps to NM_003775.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr19:3179455 C>G maps to NM_003775.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr19:10624574 G>A maps to NM_001166215.1 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr19:10624778 G>A maps to NM_001166215.1 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr11:18254080 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr3:45779282 T>C maps to NM_014016.3 N443N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr13:23929790 G>A maps to NM_014363.4 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr13:23930095 G>A maps to NM_014363.4 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr13:23915125 A>G maps to NM_014363.4 S963S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr13:23904866 G>C maps to NM_014363.4 S4383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr13:23909329 G>A maps to NM_014363.4 N2895N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr13:23915752 G>A maps to NM_014363.4 F754F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr13:23912677 C>G maps to NM_014363.4 S1779S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr13:23905210 G>A maps to NM_014363.4 F4268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr13:23906233 C>T maps to NM_014363.4 A3927A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr13:23904688 G>T maps to NM_014363.4 G4442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr13:23907319 T>C maps to NM_014363.4 K3565K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr13:23910517 G>T maps to NM_014363.4 V2499V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr13:23912526 G>A maps to NM_014363.4 L1830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr13:23909986 T>A maps to NM_014363.4 T2676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr13:23908849 G>C maps to NM_014363.4 V3055V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr13:23906503 C>T maps to NM_014363.4 Q3837Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr19:47653553 C>G maps to NM_005500.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr19:47673085 C>T maps to NM_005500.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr19:47646783 G>A maps to NM_005500.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:5626482 C>G maps to ENST00000433404 S86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:5613500 G>T maps to NM_014649.2 S194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr19:5600271 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr19:5622600 C>T maps to NM_014649.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:134987444 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:134987505 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr23:134994488 G>C did not map to a codon.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr23:134987534 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr23:134993400 C>A did not map to a codon.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr23:134990672 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:134988690 C>T did not map to a codon.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr23:134987436 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:134992291 A>G did not map to a codon.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr23:134988693 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr23:134983818 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:51173804 C>A maps to ENST00000251020 T776T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr16:51171061 G>A maps to ENST00000251020 T1312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr16:51173969 C>T maps to ENST00000251020 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr16:51174260 G>A maps to ENST00000251020 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr16:51173339 C>T maps to ENST00000251020 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr14:21990917 G>A maps to NM_005407.1 L982L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr14:21990938 G>A maps to NM_005407.1 Q975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr14:21991959 G>A maps to NM_005407.1 V634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr14:21993732 G>A maps to NM_005407.1 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr14:21991094 G>A maps to NM_005407.1 Q923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr14:22005045 G>A maps to NM_005407.1 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr14:21993303 T>C maps to NM_005407.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr18:76753466 C>T maps to NM_171999.2 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr18:76755317 G>A maps to NM_171999.2 T1109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:76754549 C>A maps to NM_171999.2 V853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr18:76753097 C>T maps to NM_171999.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr18:76753364 C>A maps to NM_171999.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr18:76753652 G>A maps to NM_171999.2 Q554Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr18:76754423 G>A maps to NM_171999.2 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr18:76754240 C>T maps to NM_171999.2 N750N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:50400860 G>C maps to NM_020436.3 G1035G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:50401019 C>T maps to NM_020436.3 V982V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr20:50408478 C>A maps to NM_020436.3 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr20:50408574 C>T maps to NM_020436.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:14199904 T>A maps to ENST00000269724 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:14199285 G>A maps to ENST00000269724 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr1:874758 C>T maps to ENST00000443100 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr6:130505768 C>T did not map to a codon.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr14:55241652 C>T maps to NM_015589.4 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:39868168 G>A maps to NM_018028.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:39868129 G>A maps to NM_018028.2 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr19:39868163 G>T maps to NM_018028.2 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr19:39868399 G>A maps to NM_018028.2 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr19:39866338 C>G maps to NM_018028.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr19:39868163 G>T maps to NM_018028.2 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr3:169644776 A>T maps to NM_182610.2 K243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr3:169654186 C>T maps to NM_182610.2 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:92732368 C>T maps to NM_017654.3 E1014E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:92731861 C>T maps to NM_017654.3 P1183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:92732940 G>A maps to NM_017654.3 R824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:92733445 G>T maps to NM_017654.3 I655I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr7:92732032 G>A maps to NM_017654.3 V1126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr7:92732695 C>T maps to NM_017654.3 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr7:92732509 C>G maps to NM_017654.3 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr7:92732104 A>G maps to NM_017654.3 A1102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:92731015 C>T maps to NM_017654.3 K1465K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr7:92760766 G>C maps to NM_152703.2 L1506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr7:92763629 G>T maps to NM_152703.2 S552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr7:92763519 G>A maps to NM_152703.2 R589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:92762796 C>A maps to NM_152703.2 E830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr20:35521385 G>A maps to NM_015474.3 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr20:35547850 T>C maps to NM_015474.3 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr22:44364694 C>T maps to NM_015380.4 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr22:44385137 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr22:44385045 A>G maps to NM_015380.4 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr21:15882714 G>A maps to ENST00000285670 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:128700003 C>T maps to NM_001145928.1 L1029L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr2:128707491 C>T maps to NM_001145928.1 W942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:73663484 C>G maps to NM_013260.6 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr17:73663473 C>T maps to NM_013260.6 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr19:55741988 T>C maps to ENST00000443936 P940P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr19:55757020 G>A maps to ENST00000443936 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr22:50869672 C>G maps to ENST00000216061 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr22:50852997 G>A maps to ENST00000216061 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr22:50861947 C>T maps to ENST00000216061 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr11:68370850 G>T maps to NM_001164160.1 E781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:68369378 C>T maps to NM_001164160.1 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:68377462 A>C maps to NM_001164160.1 R854R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr11:68343462 C>T maps to NM_001164160.1 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr11:68377431 C>T maps to NM_001164160.1 P843P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr5:133942732 C>G maps to NM_016103.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr9:136555521 G>A maps to NM_007101.3 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:136599157 C>T maps to NM_007101.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr9:136531910 G>A maps to NM_007101.3 F859F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr9:136599223 C>T maps to NM_007101.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:136596519 G>C maps to NM_007101.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:26708655 C>A maps to ENST00000379061 S300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:26712214 C>T maps to ENST00000379061 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr12:56194386 G>C maps to NM_033082.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr12:56188171 C>A did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:56188172 T>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:109779131 C>T maps to ENST00000369923 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:109779918 C>T maps to ENST00000369923 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr19:39412268 C>T maps to NM_017827.3 E144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:39421109 G>A maps to NM_017827.3 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:65734818 C>T maps to NM_005146.4 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr11:65732635 G>C maps to NM_005146.4 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr12:108917235 A>G maps to NM_014706.3 *964R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:148855933 C>G maps to NM_015278.3 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:148865255 C>T maps to NM_015278.3 Q884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr6:148664259 G>T maps to NM_015278.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr6:148864864 C>G maps to NM_015278.3 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:148852777 C>T maps to NM_015278.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:128922524 T>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:128926407 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr1:100598328 C>G maps to NM_194292.1 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr1:100591462 G>C maps to NM_194292.1 S34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr3:18427953 C>T maps to ENST00000332610 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr3:18390763 C>T maps to ENST00000332610 E764E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr3:18462270 C>T maps to ENST00000332610 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr3:18436384 G>A maps to ENST00000332610 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr3:18391144 C>T maps to ENST00000332610 Q637Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr2:200137184 G>A maps to NM_001172509.1 Q651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr2:200136951 G>A maps to NM_001172509.1 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr2:200137139 G>A maps to NM_001172509.1 Q666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr2:200137113 C>T maps to NM_001172509.1 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr23:84363233 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:84363193 T>C did not map to a codon.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr7:66459243 G>A maps to NM_016038.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr7:66453441 T>C maps to NM_016038.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr22:50893123 G>A maps to ENST00000337034 F1630F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr22:50901313 G>A maps to ENST00000337034 V661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr22:50900021 G>A maps to ENST00000337034 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr22:50887022 G>A maps to ENST00000337034 T1710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr11:10051311 C>T maps to NM_030962.3 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr11:10022531 C>A maps to NM_030962.3 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:10014057 C>T maps to NM_030962.3 E400E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr11:10051356 A>G maps to NM_030962.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr11:10022459 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:9853788 G>A maps to NM_030962.3 Q1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:10215530 G>T maps to NM_030962.3 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:9868504 G>A maps to NM_030962.3 Q978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr11:9834084 G>A maps to NM_030962.3 F1383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr11:9871714 C>T maps to NM_030962.3 E887E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr11:10014033 G>A maps to NM_030962.3 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:28331408 G>T maps to NM_001024401.2 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr19:56041209 G>A maps to NM_001101401.2 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:123806091 A>G maps to NM_001167856.1 D771D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr12:123789170 G>C maps to NM_001167856.1 L1242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr12:123800157 C>G maps to NM_001167856.1 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:1111583 G>A maps to NM_014963.2 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:1123978 G>A maps to NM_014963.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr19:1112416 G>A maps to NM_014963.2 R833R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr19:1119620 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:1112401 G>A maps to NM_014963.2 F838F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:1112018 G>A maps to NM_014963.2 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr19:36018913 G>C maps to NM_001166034.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr17:39967425 G>A maps to NM_006455.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:39959676 G>A maps to NM_006455.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr17:39967425 G>A maps to NM_006455.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr19:50154456 G>T maps to NM_021228.2 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr9:127782984 G>C maps to NM_173690.4 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr9:127790672 A>T maps to NM_173690.4 Y160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr9:127781101 G>A maps to NM_173690.4 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr15:75143778 C>T maps to NM_005697.3 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:155226470 C>T maps to NM_005698.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:155226173 G>A maps to NM_005698.2 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr1:155226075 G>A maps to NM_005698.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr15:75305045 C>G maps to ENST00000361900 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr15:75305072 C>T maps to ENST00000361900 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr15:75308955 G>A maps to ENST00000361900 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr20:34541722 C>A maps to NM_033630.1 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr6:28554482 G>C maps to NM_052923.1 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr6:28540950 T>C maps to NM_052923.1 E905E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr6:28543419 C>T maps to NM_052923.1 Q354Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr6:28543860 G>A maps to NM_052923.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:47458630 G>A maps to NM_012235.2 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:47468687 G>C maps to NM_012235.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr3:47484414 T>C maps to NM_012235.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr3:47467631 C>T maps to NM_012235.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr3:47460152 C>T maps to NM_012235.2 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr3:47459100 G>C maps to NM_012235.2 S888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr3:47459954 G>A maps to NM_012235.2 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr3:47467541 G>A maps to NM_012235.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr15:77067264 A>G maps to ENST00000324767 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr15:76994115 G>A maps to ENST00000324767 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:76994203 G>A maps to ENST00000324767 I801I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:76995294 C>A maps to ENST00000324767 E766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:77087651 T>C maps to ENST00000324767 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr15:77092647 T>C maps to ENST00000324767 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr15:77096935 G>A maps to ENST00000324767 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr15:76958033 T>A maps to ENST00000324767 K869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr15:76797228 A>G maps to ENST00000324767 N975N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr8:27509100 C>T maps to NM_016240.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr8:27737164 C>T maps to NM_173833.5 K424K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:27729501 C>T maps to NM_173833.5 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr8:27845063 G>C maps to NM_173833.5 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:125298762 G>A maps to NM_005505.4 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr12:125271986 C>A maps to NM_005505.4 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:125284768 G>T maps to NM_005505.4 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr12:125298843 C>T maps to NM_005505.4 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:1548931 G>A maps to NM_003693.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr17:1538398 G>A maps to NM_003693.2 Q716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr22:20781782 G>C maps to NM_153334.4 S537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr22:20783845 G>A maps to NM_153334.4 C467C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr22:20785502 G>T maps to NM_153334.4 S219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr22:20780167 G>T maps to NM_153334.4 R704R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:246923503 C>G maps to NM_016002.2 S322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:246927627 T>C maps to NM_016002.2 N357N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr10:102116492 G>A maps to NM_005063.4 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr10:102112129 C>T maps to NM_005063.4 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr4:83557960 G>A maps to NM_001037582.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr4:83552480 C>G maps to NM_001037582.2 *331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr4:54231439 G>A maps to NM_152540.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr4:54232000 C>A maps to NM_152540.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr4:54231769 G>A maps to NM_152540.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:224462209 G>A maps to NM_003469.4 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:224462620 C>T maps to NM_003469.4 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr2:224462209 G>T maps to NM_003469.4 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr15:51981538 C>T maps to NM_013243.3 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr15:52011616 C>G maps to NM_013243.3 S434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr15:52011632 C>T maps to NM_013243.3 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr15:32935873 C>T maps to NM_001144757.1 Y27Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr11:61959666 C>T maps to NM_006552.1 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr11:61978050 G>A maps to NM_002407.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr11:61978050 G>C maps to NM_002407.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr3:159614544 G>A maps to NM_001197113.1 E558E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr7:12668811 C>G maps to NM_001112706.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr4:129864261 C>T maps to NM_144643.2 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr4:129867196 C>T maps to NM_144643.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr4:129867280 C>T maps to NM_144643.2 E440E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr2:239002506 G>A maps to NM_016510.4 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:41494359 G>A maps to NM_001031694.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:41493985 G>T maps to NM_001031694.2 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:41512241 G>A maps to NM_001031694.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr23:17763598 C>A did not map to a codon.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr23:17770058 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:17771497 T>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr23:18278350 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr23:18278393 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr23:18323119 T>C did not map to a codon.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr23:18265987 T>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:18343028 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:18343042 G>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:18338454 C>G did not map to a codon.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr23:18283888 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr23:18259469 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:18342045 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:18275146 G>C did not map to a codon.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr6:108066249 G>A maps to NM_198081.3 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr6:108068028 C>T maps to NM_198081.3 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr3:38739748 G>A maps to NM_006514.2 L1654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr3:38768155 C>A maps to NM_006514.2 E1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr3:38743600 C>G did not map to a codon.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr3:38798218 T>C maps to NM_006514.2 E412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr3:38835306 C>T maps to NM_006514.2 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr3:38783970 A>C maps to NM_006514.2 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:38833581 G>A maps to NM_006514.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr3:38783856 C>T maps to NM_006514.2 V677V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr3:38739574 G>A maps to NM_006514.2 I1712I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr3:38765019 C>A maps to NM_006514.2 E1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr3:38888781 G>C maps to ENST00000302328 L1593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr3:38966936 G>A maps to ENST00000302328 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr3:38888553 T>C maps to ENST00000302328 V1669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:38921614 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:38891990 G>A maps to ENST00000302328 V1436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr3:38950676 A>T maps to ENST00000302328 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr3:38908886 G>T maps to ENST00000302328 I1292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr3:38908898 G>A maps to ENST00000302328 F1288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:38921497 G>A maps to ENST00000302328 F1112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:38962666 G>A maps to ENST00000302328 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr3:38988356 G>A maps to ENST00000302328 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr3:38924743 G>A maps to ENST00000302328 L1067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:38936440 G>A maps to ENST00000302328 F806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr3:38921527 G>A maps to ENST00000302328 I1102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:38888928 G>A maps to ENST00000302328 L1544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:166908449 G>C maps to NM_001165963.1 S248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr2:166848074 G>A maps to NM_001165963.1 Q1904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr2:166915198 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr2:166893007 G>A maps to NM_001165963.1 S993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:166850695 C>T maps to NM_001165963.1 W1604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr2:166848777 C>T maps to NM_001165963.1 A1669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr19:35524617 G>A maps to NM_199037.3 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:35524890 C>G maps to NM_199037.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr2:166229817 G>A maps to NM_001040142.1 L1311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr2:166172018 C>T maps to NM_001040142.1 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:166198840 C>G maps to NM_001040142.1 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr2:166188011 C>G maps to NM_001040142.1 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr2:166187984 C>T maps to NM_001040142.1 I765I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:166246147 C>A maps to NM_001040142.1 P1944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr2:166237239 A>T did not map to a codon.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr2:166245310 C>G maps to NM_001040142.1 L1665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:166231401 C>T maps to NM_001040142.1 Q1394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:165947271 C>T maps to NM_006922.3 W1797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:166020149 C>G maps to NM_006922.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:166019213 C>T maps to NM_006922.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr2:165984599 G>C maps to NM_006922.3 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:165953971 G>A maps to NM_006922.3 L1343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:166019258 C>G maps to NM_006922.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr2:166011105 T>G maps to NM_006922.3 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:165994441 C>A maps to NM_006922.3 E780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr2:166019291 A>G maps to NM_006922.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:165948845 C>T maps to NM_006922.3 L1575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr17:62020201 G>A maps to NM_000334.4 V1424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:62036708 G>A maps to NM_000334.4 F645F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:62022935 G>A maps to NM_000334.4 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr17:62022035 C>T maps to NM_000334.4 K1303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr17:62018712 G>A maps to NM_000334.4 F1643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr17:62020267 G>C maps to NM_000334.4 L1402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr17:62038714 G>A maps to NM_000334.4 C561C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:62018967 C>T maps to NM_000334.4 E1558E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr17:62045479 G>A maps to NM_000334.4 Y313Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr17:62025997 G>A maps to NM_000334.4 F1039F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr17:62022369 C>G maps to NM_000334.4 R1257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr17:62028915 G>A maps to NM_000334.4 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr11:118023347 C>T maps to NM_174934.3 W14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:38597191 C>T maps to NM_001099404.1 K1499K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr3:38651273 C>T maps to NM_001099404.1 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr3:38601886 C>T maps to NM_001099404.1 P1332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr3:38649640 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr3:38591868 A>G maps to NM_001099404.1 S1998S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:38597161 G>A maps to NM_001099404.1 P1509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr3:38648164 G>A maps to NM_001099404.1 Q379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr3:38655513 G>A maps to NM_001099404.1 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr3:38622556 G>A maps to NM_001099404.1 G1031G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:167279807 G>A maps to NM_002976.2 F996F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr2:167263147 G>A maps to NM_002976.2 L1331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr2:167263124 G>A maps to NM_002976.2 Y1338Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr12:52200726 C>T maps to NM_014191.2 L1819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:52100303 C>A maps to NM_014191.2 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:52163049 C>T maps to NM_014191.2 G1101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:52115496 C>G maps to NM_014191.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr2:167056102 C>T maps to ENST00000303354 E1683E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:167151172 C>T did not map to a codon.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr2:167108338 T>C maps to ENST00000303354 G1137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr12:6483631 G>A maps to NM_001159576.1 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr12:6484077 C>A maps to NM_001159576.1 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr12:6457895 G>A maps to NM_001159576.1 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr16:23391755 C>T maps to ENST00000307331 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:23388688 G>A maps to ENST00000307331 W507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr16:23364262 C>T maps to ENST00000307331 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:1226988 G>A maps to NM_001130413.2 *705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr1:1222279 C>T maps to NM_001130413.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:1221397 C>T maps to NM_001130413.2 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr16:23197756 C>T maps to NM_001039.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr16:23200793 G>T maps to NM_001039.3 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr17:10600713 C>G maps to NM_004589.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr22:50962177 G>T maps to NM_001169111.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr22:50962741 C>G maps to NM_001169111.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:53513539 T>G maps to NM_002979.4 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:55083550 G>A maps to NM_021626.2 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr17:55078336 C>T maps to NM_021626.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr8:144891870 G>A maps to NM_182706.3 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr8:144895028 G>A maps to NM_182706.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:144897386 G>A maps to NM_182706.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr8:144896052 G>A maps to NM_182706.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr8:144874977 C>T maps to NM_182706.3 K1359K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr8:144895892 G>A maps to NM_182706.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr8:144895692 G>A maps to NM_182706.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr17:45915931 G>A maps to NM_138355.3 C301C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:45915269 G>T maps to NM_138355.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr17:45915650 C>G maps to NM_138355.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:175263090 C>G maps to NM_024583.4 S27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:175269044 T>C did not map to a codon.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr2:175264774 A>G maps to NM_024583.4 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr8:145559801 G>C maps to NM_031309.4 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr2:120204433 C>G maps to NM_002980.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr2:120204400 G>A maps to NM_002980.2 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:120221746 G>A maps to NM_002980.2 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr22:43604207 G>C maps to NM_173050.2 T868T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr22:43625174 G>A maps to NM_173050.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr22:43606970 G>T maps to NM_173050.2 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr11:9080889 C>T maps to ENST00000457346 K350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr11:9043485 G>C maps to ENST00000457346 L957L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr11:9052472 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr11:9055265 C>A maps to ENST00000457346 E694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:35216388 C>T maps to ENST00000394681 F979F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:35211827 G>C maps to ENST00000394681 R736R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr11:65293602 C>G maps to NM_020680.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr11:65293629 C>T maps to NM_020680.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr11:65293752 C>A maps to NM_020680.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr12:100731226 G>A maps to NM_017988.4 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:100704856 G>T maps to NM_017988.4 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:169845136 A>C maps to NM_181093.2 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:169823674 G>A maps to NM_181093.2 I635I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:169831821 G>A maps to NM_181093.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr1:169831938 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:169825054 C>T maps to NM_181093.2 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr1:169833527 G>A maps to NM_181093.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr4:76878476 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:76895234 G>A maps to NM_018115.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:76882203 G>A maps to NM_018115.2 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:76891495 G>A maps to NM_018115.2 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr4:76882400 G>C maps to NM_018115.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:76894487 G>A maps to NM_018115.2 D231D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:20405116 G>T maps to NM_001006946.1 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:20403794 G>A maps to NM_001006946.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr2:20403858 G>A maps to NM_001006946.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr8:97621772 G>A maps to NM_002998.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:31347174 C>T maps to NM_014654.3 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr8:59494244 G>C maps to NM_005625.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr20:1293282 G>A maps to NM_080489.4 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr14:50269420 G>C maps to NM_004713.3 S647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:50295769 A>G did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr14:50292662 G>C maps to NM_004713.3 S500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:139303519 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:243433446 G>A maps to NM_006642.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr1:243480116 G>A maps to NM_006642.3 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:26976057 G>A maps to NM_006923.2 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr22:21997179 G>T maps to NM_022044.2 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr1:1158732 G>A maps to NM_016176.3 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr1:1158657 G>A maps to NM_016176.3 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:1158657 G>A maps to NM_016176.3 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr5:236601 G>A maps to NM_004168.2 E440E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:61205109 C>G maps to NM_017841.2 S17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7N-01A-11D-A391-08 chr1:17349183 C>T maps to NM_003000.2 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:161284212 G>A maps to NM_003001.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr11:111959636 C>T maps to NM_003002.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:111965690 C>G maps to NM_003002.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr11:111965576 G>A maps to NM_003002.2 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr7:4051843 G>T maps to NM_152744.3 G799G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr7:4171954 A>T did not map to a codon.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr7:4050745 G>A did not map to a codon.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr7:4152938 G>A maps to NM_152744.3 V1151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr7:3990654 A>T maps to NM_152744.3 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr7:4014177 G>T did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr7:3861204 G>A maps to NM_152744.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr7:4153044 G>T maps to NM_152744.3 E1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr7:4116723 C>T maps to NM_152744.3 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr7:4259774 G>A maps to NM_152744.3 G1858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr7:4285426 C>G maps to NM_152744.3 S2124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr17:71391323 G>A maps to NM_001144952.1 Q1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:71348645 G>A maps to NM_001144952.1 F1908F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr17:71334785 G>A maps to NM_001144952.1 P2153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr17:71426747 C>T maps to NM_001144952.1 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr17:71391399 G>A maps to NM_001144952.1 I1162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:71391339 C>G maps to NM_001144952.1 G1182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr17:71410827 G>A maps to NM_001144952.1 N813N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr17:71364668 C>A maps to NM_001144952.1 E1682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:192701029 C>T maps to NM_004657.5 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr2:192711333 G>C maps to NM_004657.5 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:57228774 G>A maps to NM_138969.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr16:82032763 A>G maps to NM_145168.2 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr12:113830898 A>G maps to NM_006843.2 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr12:113835049 G>A maps to NM_006843.2 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr12:113873340 C>G maps to NM_138432.2 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr12:113873355 C>T maps to NM_138432.2 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr17:26691930 G>A maps to NM_001080837.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr18:56816746 C>T maps to NM_033280.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr3:10354377 G>A maps to ENST00000343726 H113H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr3:10353717 C>T maps to ENST00000343726 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr17:75208186 G>A maps to NM_001039573.2 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr22:30812055 C>T maps to NM_012429.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr22:30806615 C>G maps to NM_012429.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr22:30803540 G>A maps to NM_012429.2 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr22:30858093 C>T maps to NM_174975.4 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr22:30887909 C>A maps to NM_174977.3 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr16:5058526 C>T maps to NM_014692.1 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:139371367 C>A maps to NM_014866.1 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr9:139369742 C>T maps to NM_014866.1 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:139370680 C>A maps to NM_014866.1 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr9:139369693 C>A maps to NM_014866.1 E792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr9:139371832 G>A maps to NM_014866.1 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:139369009 G>A maps to NM_014866.1 Q1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:177936897 T>C maps to NM_033127.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:122943995 T>C maps to NM_012430.4 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:145109580 G>A maps to NM_004892.4 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr1:145103955 C>T maps to NM_004892.4 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr1:145112383 C>T maps to NM_004892.4 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr14:39565301 G>A maps to NM_006364.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr14:39555048 G>A maps to NM_006364.2 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr20:18523686 C>T maps to NM_001172745.1 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr20:18513306 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr20:18507015 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr10:121663629 G>A maps to NM_007190.2 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr10:121668557 A>G maps to NM_007190.2 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr5:134002675 C>T maps to NM_021982.1 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr5:134011727 G>T maps to NM_021982.1 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:134041066 C>T maps to NM_021982.1 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr5:134023940 C>T maps to NM_021982.1 Q559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr5:134029514 G>A maps to NM_021982.1 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:134060782 G>A maps to NM_021982.1 *1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr5:134007547 C>T maps to NM_021982.1 Y263Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr5:134015329 C>T maps to NM_021982.1 C431C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr5:134033703 G>A maps to NM_021982.1 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr4:110442740 C>T maps to NM_006323.2 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:110460767 G>C maps to NM_006323.2 R1248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr4:110384479 C>G maps to NM_006323.2 S186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr10:75528783 C>T maps to NM_198597.1 F766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:75523668 T>A maps to NM_198597.1 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr10:75527624 C>T maps to NM_198597.1 Q681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr10:75527762 C>T maps to NM_198597.1 Q727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:75528641 G>A maps to NM_198597.1 V752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr10:75525206 A>C did not map to a codon.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr4:119736284 G>A maps to ENST00000379735 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:119673189 G>C maps to ENST00000379735 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:119678895 G>T maps to ENST00000379735 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr4:119660366 G>A maps to ENST00000379735 Q773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr4:83776176 G>A maps to ENST00000505472 I629I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr4:83740265 G>C maps to ENST00000505472 L1239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:83788010 G>A maps to ENST00000505472 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr4:83776080 C>T maps to ENST00000505472 K661K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr10:102257037 C>T did not map to a codon.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr10:102248676 G>A maps to NM_015490.3 Q1076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr3:127786857 G>A maps to ENST00000464451 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr3:127771729 G>A maps to ENST00000464451 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr3:127779430 C>G maps to ENST00000464451 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr10:12199014 C>T maps to NM_018144.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr10:12199023 C>T maps to NM_018144.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr10:12204225 G>T maps to NM_018144.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr10:12197893 A>T maps to NM_018144.3 K194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr3:169706097 C>T maps to NM_003262.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr3:169710400 C>A maps to NM_003262.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:169694763 C>G maps to NM_003262.3 S59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr6:108193030 C>T maps to NM_007214.4 K720K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:108214764 A>T maps to NM_007214.4 L532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr6:108279135 G>A maps to NM_007214.4 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr6:108227778 G>T maps to NM_007214.4 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr6:108204217 C>A maps to NM_007214.4 E603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:91963046 G>A maps to NM_024077.3 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr15:49288681 C>T maps to NM_001193489.1 K835K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr18:12948140 C>T maps to NM_001013437.1 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr18:12982592 C>T maps to NM_001013437.1 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr18:12982558 C>T maps to NM_001013437.1 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr14:81952723 G>A maps to NM_005065.4 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr20:13856713 G>C maps to NM_025229.1 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr20:13850236 C>T did not map to a codon.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr4:25806346 G>T maps to NM_015187.3 S531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr4:25819814 C>A maps to NM_015187.3 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:169695894 G>C maps to NM_000450.2 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:169696571 A>C maps to NM_000450.2 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:151338295 C>T maps to ENST00000435071 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:151339219 G>A maps to ENST00000435071 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr3:53922427 C>A maps to NM_021237.3 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:169677939 G>A maps to NM_000655.4 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr22:50647057 C>G maps to NM_031454.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr22:50654296 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr22:50655761 C>T maps to NM_031454.1 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr1:169578781 A>G maps to NM_003005.3 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr1:169565211 G>T maps to NM_003005.3 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr1:169565229 G>A maps to NM_003005.3 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr1:169565265 G>A maps to NM_003005.3 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:109017168 G>A maps to ENST00000228463 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr15:101813018 C>T maps to NM_018445.4 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:150321169 C>G maps to NM_016275.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:40009745 G>A maps to NM_182704.1 Q333Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr7:83636799 C>A maps to NM_006080.2 G337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr7:83823833 C>T maps to NM_006080.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr7:83636752 G>A maps to NM_006080.2 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr7:83606466 G>A maps to NM_006080.2 H566H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr7:83592634 C>T maps to NM_006080.2 E582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:80545993 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr7:80380630 C>G maps to NM_006379.2 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr7:80394559 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr7:80546076 G>A maps to NM_006379.2 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr7:84649546 A>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:84702366 G>A maps to NM_152754.2 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr7:84671544 G>C maps to NM_152754.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr7:84642107 G>A maps to NM_152754.2 D586D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr7:84628905 G>A maps to NM_152754.2 D728D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr7:84671601 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr7:84751132 T>C maps to NM_152754.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr7:84651767 C>T maps to NM_152754.2 Q451Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr7:84671601 C>G did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:84694868 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr7:83095818 G>A maps to NM_012431.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:82997264 C>T maps to NM_012431.2 Q655Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr3:50223321 C>T maps to NM_004186.3 Q530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr3:50220146 C>T maps to NM_004186.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr3:50197150 C>T maps to NM_004186.3 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:52473770 G>C maps to NM_020163.1 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr3:52475405 G>A maps to NM_020163.1 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr3:52472133 C>A maps to NM_020163.1 E531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:156146337 G>A maps to NM_022367.3 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:156146607 C>T maps to NM_022367.3 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr1:156131201 C>G maps to NM_022367.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:156146650 C>T maps to NM_022367.3 Q717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:156126263 C>T maps to NM_022367.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr15:90760692 C>T maps to NM_198925.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr15:90764705 C>T maps to NM_198925.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr15:90768318 G>C maps to NM_198925.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr15:90771202 C>G maps to NM_198925.2 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr2:97530100 C>T maps to NM_017789.4 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr2:97533611 G>A maps to NM_017789.4 H4H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:97532105 G>A maps to NM_017789.4 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:97529514 G>C maps to NM_017789.4 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:97530559 G>T maps to NM_017789.4 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:74907020 C>T maps to NM_004263.3 F666F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr10:102732922 G>A maps to NM_017893.2 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr10:102740380 C>T maps to NM_017893.2 H466H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr10:102740933 G>C maps to NM_017893.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:102743314 C>A maps to NM_017893.2 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr10:102740679 C>G maps to NM_017893.2 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr5:9190394 G>T maps to NM_003966.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr5:9197324 C>T maps to NM_003966.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr5:9119186 C>T maps to NM_003966.2 Q616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr5:9224897 C>T maps to NM_003966.2 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr3:122641216 C>T maps to NM_001031702.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:122658316 C>T maps to NM_001031702.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr3:122667458 G>A maps to NM_001031702.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr3:122634452 G>T maps to NM_001031702.2 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr3:122631735 C>T maps to NM_001031702.2 V893V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr3:122647905 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr3:122641123 A>G maps to NM_001031702.2 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr5:115833064 A>T maps to ENST00000257414 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:4550809 C>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:4550943 T>G did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr19:4548447 C>G maps to NM_032108.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr19:4556050 C>A maps to NM_032108.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:4548331 G>C maps to NM_032108.3 S466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr1:151110228 G>A maps to NM_001178061.1 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr1:151110849 C>G maps to NM_001178061.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr1:151107745 G>A maps to NM_001178061.1 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr1:151109451 G>A maps to NM_001178061.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:48062818 C>T maps to NM_153618.1 R687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr15:48052504 A>T maps to NM_153618.1 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr15:48056081 C>T maps to NM_153618.1 N261N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr15:48056885 C>T maps to NM_153618.1 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr15:48063532 C>A maps to NM_153618.1 R925R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr15:48063408 G>A maps to NM_153618.1 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr15:48056216 C>A maps to NM_153618.1 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr15:74707002 G>A maps to NM_003612.3 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr20:43836924 G>A maps to NM_003007.3 Q329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr20:43837173 T>C maps to NM_003007.3 N412N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr20:43836924 G>A maps to NM_003007.3 Q329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr20:43850713 G>A maps to NM_003008.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr20:43850440 T>C maps to NM_003008.2 H56H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr20:43851370 G>A maps to NM_003008.2 Q366Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:48468385 G>A maps to ENST00000004980 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr17:7469081 G>T did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:196612093 C>T maps to NM_152699.4 H14H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:196627283 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:76425251 C>G maps to NM_015571.2 S1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr6:76344527 G>T did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr6:76421111 A>G maps to NM_015571.2 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr3:101136501 A>G maps to NM_020654.3 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr3:101212806 T>C maps to NM_020654.3 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr3:101060618 G>C maps to NM_020654.3 S704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:101086820 G>A maps to NM_020654.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr3:101060533 T>C maps to NM_020654.3 P732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr3:101212741 G>C maps to NM_020654.3 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr3:101049230 C>G did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:87379770 C>G maps to NM_004261.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr1:87379770 C>T maps to NM_004261.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr10:13361207 C>G maps to NM_012247.4 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr16:30456427 C>T maps to ENST00000478753 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr5:42807124 G>A maps to NM_001093726.1 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr4:25160684 G>C maps to NM_016955.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr4:25146649 G>A maps to NM_016955.3 Q304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr4:77952016 G>T maps to ENST00000510515 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr16:4835987 C>T maps to NM_144605.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:55873033 G>A maps to NM_207366.2 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:55863676 T>A maps to NM_207366.2 K410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:55912271 C>T maps to NM_207366.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr2:242277198 G>A maps to ENST00000391972 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr22:42385678 C>T maps to NM_145733.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr17:56598441 C>G maps to NM_004574.3 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr17:56603054 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr17:56598375 C>T maps to NM_004574.3 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr22:19709360 T>C maps to NM_002688.5 H277H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:19709227 G>T maps to NM_002688.5 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr22:19709786 G>A maps to NM_002688.5 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr22:19707404 C>G maps to NM_002688.5 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr23:118786912 A>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr17:75478331 C>T maps to NM_001113491.1 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr17:75484919 C>G maps to NM_001113491.1 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:75484810 G>A maps to NM_001113491.1 W376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr19:48282062 C>G maps to NM_003009.2 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr6:158532516 G>A maps to NM_032861.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr6:158567875 G>C maps to NM_032861.3 S142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr6:158564167 G>A maps to NM_032861.3 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:67890584 G>A maps to NM_001018067.1 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr1:67895854 C>T maps to NM_001018067.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr22:42952595 T>A did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:122775332 A>G maps to NM_020755.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:31906964 C>T maps to NM_178865.4 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:31907021 C>G maps to NM_178865.4 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:43132466 G>A maps to NM_006811.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr20:43150562 G>A maps to NM_006811.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr20:43142654 T>C maps to NM_006811.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr20:43138621 G>A maps to NM_006811.2 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr20:43135593 G>A maps to NM_006811.2 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr20:43139972 G>A maps to NM_006811.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:44087638 G>A maps to ENST00000319327 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr5:79465189 G>C maps to NM_001174072.1 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr5:79441965 G>A maps to NM_001174072.1 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr14:94849286 A>C maps to NM_001127707.1 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr14:94756827 G>A maps to NM_001100607.1 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr14:94756573 C>T maps to NM_001100607.1 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr14:94914895 G>A maps to NM_001080451.1 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr14:94912903 C>T maps to NM_001080451.1 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr14:94953705 C>T maps to NM_173850.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr14:94956022 G>A maps to NM_173850.2 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr14:94962747 C>T maps to NM_173850.2 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr14:94964209 C>T maps to NM_173850.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr14:94964230 C>T maps to NM_173850.2 Q168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr14:94964359 C>T maps to NM_173850.2 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr14:95085751 A>G maps to ENST00000393080 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr14:95033346 C>G maps to NM_006215.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr14:95030139 C>T maps to NM_006215.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:95058572 C>G maps to NM_000624.4 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr14:95057193 G>A maps to NM_000624.4 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:94780793 G>A maps to NM_001756.3 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr14:94780724 G>T maps to NM_001756.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr23:105281022 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:105281030 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:105280481 G>C did not map to a codon.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr23:105280701 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr14:94929549 C>T maps to NM_175739.3 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr14:94929576 A>T maps to NM_175739.3 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr14:94933615 C>T maps to NM_175739.3 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr18:61597342 C>T maps to NM_005024.1 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr18:61377438 C>G maps to NM_080475.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr18:61264389 C>T maps to NM_012397.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr18:61322902 G>A maps to NM_006919.2 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr18:61328327 G>A maps to NM_006919.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr18:61325745 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr18:61306887 C>A maps to NM_002974.2 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:61305117 G>T maps to NM_002974.2 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr18:61308156 T>C maps to NM_002974.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr18:61166360 C>T maps to NM_002639.4 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:2959518 C>T maps to ENST00000316782 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr6:2955832 C>T maps to ENST00000316782 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr18:61471646 C>G maps to NM_001040147.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr18:61471681 C>G maps to NM_001040147.1 S319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr18:61647087 C>T maps to NM_198833.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr18:61654325 T>G maps to NM_198833.1 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr6:2893689 C>G maps to NM_004155.4 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:173881112 G>A maps to NM_000488.3 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr22:21140346 G>T maps to NM_000185.3 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:21133908 G>A maps to NM_000185.3 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr22:21133728 G>A maps to NM_000185.3 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:21138314 G>A maps to NM_000185.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr22:21134136 G>A maps to NM_000185.3 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:100771917 C>T maps to NM_000602.3 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:100771814 G>A maps to NM_000602.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:224849560 C>T maps to NM_001136530.1 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr2:224849560 C>A maps to NM_001136530.1 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr2:224866574 G>A maps to NM_001136530.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr2:224866632 G>A maps to NM_001136530.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr17:1680703 C>G maps to NM_002615.4 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:1673276 G>A maps to NM_002615.4 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr17:1657608 C>T maps to NM_000934.3 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr17:1657611 C>T maps to NM_000934.3 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:57373935 C>T maps to ENST00000403558 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:57381960 C>A maps to ENST00000403558 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr11:57379281 C>T maps to ENST00000403558 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr11:57367473 C>A maps to ENST00000403558 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr11:57382030 C>T maps to ENST00000403558 R537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr11:75280053 C>G maps to NM_001235.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr11:75280083 C>T maps to NM_001235.2 H274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr3:167510379 C>T maps to NM_005025.4 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:167543098 C>T maps to NM_005025.4 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:167543102 G>T maps to NM_005025.4 E409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr3:167512414 T>C maps to NM_005025.4 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr3:167170772 C>T maps to NM_006217.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:40929307 G>T maps to NM_013376.3 S49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr19:40928871 G>C maps to NM_013376.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr2:64863211 G>C maps to NM_014755.2 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr6:109309826 G>A maps to NM_014454.1 I496I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:109415195 G>A maps to NM_014454.1 N27N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr11:94906419 C>T maps to NM_144665.2 *493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:179989196 G>T maps to NM_178123.4 S354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr2:180008497 G>A maps to NM_178123.4 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr2:180008524 C>A maps to NM_178123.4 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr2:180008469 G>T maps to NM_178123.4 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:179981400 A>G maps to NM_178123.4 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:179997074 G>A maps to NM_178123.4 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47W-01A-11D-A23U-08 chr18:42529988 C>T maps to NM_015559.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr18:42531776 T>C maps to NM_015559.2 S824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr18:42531464 C>A maps to NM_015559.2 T720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr18:42532025 C>T maps to NM_015559.2 S907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr18:42531812 C>A maps to NM_015559.2 A836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr16:30972766 C>T maps to NM_014712.1 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr16:30970081 G>A maps to NM_014712.1 Q10Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr16:30995214 G>A maps to NM_014712.1 K1665K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:30977493 C>T maps to NM_014712.1 V764V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr16:30983005 G>A maps to NM_014712.1 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr16:30974835 G>C maps to NM_014712.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr16:30982750 A>T maps to NM_014712.1 S1023S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr16:30977379 C>T maps to NM_014712.1 Y726Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr3:47142963 G>A maps to NM_014159.6 Q1667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:47158212 G>A maps to NM_014159.6 R1496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:47125298 C>A maps to NM_014159.6 E1991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:47142946 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:47142963 G>A maps to NM_014159.6 Q1667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:47163961 G>A maps to NM_014159.6 Q722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr3:47147507 G>A maps to NM_014159.6 F1606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:47147551 G>A maps to NM_014159.6 R1592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:47125626 C>A maps to NM_014159.6 L1881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr14:99932064 C>T maps to NM_032233.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr14:99880244 G>A maps to NM_032233.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr14:99924672 G>C maps to NM_032233.2 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr14:99924698 G>A maps to NM_032233.2 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr3:9483387 C>T maps to ENST00000407969 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr3:9487366 A>G maps to ENST00000407969 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr16:58552845 G>A maps to NM_001160305.1 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr16:58552689 T>C maps to NM_001160305.1 D393D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr4:140441497 G>C maps to NM_030648.2 S232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:123889519 C>G maps to NM_020382.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:123889519 C>T maps to NM_020382.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr12:123875223 G>A maps to NM_020382.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:150915382 G>A maps to NM_001145415.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:150933438 C>T maps to NM_001145415.1 G967G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:150921953 C>T maps to NM_001145415.1 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:150921604 G>A maps to NM_001145415.1 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:150933471 G>A maps to NM_001145415.1 K978K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:150921905 A>C maps to NM_001145415.1 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:150933285 C>T maps to NM_001145415.1 F916F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:150923212 G>A maps to NM_001145415.1 K620K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:150933235 G>T maps to NM_001145415.1 E900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr1:150933492 G>A maps to NM_001145415.1 L985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr1:150900268 C>T maps to NM_001145415.1 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr3:4345156 G>T maps to NM_006515.3 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:135153599 G>A maps to ENST00000372169 F2233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr9:135201795 G>C maps to ENST00000372169 S1730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr9:135224724 G>A maps to ENST00000372169 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr9:135202957 G>A maps to ENST00000372169 L1343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr9:135204825 G>T maps to ENST00000372169 S720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr9:135153500 G>A maps to ENST00000372169 L2266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr9:135153599 G>A maps to ENST00000372169 F2233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr9:135145064 C>T maps to ENST00000372169 L2408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr17:27287863 G>A maps to NM_178860.4 H456H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr17:27308686 C>T maps to NM_178860.4 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr17:27284364 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:26771619 C>A maps to NM_021115.4 S969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:26776230 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr22:26688486 C>A maps to NM_021115.4 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr22:26761375 G>T maps to NM_021115.4 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr22:26692942 C>G maps to NM_021115.4 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:29883604 C>T did not map to a codon.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr16:29888670 G>A maps to NM_201575.2 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr16:29883847 C>G did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr11:64535214 G>A maps to NM_201995.2 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr11:64537843 C>A maps to NM_201995.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr22:30731721 G>C maps to NM_005877.4 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr22:30748977 G>C maps to NM_005877.4 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:30730591 C>T maps to NM_005877.4 R791R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:30733034 C>A maps to NM_005877.4 E696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr22:30733137 G>T maps to NM_005877.4 V661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:2246927 C>T maps to NM_007165.4 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:38453283 G>C maps to NM_006802.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:198257806 T>C maps to NM_012433.2 V1215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr11:65820495 A>G did not map to a codon.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:65831158 C>G maps to NM_006842.2 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr11:65835710 C>T maps to NM_006842.2 T841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:65829179 G>A maps to NM_006842.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr11:65829390 G>A maps to NM_006842.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr16:70575581 C>T maps to NM_012426.4 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr16:70599120 C>T maps to NM_012426.4 Q873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:70605035 G>T maps to NM_012426.4 R1149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:70562803 C>A maps to NM_012426.4 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr6:144416577 G>A maps to NM_031287.2 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:19420948 G>A maps to NM_172231.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr19:19387800 G>A maps to NM_172231.2 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr19:19416814 G>A maps to NM_172231.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:19416844 G>C maps to NM_172231.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr22:31971289 G>A maps to NM_001007467.1 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr22:31942923 G>A maps to NM_001007467.1 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr22:31979904 G>A maps to NM_001007467.1 Q431Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr22:31957368 C>G maps to NM_001007467.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr3:52947575 G>C maps to NM_016329.3 S513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr3:52939152 C>G maps to NM_016329.3 *867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr3:52941648 C>T maps to NM_016329.3 K669K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr3:52962227 G>A maps to NM_016329.3 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr3:52945040 A>C maps to NM_016329.3 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr10:7409680 G>A maps to NM_001018039.1 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr10:7262478 G>A maps to NM_001018039.1 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:7230677 G>A maps to NM_001018039.1 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr10:7218075 G>A maps to NM_001018039.1 D620D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:27189726 G>A maps to NM_006142.3 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:35656102 G>A maps to NM_005066.2 Q471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr1:35656102 G>A maps to NM_005066.2 Q471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:35657034 G>A maps to NM_005066.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:35656389 T>A maps to NM_005066.2 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr8:41122823 G>A maps to NM_003012.4 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:154702902 C>T maps to NM_003013.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr4:154702725 C>T maps to NM_003013.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:37955812 C>T maps to ENST00000223214 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr7:37956082 C>T maps to ENST00000223214 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr10:99527600 G>T maps to NM_003015.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:99527339 G>T maps to NM_003015.3 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr10:99529458 G>A maps to NM_003015.3 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:99529452 G>C maps to NM_003015.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr17:56083832 G>A maps to NM_006924.4 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr1:70687339 C>T maps to NM_004768.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr5:65460642 C>T maps to NM_001077199.1 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr5:65474671 C>G maps to NM_001077199.1 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr6:89808515 G>A maps to ENST00000452027 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr19:19115046 G>A maps to NM_001017392.3 I953I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:19106031 G>A maps to NM_001017392.3 Q1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:19106032 G>A maps to NM_001017392.3 F1016F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr19:19135779 G>T maps to NM_001017392.3 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr19:19136462 G>A maps to NM_001017392.3 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr19:19136196 A>G maps to NM_001017392.3 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:19135977 C>T maps to NM_001017392.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr21:33044005 A>G maps to NM_020706.2 N1050N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr21:33064714 G>A maps to NM_020706.2 Q521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr21:33069063 C>T did not map to a codon.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr21:33073480 G>A maps to NM_020706.2 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:1719908 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:1712414 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr23:1712557 G>T did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr23:1719916 C>A did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr23:1719724 G>T did not map to a codon.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr23:1712975 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:1720173 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr17:74733165 G>T maps to NM_003016.4 S26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr17:74732290 C>T maps to NM_003016.4 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr11:94801095 C>A maps to NM_032102.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:94801071 C>T maps to NM_032102.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr12:46321169 G>A maps to NM_004719.2 Q772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr12:46318786 C>T maps to NM_004719.2 P1210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr12:46320207 C>T maps to NM_004719.2 Q1092Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr12:46322634 A>G maps to NM_004719.2 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:46355559 G>A maps to NM_004719.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:29475689 C>G maps to NM_005626.4 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:29475155 A>G maps to NM_005626.4 H417H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr14:70237197 C>T maps to NM_006925.3 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr14:70235599 C>T maps to NM_006925.3 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:42086759 C>G maps to NM_006275.5 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr20:42089432 G>T maps to NM_006275.5 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr20:42088731 T>C maps to NM_006275.5 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr12:132203997 G>C did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:132241140 A>T maps to NM_004592.2 K558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr12:132262636 C>T maps to NM_004592.2 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:120903590 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:120907259 G>A maps to NM_003769.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr14:36946211 C>T maps to NM_001101341.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr10:81373760 A>T maps to NM_001093770.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr10:81373715 C>T maps to NM_001093770.2 F213F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-ZF-AA4X-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr2:85894866 C>A maps to NM_198843.2 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr2:85893859 C>T maps to NM_198843.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr2:85892788 G>A maps to NM_198843.2 D186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr10:81701776 G>A maps to NM_003019.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr10:104497497 C>G maps to NM_178858.4 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr10:104497515 C>G maps to NM_178858.4 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr10:104491932 C>T maps to NM_178858.4 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr10:104492631 C>T maps to NM_178858.4 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr10:104489105 A>G maps to NM_178858.4 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr10:102799278 G>C maps to NM_030971.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr10:120925083 C>A maps to NM_213649.1 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr2:73285716 G>A maps to NM_144579.2 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr5:156184675 C>A maps to NM_000337.5 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:94232715 T>G maps to NM_001099401.1 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr7:94218030 G>A maps to NM_001099401.1 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr13:23824815 G>A maps to NM_000231.2 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr8:13959953 C>T maps to NM_139167.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr8:14412240 C>T maps to NM_139167.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:153840779 G>A maps to NM_015595.3 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr3:153847390 G>A maps to NM_015595.3 K384K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:153840105 C>T maps to NM_015595.3 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr3:153943703 T>C maps to NM_015595.3 Y665Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr3:153840608 C>G maps to NM_015595.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr1:67147597 C>T maps to ENST00000237247 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:67109285 A>T maps to ENST00000237247 K119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:67147900 C>T maps to ENST00000237247 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:67148014 C>T maps to ENST00000237247 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr1:67101696 C>A maps to NM_032291.2 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr6:134496760 G>A maps to NM_001143678.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr6:134493807 G>A maps to NM_001143676.1 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr6:134498840 G>T maps to NM_001143677.1 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr6:134495196 C>T maps to NM_001143676.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr6:134495695 C>T maps to NM_001143676.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr8:42958921 G>A maps to NM_032237.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr8:42977773 C>T maps to NM_032237.3 H269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr8:42977440 T>C maps to NM_032237.3 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr20:42196349 G>A maps to NM_016276.3 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr20:42213643 C>A maps to NM_016276.3 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr8:8185423 G>C maps to NM_001080826.1 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr8:8185488 G>A maps to NM_001080826.1 Q935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr8:8175695 T>A maps to NM_001080826.1 K1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr8:8175696 C>T maps to NM_001080826.1 L1396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr8:8185378 G>A maps to NM_001080826.1 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:8175696 C>T maps to NM_001080826.1 L1396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr8:8235549 C>T maps to NM_001080826.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr8:8234358 C>A maps to NM_001080826.1 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr8:8176116 G>A maps to NM_001080826.1 L1256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr15:77472429 C>T maps to NM_024776.2 E613E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr15:77471193 T>C maps to NM_024776.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:67771770 C>T maps to NM_013257.3 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr8:67755751 G>A maps to NM_013257.3 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr17:26940125 C>T maps to NM_001174103.1 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr17:26940460 C>T maps to NM_001174103.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:26940676 G>A maps to NM_001174103.1 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr10:52086967 C>T maps to ENST00000361543 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr4:108824403 C>T maps to NM_152621.5 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:108820809 C>T maps to NM_152621.5 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr3:20225183 C>T maps to NM_001012410.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr2:201440105 C>G maps to NM_152524.5 S1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:201437031 G>T maps to NM_152524.5 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:72636306 C>T maps to NM_003901.3 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr10:72633170 C>T maps to NM_003901.3 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr10:72636364 C>T maps to NM_003901.3 R505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr14:64153044 C>A maps to NM_030791.2 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr14:64152823 C>G maps to NM_030791.2 *442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:223389718 C>T maps to NM_152386.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr2:223423424 C>G maps to NM_152386.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr17:78188481 G>C maps to NM_000199.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr22:25308622 C>T maps to NM_001039948.2 F999F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr22:25291228 C>T maps to NM_001039948.2 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr22:25313650 G>A maps to NM_001039948.2 L1040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:2265471 C>T maps to NM_014853.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr17:2265519 G>A maps to NM_014853.2 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr17:2278934 A>T maps to NM_014853.2 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr17:2265478 C>T maps to NM_014853.2 Q125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:40805699 G>A maps to NM_015705.4 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr22:40804818 C>T maps to NM_015705.4 V625V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr22:40801807 C>G maps to NM_015705.4 Y258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:64967756 G>C maps to NM_019072.2 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr16:28878107 G>A maps to NM_001145795.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:28883707 C>T maps to NM_001145795.1 Q571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:28883958 T>A maps to NM_001145795.1 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr16:28883101 G>A maps to NM_001145795.1 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr16:28884771 G>A maps to NM_001145795.1 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr7:101944427 G>C maps to ENST00000306803 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:123504040 C>T did not map to a codon.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr23:123504036 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:162367105 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:156779024 C>T maps to NM_001161441.1 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr19:6760800 C>T maps to NM_005490.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr19:6760836 G>A maps to NM_005490.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr9:130501075 G>A maps to NM_170600.2 L844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:130506923 G>A maps to NM_170600.2 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr8:19190595 G>C maps to NM_022071.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr10:82369197 G>C maps to NM_207372.2 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr1:21050657 G>T maps to ENST00000444387 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:78393320 C>T maps to NM_001101404.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:78386495 C>T maps to NM_001101404.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr15:78393263 C>T maps to NM_001101404.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr15:78393881 G>A maps to NM_001101404.1 E429E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr23:80532490 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr22:38038559 C>T maps to NM_018957.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr22:38040914 G>C maps to NM_018957.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr4:2831313 C>T maps to NM_001145856.1 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr4:2831535 C>T maps to NM_001145856.1 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr4:2828983 C>T maps to NM_001145856.1 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr4:2829041 G>T maps to NM_001145856.1 E229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr2:235943645 G>A did not map to a codon.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr2:235962411 G>A maps to NM_014521.2 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr2:235943714 G>C maps to NM_014521.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr2:235949592 G>A maps to NM_014521.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:15303688 G>A maps to NM_004844.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:15297658 G>A maps to NM_004844.3 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr3:15297739 G>A maps to NM_004844.3 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr3:15303697 C>T maps to NM_004844.3 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr3:15301294 G>A maps to NM_004844.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr4:152086848 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:152096429 G>C maps to NM_001009555.3 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr4:152095861 C>T maps to NM_001009555.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr19:4363776 C>T maps to NM_003025.2 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:4364105 C>T maps to NM_003025.2 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:4361710 G>A maps to NM_003025.2 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr19:4361641 G>A maps to NM_003025.2 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr19:4365532 G>A maps to NM_003025.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr9:17786442 A>G maps to NM_003026.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr9:17791317 C>G maps to NM_003026.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr9:17786484 C>G maps to NM_003026.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:87208004 C>A maps to ENST00000482504 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:131770968 G>A maps to ENST00000372554 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr9:131772473 G>A maps to ENST00000372554 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:131783433 G>A maps to ENST00000372554 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr23:19702050 G>T did not map to a codon.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr23:19854266 A>C did not map to a codon.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr23:19606874 A>G did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:19560285 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:19713820 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr23:19764437 C>G did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:19701994 G>C did not map to a codon.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr23:19587226 C>T did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:19764520 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:19554541 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:19560281 G>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr10:105495507 G>T maps to ENST00000369774 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr10:105361656 A>G maps to ENST00000369774 N1106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr10:105362459 C>A maps to ENST00000369774 E839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr10:105361887 C>T maps to ENST00000369774 K1029K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:171789754 G>A maps to NM_001017995.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr5:171773244 C>T maps to NM_001017995.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr5:171773244 C>T maps to NM_001017995.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr5:171765984 G>A maps to NM_001017995.2 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr5:171765849 C>T maps to NM_001017995.2 Q753Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr5:171774336 C>A did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr4:170038902 G>A maps to NM_020870.3 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr4:170017809 G>A maps to NM_020870.3 Q843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr4:170037710 G>A maps to NM_020870.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr4:170038800 C>T maps to NM_020870.3 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:145393551 C>T maps to NM_152550.3 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:145442002 G>T maps to NM_152550.3 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:145439780 C>T maps to NM_152550.3 I636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr5:145439427 G>C did not map to a codon.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr5:145383694 C>T maps to NM_152550.3 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr4:8220000 G>A maps to NM_018986.3 W281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:8237167 G>A maps to NM_018986.3 Q1097Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:8230147 C>T maps to NM_018986.3 F909F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr4:8242633 G>A maps to NM_018986.3 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr4:8229088 C>T maps to NM_018986.3 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr4:8214431 G>C maps to NM_018986.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr4:8218864 C>G maps to NM_018986.3 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr5:148388495 C>G maps to NM_024577.3 L1132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr5:148386533 G>A maps to NM_024577.3 L1195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr5:148407941 T>C maps to NM_024577.3 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr2:234212 G>C maps to NM_015677.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:218993 C>T maps to NM_015677.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr19:51215332 G>A maps to ENST00000391814 D277D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr19:51217159 C>A maps to ENST00000391814 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr19:51217099 G>A maps to ENST00000391814 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr19:51165527 C>A maps to ENST00000391814 G2068G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr19:51171700 G>A maps to ENST00000391814 S1180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:51171679 C>T maps to ENST00000391814 A1187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr19:51192472 G>A maps to ENST00000391814 F676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr19:51171694 G>T maps to ENST00000391814 G1182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr11:70507824 C>T maps to NM_133266.3 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr11:70332668 G>A maps to ENST00000338508 L1237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr11:70331707 G>A maps to ENST00000338508 Q1558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr11:70332668 G>C maps to ENST00000338508 L1237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:70349009 G>A maps to ENST00000338508 V697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr11:70507699 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr22:51160556 G>A maps to NM_001080420.1 P1448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr22:51143465 C>T maps to NM_001080420.1 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr22:51142339 C>G maps to NM_001080420.1 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr8:145154090 G>A maps to NM_030974.3 Q314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr8:145153855 T>C maps to NM_030974.3 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr9:37948663 C>T maps to NM_003028.2 Q438Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:7533732 G>C did not map to a codon.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr17:7534651 C>G maps to NM_001040.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:7536091 C>A maps to NM_001040.3 S292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr1:154942883 G>T maps to NM_001130040.1 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr1:154942857 G>A maps to NM_001130040.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:154940181 G>C maps to NM_001130040.1 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr1:154936332 G>A maps to NM_001130040.1 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr9:91692808 G>A maps to NM_016848.5 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr9:91667004 G>C maps to NM_016848.5 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr15:49148319 C>A maps to NM_203349.3 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr15:49255181 C>A maps to NM_203349.3 G11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr15:49148227 A>C maps to NM_203349.3 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr16:46650006 G>A maps to NM_024745.4 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:46649951 G>A maps to NM_024745.4 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr16:46638000 G>T maps to NM_024745.4 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr16:46642218 G>T maps to NM_024745.4 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr16:46655240 G>A maps to NM_024745.4 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr19:4284881 C>T maps to NM_020209.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr1:154474265 G>A maps to NM_001010846.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr1:154471627 G>A maps to NM_001010846.2 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:154471659 G>A maps to NM_001010846.2 Q216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr15:45470420 C>T maps to ENST00000437903 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr4:42403227 C>T maps to NM_001080505.1 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr4:42403248 G>C maps to NM_001080505.1 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr3:48510921 G>A maps to NM_016479.3 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr19:41096302 C>T maps to NM_138392.3 A581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr19:41097016 C>T maps to NM_138392.3 D676D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr19:41083166 G>A maps to NM_138392.3 W39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:18250848 G>T maps to NM_004169.3 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr17:18238989 C>T did not map to a codon.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr12:57626563 C>T maps to NM_005412.5 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr12:57625340 G>A maps to NM_005412.5 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:57624778 C>G maps to NM_005412.5 S76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr10:112724251 A>T maps to NM_007373.3 K46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr10:112724766 C>T maps to NM_007373.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr23:591696 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:591740 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr23:601574 G>A did not map to a codon.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr23:591821 G>C did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:595434 C>A did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:595435 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr3:157816075 G>A maps to NM_003030.4 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr3:157815974 T>G maps to NM_003030.4 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:3539489 G>T maps to NM_013276.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr17:3514246 G>A maps to NM_013276.2 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr6:146269462 G>A maps to ENST00000367503 R336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr6:146207827 C>T maps to ENST00000367503 *1688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr6:146216071 C>G maps to ENST00000367503 L1523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr6:146268655 G>A maps to ENST00000367503 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:146243905 C>T maps to ENST00000367503 Q1208Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:72897467 G>A maps to NM_018130.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr5:132160029 G>C maps to NM_001172700.1 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:132159852 G>A maps to NM_001172700.1 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr23:9900214 A>G did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr23:9900618 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr23:9905312 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr23:9914830 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr23:9864258 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr23:9863320 C>T did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr23:9864155 C>G did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:9912779 G>T did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:9862882 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:9914841 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:77660885 G>A maps to NM_020859.3 Q520Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:77691978 C>T maps to NM_020859.3 S1850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:77660798 C>A maps to NM_020859.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr4:77700110 C>T maps to NM_020859.3 F1924F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:77659988 G>T maps to NM_020859.3 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr4:77652088 G>A did not map to a codon.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr4:77660885 G>A maps to NM_020859.3 Q520Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:77675923 C>T maps to NM_020859.3 R1430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr4:77691981 C>G maps to NM_020859.3 L1851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr4:77700045 C>T maps to NM_020859.3 R1903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:50370664 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:50339779 C>G did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:50377283 G>A did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:50377641 G>A did not map to a codon.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr23:50350405 C>T did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:50377469 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:50339779 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:50350865 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:50377208 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr3:164756907 C>T maps to NM_001041.3 V753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:164724635 G>T maps to NM_001041.3 L1458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:164776953 A>G did not map to a codon.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr3:164777731 C>G maps to NM_001041.3 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr3:164750419 G>A maps to NM_001041.3 Q876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr3:164697152 T>A maps to NM_001041.3 S1827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:164755725 G>A maps to NM_001041.3 I796I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr3:164709193 G>A maps to NM_001041.3 V1685V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr11:124509730 G>A maps to NM_170601.3 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr3:150480225 G>A maps to NM_005067.5 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr3:150460158 G>A maps to NM_005067.5 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr3:113304081 G>A maps to ENST00000393830 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr3:113345004 C>T maps to ENST00000393830 F793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr11:117053476 C>T maps to NM_001040455.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr11:117063362 C>T maps to NM_001040455.1 Y685Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr11:407865 G>C maps to NM_021805.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:408081 G>A maps to NM_021805.2 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr20:3673530 C>T maps to NM_023068.3 T1252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr20:3670735 G>C maps to NM_023068.3 V1589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr20:3678469 G>T maps to NM_023068.3 S699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr19:51918852 C>T maps to NM_033130.4 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:51920199 C>T maps to NM_033130.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:51914353 C>T maps to NM_033130.4 *698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr19:51918272 G>A maps to NM_033130.4 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr19:51920677 C>A maps to NM_033130.4 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr19:51920085 C>T maps to NM_033130.4 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr19:50462059 C>G maps to NM_052884.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr19:50455651 C>T did not map to a codon.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr19:50463851 C>A maps to NM_052884.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr19:50461938 G>A maps to NM_052884.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr19:52000607 G>A maps to NM_053003.2 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr19:51995062 C>T maps to NM_053003.2 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr19:52001428 C>T maps to NM_053003.2 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr19:52031054 G>A maps to NM_001245.5 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:52034476 G>T maps to NM_001245.5 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr19:51961613 G>A maps to NM_014442.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr19:51958720 C>T maps to NM_014442.2 Q334Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr19:51960850 C>T maps to NM_014442.2 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:51958762 C>T maps to NM_014442.2 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:51631688 G>A maps to NM_014441.2 K375K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr19:51630504 C>T maps to NM_014441.2 Q323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr19:51628542 G>A maps to NM_014441.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr19:51628938 C>T maps to NM_014441.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr9:34635838 G>A maps to NM_005866.2 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr9:34637057 G>A maps to NM_005866.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr21:44845316 C>T maps to NM_173354.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FM-01A-11D-A38G-08 chr11:111591409 G>A maps to NM_015191.1 Q568Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr11:111594444 C>G maps to NM_015191.1 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr11:111558771 A>T maps to NM_015191.1 K122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:116741050 G>A maps to ENST00000445177 Q595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:116741051 C>A maps to ENST00000445177 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr11:116732088 G>A maps to ENST00000445177 Q769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr11:116744289 C>T maps to ENST00000445177 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr11:116730168 G>C maps to ENST00000445177 V852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:115318965 C>T did not map to a codon.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr5:138283030 C>T maps to ENST00000509534 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr5:138386693 G>A maps to ENST00000509534 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr5:138362488 C>G did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:56355230 G>A maps to NM_006928.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:56351374 G>A maps to NM_006928.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:56349423 G>C maps to NM_006928.3 S529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr12:56349287 G>C maps to NM_006928.3 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr6:100868686 G>T maps to ENST00000262901 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:100841696 G>A maps to ENST00000262901 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WY-01A-11D-A22Z-08 chr6:100838497 C>T maps to ENST00000262901 S680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr6:100896128 C>G did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr6:100868707 G>C maps to ENST00000262901 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr6:100897503 G>A maps to ENST00000262901 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr6:100896392 G>A maps to ENST00000262901 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr6:100841480 G>A maps to ENST00000262901 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr21:38081519 C>T maps to NM_005069.3 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr21:38098554 C>T maps to NM_005069.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr21:38072054 G>A maps to NM_005069.3 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr15:75685102 G>C maps to NM_001145357.1 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr15:75722683 C>T maps to NM_001145357.1 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr15:75684778 G>A maps to NM_001145357.1 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:16974594 C>T maps to NM_015260.1 D489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr19:16976280 A>T maps to NM_015260.1 K514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr19:16982109 C>T maps to NM_015260.1 I863I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr19:16965057 C>A maps to NM_015260.1 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr19:16989122 C>G maps to NM_015260.1 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:16980755 G>A maps to NM_015260.1 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr14:39583535 G>A maps to NM_003616.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr14:39583667 G>A maps to NM_003616.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr14:39583560 G>T maps to NM_003616.2 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr14:39597481 A>T did not map to a codon.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr14:39583590 C>T maps to NM_003616.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr11:65417471 C>A maps to NM_153253.29 S933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:65412520 C>T maps to NM_153253.29 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr11:65417136 G>C maps to NM_153253.29 L877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:65413349 C>G maps to NM_153253.29 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr11:65410011 C>T maps to NM_153253.29 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr14:72176164 C>G maps to NM_015556.1 S1352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:72200446 C>T maps to NM_015556.1 P1663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr14:72090946 A>G maps to NM_015556.1 E604E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr14:72138390 G>A maps to NM_015556.1 E937E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr14:72196848 G>A maps to NM_015556.1 S1585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr14:72139071 C>G maps to NM_015556.1 S946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr14:72090775 G>T maps to NM_015556.1 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:232551309 C>T maps to NM_020808.3 L1564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:232649793 G>C maps to NM_020808.3 S431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:232596868 C>T maps to NM_020808.3 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:232650996 G>C maps to NM_020808.3 S30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr1:232626796 C>T maps to NM_020808.3 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr1:232629404 C>T maps to NM_020808.3 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr19:38655270 C>T maps to NM_015073.1 I1311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:38610500 G>A maps to NM_015073.1 R949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr19:38579388 G>A maps to NM_015073.1 E521E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:38673326 G>A maps to NM_015073.1 W1459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr19:38572483 G>A maps to NM_015073.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:38633218 C>T maps to NM_015073.1 V1134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr19:38682829 G>A maps to NM_015073.1 L1492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr19:38579409 G>A maps to NM_015073.1 V528V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr19:38652998 C>T maps to NM_015073.1 N1256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr19:38689050 C>G maps to NM_015073.1 L1621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr20:1918078 G>A maps to ENST00000400068 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr20:1918132 C>G maps to ENST00000400068 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr20:1902158 C>T maps to ENST00000400068 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr20:1551464 G>C maps to NM_006065.3 S357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr20:1552528 G>A maps to NM_006065.3 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr20:1460372 C>T maps to NM_001122962.1 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:1532441 C>A maps to ENST00000381621 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr20:1616219 T>C maps to NM_018556.3 Q258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr20:1616045 C>T maps to NM_018556.3 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:39374366 C>A maps to NM_012237.3 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:13592070 G>A maps to NM_012241.3 Q140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr17:79872316 C>G maps to NM_016538.2 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr14:61115757 G>C maps to NM_005982.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr14:61113093 C>T maps to NM_005982.3 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr14:61115679 C>T maps to NM_005982.3 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr14:61113246 G>C maps to NM_005982.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:45233485 G>A maps to NM_016932.4 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:61180838 G>A maps to NM_017420.4 F544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr19:46269244 C>A maps to NM_175875.4 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:46271355 G>A maps to NM_175875.4 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr19:46271454 G>C maps to NM_175875.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr19:46271454 G>A maps to NM_175875.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr14:60976256 C>T maps to ENST00000381716 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr18:47917613 C>T maps to NM_145060.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr18:47918544 G>A maps to NM_145060.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:57232375 G>C maps to NM_001100595.1 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr13:21732241 G>C maps to NM_145061.5 S313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:46239836 C>G maps to NM_003726.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr17:46262210 T>A did not map to a codon.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:46247986 G>A maps to NM_003726.3 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr7:26765125 A>G maps to NM_003930.3 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr7:26709766 G>A maps to NM_003930.3 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr1:2160558 G>A maps to NM_003036.3 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:2160702 C>T maps to NM_003036.3 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr3:170099113 C>G maps to NM_005414.3 S394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr3:170108170 C>T maps to NM_005414.3 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:170079093 G>A maps to NM_005414.3 W325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:170108877 C>T maps to NM_005414.3 Q576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr6:31929328 G>A maps to NM_006929.4 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr6:31934857 C>T maps to NM_006929.4 V806V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr5:54640369 A>G maps to NM_015360.4 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr5:54624597 A>G maps to NM_015360.4 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:133496721 C>A maps to NM_170679.2 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:133502934 C>T did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr20:35243656 G>C maps to NM_032214.2 S168*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DK-AA6S-01A-21D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:160589631 C>T maps to NM_003037.2 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:160593910 C>T maps to NM_003037.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:159802971 G>A did not map to a codon.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr1:159923426 G>C maps to NM_033438.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr14:70252942 A>G maps to NM_003049.3 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr13:103701708 G>C maps to NM_000452.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr23:153717248 G>C did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:153716109 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:153716928 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:153716964 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:153715958 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:153715846 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:153717064 G>C did not map to a codon.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr4:48485964 C>T maps to NM_152679.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr4:48486165 C>A maps to NM_152679.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr8:82606748 C>T maps to NM_001010893.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:87770172 G>A maps to NM_197965.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:219259408 C>G maps to NM_000578.3 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr2:219255979 C>T maps to NM_000578.3 N338N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr12:51389480 G>C maps to NM_001174125.1 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr15:48551507 G>T maps to NM_000338.2 V718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr15:48548006 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr5:127485725 C>T maps to NM_001046.2 F681F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr5:127484462 C>T maps to NM_001046.2 N633N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:127420158 C>T maps to NM_001046.2 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr5:127483418 C>T maps to NM_001046.2 Q627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr5:127487014 T>C maps to NM_001046.2 I730I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr5:127485734 A>G maps to NM_001046.2 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:56899425 C>G maps to NM_000339.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr16:56920341 C>G maps to NM_000339.2 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr16:56921889 G>A maps to NM_000339.2 K744K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:67980503 C>T maps to NM_005072.4 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr16:67984323 G>A maps to NM_005072.4 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr16:67979897 G>A maps to NM_005072.4 L899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr16:67986271 C>A maps to NM_005072.4 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr16:67980926 G>C maps to NM_005072.4 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr16:67981313 C>T maps to NM_005072.4 G664G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr16:67995561 G>C maps to NM_005072.4 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr20:44676661 C>T maps to NM_001134771.1 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr20:44672549 G>T maps to NM_001134771.1 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:44665387 C>G maps to NM_001134771.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:44670171 C>T maps to NM_001134771.1 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr20:44665957 C>T maps to NM_001134771.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr20:44680354 C>T maps to NM_001134771.1 F764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr15:34628776 G>A maps to NM_133647.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:34537956 G>A maps to NM_133647.1 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:34537961 G>A maps to NM_133647.1 Q586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr15:34628824 C>T maps to NM_133647.1 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr5:1074712 C>A maps to NM_006598.2 E681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:1064230 G>C maps to NM_006598.2 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:1076836 G>A maps to NM_006598.2 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr5:1074782 G>A maps to NM_006598.2 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:1081815 C>T maps to NM_006598.2 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:1081818 C>T maps to NM_006598.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr5:1074713 C>T maps to NM_006598.2 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:1087071 C>T maps to NM_006598.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:124829152 A>C maps to NM_001195483.1 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr3:124837678 G>A maps to NM_001195483.1 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr7:100456487 C>T maps to NM_020246.2 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr7:100453340 C>A maps to NM_020246.2 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr7:122809277 G>A maps to NM_022444.3 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr7:122768972 G>A maps to NM_022444.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:26820717 C>T maps to NM_001145975.1 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:26817404 T>C maps to NM_001145975.1 H104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:26818798 C>T maps to NM_001145975.1 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:26824193 C>T maps to NM_001145975.1 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr17:26821082 C>T maps to NM_001145975.1 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr17:26816302 C>T maps to NM_001145975.1 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr20:45192107 G>T maps to NM_022829.5 S526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr20:45216780 G>A maps to NM_022829.5 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr20:45221094 G>A maps to NM_022829.5 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:135376054 G>T maps to NM_012450.2 S446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr17:6610376 G>A maps to NM_177550.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:6589553 C>T maps to NM_177550.3 W560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr18:43216987 C>T maps to NM_007163.3 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr18:43212368 G>A maps to NM_007163.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr18:43219850 G>A maps to NM_007163.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr18:43262297 C>A maps to NM_007163.3 P859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr18:43205652 C>G maps to NM_007163.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr18:43221186 C>A maps to NM_007163.3 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr18:43249311 G>A maps to NM_007163.3 W693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr13:99374129 C>G maps to NM_005073.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr13:99371506 G>C maps to NM_005073.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:121642097 G>A maps to NM_021082.3 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr11:60718864 G>A maps to NM_016582.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr12:129293414 C>T maps to ENST00000376744 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:129293994 C>T maps to ENST00000376744 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:113460505 C>T maps to NM_003051.3 W174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:113464732 C>T maps to NM_003051.3 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:113459917 G>C maps to NM_003051.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:113456584 A>C maps to NM_003051.3 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr1:113456599 C>A maps to NM_003051.3 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr1:113456622 C>A maps to NM_003051.3 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:6941693 C>T maps to NM_201566.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:230902145 G>A maps to NM_152527.4 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr2:230911283 G>A maps to NM_152527.4 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr2:230910725 G>A maps to NM_152527.4 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr23:73744290 C>T did not map to a codon.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr23:73751255 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:73744582 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr23:73745727 G>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:73641813 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr23:73749266 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:80196576 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr17:73096807 C>T maps to ENST00000450736 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:73096792 C>T maps to ENST00000450736 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:73096825 C>T maps to ENST00000450736 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr17:73100104 C>T maps to ENST00000450736 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:73089808 C>T maps to ENST00000450736 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:66270074 G>A maps to NM_004694.4 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:66267781 C>T maps to NM_004694.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:66274387 C>T maps to NM_004694.4 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr12:60165123 C>T maps to NM_004731.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:60165016 T>C maps to NM_004731.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:60168666 C>G maps to NM_004731.3 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr12:60168918 G>T maps to NM_004731.3 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr12:60173276 C>T maps to NM_004731.3 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr22:38476985 G>A maps to NM_013356.2 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr10:61413874 G>A maps to NM_194298.2 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr10:61413838 G>A maps to NM_194298.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr6:25811930 G>C maps to NM_005074.3 S322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:25819326 A>C maps to NM_005074.3 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr6:25811917 C>G maps to NM_005074.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr6:25921505 A>T maps to NM_005835.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr6:25915985 C>T maps to NM_005835.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr6:25918737 C>T maps to NM_005835.2 W209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr6:25921499 C>T maps to NM_005835.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr6:25861870 G>C maps to NM_001098486.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr6:25777064 C>G maps to NM_005495.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr6:25777133 C>T maps to NM_005495.2 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:25777133 C>T maps to NM_005495.2 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr6:74354240 C>T maps to NM_012434.4 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr6:74304800 C>T maps to NM_012434.4 *496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr11:22399000 T>C maps to NM_020346.2 Y488Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr11:22399156 C>A maps to NM_020346.2 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr19:49937245 G>C maps to NM_020309.3 S232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr19:49934670 G>C maps to NM_020309.3 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr19:49934655 G>A maps to NM_020309.3 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr12:100751231 G>A maps to NM_139319.2 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr12:100813591 G>C did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr12:100797868 T>C maps to NM_139319.2 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr12:100774577 C>T maps to NM_139319.2 C67C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:61588227 G>A maps to NM_022082.3 W57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr20:61597891 C>T maps to NM_022082.3 N359N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr10:119014866 C>G maps to NM_003054.4 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr10:119013595 T>C maps to NM_003054.4 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr10:119014791 C>A maps to NM_003054.4 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr10:119026536 C>T maps to NM_003054.4 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr10:50819247 G>A maps to NM_003055.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr10:50819478 C>T maps to NM_003055.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr10:50819358 C>T maps to NM_003055.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr10:50819709 C>T maps to NM_003055.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr10:50820029 C>G maps to NM_003055.2 S415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr10:50820267 C>T maps to NM_003055.2 Y494Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr10:50820303 C>T maps to NM_003055.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr21:46951333 G>A maps to NM_194255.1 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr21:46950820 G>A maps to NM_194255.1 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr21:46935619 C>G maps to NM_194255.1 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:169446800 G>A maps to NM_006996.2 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:169437399 G>A maps to NM_006996.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr2:228552262 T>A maps to NM_025243.3 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr9:4574008 G>C maps to NM_004170.5 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr9:4576108 C>T maps to NM_004170.5 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr11:35339006 G>T maps to NM_004171.3 S25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr5:36671302 G>A maps to NM_004172.4 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr2:65243630 C>T maps to NM_003038.4 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr2:65245357 C>G maps to NM_003038.4 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:65248204 C>T maps to NM_003038.4 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:65245288 C>T maps to NM_003038.4 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:65217169 C>T maps to NM_003038.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:65237849 C>T maps to NM_003038.4 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr2:65245210 G>A maps to NM_003038.4 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr2:65243798 C>T maps to NM_003038.4 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr19:47290955 G>A maps to NM_005628.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:47278982 G>A maps to NM_005628.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr19:47280251 G>T maps to NM_005628.2 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr19:47280508 G>A maps to NM_005628.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr19:47280589 G>A maps to NM_005628.2 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr1:53555494 G>C maps to NM_006671.4 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr1:53558460 T>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:113417183 C>G maps to NM_005415.3 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:113414771 T>C maps to NM_005415.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr8:42294607 C>T maps to NM_006749.3 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr8:42302197 G>C maps to NM_006749.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:160555031 C>T maps to NM_003057.2 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BS-01A-21D-A26M-08 chr6:160564642 C>T maps to NM_003057.2 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr11:63066418 G>A maps to NM_001039752.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr11:64335106 C>T maps to NM_018484.2 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr11:64359153 C>A maps to NM_144585.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:64366308 G>C maps to NM_144585.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr11:64366377 T>C maps to NM_144585.2 C351C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr11:64360945 C>T maps to NM_144585.2 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr3:38318946 A>G maps to NM_004256.3 T549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr3:38307470 C>G maps to NM_004256.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr3:38347690 G>C maps to NM_004803.3 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:38359723 C>G maps to NM_004803.3 S590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:38349056 G>A maps to NM_004803.3 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr3:38357067 C>G maps to NM_004803.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:38354934 T>C maps to NM_004803.3 N374N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr3:38350535 C>T maps to NM_004803.3 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:116574151 C>T maps to NM_018420.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:110763561 C>T maps to NM_033125.2 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr14:23818516 G>A maps to NM_020372.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:2929500 C>T maps to NM_002555.5 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr6:160679777 G>A maps to NM_003058.3 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:160664742 G>A maps to NM_003058.3 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr6:160663434 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr6:160671697 G>C maps to NM_003058.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr6:160662557 G>A maps to NM_003058.3 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr6:160638469 C>T maps to NM_003058.3 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:3285314 G>C maps to ENST00000436008 S526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr6:3284171 C>A maps to ENST00000436008 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr11:62911002 C>T maps to NM_001136506.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr6:160829860 A>T maps to ENST00000392145 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr6:160819069 C>G maps to ENST00000392145 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr5:131670479 G>C maps to NM_003059.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr5:131676309 G>A maps to NM_003059.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr11:62748773 C>T maps to NM_004790.3 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:62747215 C>T maps to NM_004790.3 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr11:62747379 G>A maps to NM_004790.3 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr6:43269967 G>C maps to ENST00000372585 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr6:43266371 C>T maps to ENST00000372585 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr6:43267168 G>A maps to ENST00000372585 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:62763270 C>T maps to ENST00000430500 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr11:62763285 G>C maps to ENST00000430500 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr11:63173967 G>C did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr5:138718195 G>A maps to NM_152685.3 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr5:138707767 G>C maps to NM_152685.3 S579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:4848511 G>A maps to NM_203327.1 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr20:4854732 G>A maps to NM_203327.1 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr20:4837815 C>T maps to NM_203327.1 K585K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:220032962 G>C maps to NM_001144890.1 S259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr15:65944007 G>T maps to NM_004727.2 E932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr9:19576937 C>T maps to NM_020344.2 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr9:19786780 A>G maps to NM_020344.2 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr20:19664856 C>T maps to NM_020689.3 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr20:19701738 C>T maps to NM_020689.3 F630F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr20:19662606 C>T maps to NM_020689.3 C291C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr20:19665953 G>T maps to NM_020689.3 E425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:19654268 G>C maps to NM_020689.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr20:19673942 G>A maps to NM_020689.3 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr14:92909096 C>T maps to NM_153646.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr15:48426534 C>T maps to NM_205850.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:113737680 G>A maps to NM_024959.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr12:113742152 C>T maps to NM_024959.2 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:113737617 G>A maps to NM_024959.2 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr12:113744300 G>A maps to NM_024959.2 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr12:113759132 C>G maps to NM_024959.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:113756832 G>C maps to NM_024959.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr22:19163735 G>A maps to NM_005984.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr17:79684041 G>A maps to ENST00000331531 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:4841335 C>T maps to NM_003562.4 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:172669969 C>T maps to NM_003705.3 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr2:172690500 G>A maps to NM_003705.3 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:129483253 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:129499586 G>A did not map to a codon.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr13:41383685 G>A maps to NM_014252.3 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr10:70252892 A>C maps to NM_152707.2 Y202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr22:41188637 G>C maps to NM_006358.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr22:18072956 C>G maps to NM_031481.1 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:73282712 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr17:73269532 C>T maps to NM_021734.4 *321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr5:140683342 G>A maps to NM_031947.2 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr3:48936179 G>C maps to NM_000387.4 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr14:37198765 G>A maps to NM_030631.3 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr11:792031 C>T maps to NM_001191061.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr19:6444306 C>T maps to NM_024103.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:108742613 C>T maps to NM_013386.3 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr1:108697740 G>C maps to NM_013386.3 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr1:108742637 G>T maps to NM_013386.3 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:108686314 C>T maps to NM_013386.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr1:108735219 G>C maps to NM_213651.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr1:108679442 G>A maps to NM_013386.3 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:108679439 T>C maps to NM_013386.3 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:108686332 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:108724615 G>A maps to NM_013386.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr9:130863669 C>G maps to ENST00000373069 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr9:130863463 G>A maps to ENST00000373069 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr6:46630233 C>A maps to NM_004277.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr10:101370695 C>T maps to NM_031212.3 Q335Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr14:100758859 G>A maps to NM_001039355.1 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr14:100758892 G>C maps to NM_001039355.1 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:98989517 A>G maps to NM_213611.2 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr13:45973210 G>C maps to NM_001010875.2 S206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:45973124 G>A maps to NM_001010875.2 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:128651822 C>T maps to NM_031291.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:9613858 C>T maps to NM_032315.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:9633410 C>A maps to NM_032315.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:9613836 G>A maps to NM_032315.2 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:16064425 C>T maps to NM_207348.1 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr17:8197981 A>G maps to NM_201520.1 H48H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:140675470 G>A maps to NM_001104647.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr8:23429028 C>T maps to NM_016612.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr3:39435937 C>T maps to NM_017875.2 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:42398043 C>T maps to NM_001143780.1 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr17:42398542 G>A maps to NM_001143780.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr17:42397440 G>A maps to NM_001143780.1 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr7:87473128 T>C maps to NM_018843.3 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:6426468 C>T maps to NM_173637.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:6427192 C>T maps to NM_173637.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:19218756 G>A maps to NM_178526.3 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr19:19216401 C>T maps to NM_178526.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr19:19217161 C>T maps to NM_178526.3 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr19:19218735 C>T maps to NM_178526.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:19212609 C>G maps to NM_178526.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr23:118586946 G>C did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:156180071 G>A maps to NM_014655.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:65147002 G>A maps to NM_182556.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr5:110097362 G>T maps to NM_138773.1 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:110097169 A>T maps to NM_138773.1 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:1505570 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr23:1508488 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:1508269 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr23:1506238 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr12:58017660 C>T maps to NM_133489.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr12:58016600 G>T maps to NM_133489.2 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr17:78195376 G>C maps to NM_173626.3 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr17:78225190 G>T maps to NM_173626.3 E574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr17:78221935 C>T maps to NM_173626.3 D434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr7:107423682 G>T maps to NM_000111.2 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:107431573 C>T maps to NM_000111.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr7:107414460 G>C maps to NM_000111.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:107430025 G>C maps to NM_000111.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr7:107423792 G>A maps to NM_000111.2 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr7:107427324 G>T maps to NM_000111.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr7:107408353 C>G did not map to a codon.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr7:107353040 G>T maps to NM_000441.1 E765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr7:107342405 C>G maps to NM_000441.1 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr7:107329645 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:107323723 C>T maps to NM_000441.1 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr7:107315424 G>A maps to NM_000441.1 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr7:107335097 G>T maps to NM_000441.1 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr7:107335134 C>T maps to NM_000441.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr7:103032094 G>A maps to ENST00000354356 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr7:103018060 C>T maps to ENST00000354356 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:48671064 C>T maps to NM_022911.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:48665890 C>T maps to NM_022911.2 Q592Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr3:48668455 C>G maps to NM_022911.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr3:48665938 C>T maps to NM_022911.2 K576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr3:48669189 G>A maps to NM_022911.2 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:48665959 G>A maps to NM_022911.2 V569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr8:92307759 C>T maps to NM_134266.1 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr8:92307792 C>T maps to NM_134266.1 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr8:92355618 A>G maps to NM_134266.1 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr8:92352679 C>T maps to NM_134266.1 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr6:35928811 G>C maps to NM_052961.3 S509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr6:35923091 G>C maps to NM_052961.3 S690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:35945030 G>A maps to NM_052961.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:205892741 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:205897035 C>T maps to NM_134325.2 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr1:205898415 G>A maps to NM_134325.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:17611151 C>A maps to NM_198580.1 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:17611370 C>G maps to NM_198580.1 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr19:17598005 C>T maps to NM_198580.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:50474725 G>A maps to NM_003645.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr15:50518204 G>A maps to NM_003645.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr15:50489835 C>A maps to NM_003645.3 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr1:153750360 G>A maps to ENST00000271857 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr9:131122670 G>A maps to NM_005094.3 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:59010558 C>A maps to NM_012254.2 E566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:59022229 G>A maps to NM_012254.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr19:59010947 C>G maps to NM_012254.2 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr19:59012739 G>C maps to NM_012254.2 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr15:85478265 G>A maps to NM_004213.3 Q408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr15:85431056 G>A maps to NM_004213.3 E22E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr15:85452004 C>G maps to NM_004213.3 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr15:45558280 C>T maps to NM_004212.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:86895725 G>A maps to NM_022127.2 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:86917178 G>A maps to NM_022127.2 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr9:86955490 G>A maps to NM_022127.2 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr9:86900258 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr9:86900855 A>G did not map to a codon.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr6:44197676 G>A maps to ENST00000313248 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr6:44197525 G>A maps to ENST00000313248 Q183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr6:44197441 C>T maps to ENST00000313248 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr11:66130933 G>A maps to NM_001532.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr11:66131859 G>A maps to NM_001532.2 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:73122190 C>T maps to NM_018344.5 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr7:5338674 C>T maps to NM_153247.2 H313H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr7:5338648 G>T maps to NM_153247.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr7:5330818 G>A maps to NM_153247.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr7:5338674 C>T maps to NM_153247.2 H313H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:43394662 G>A maps to NM_006516.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:43393371 G>A maps to NM_006516.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr1:43395365 C>T maps to NM_006516.2 K255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr1:43393371 G>C maps to NM_006516.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:43396853 C>T maps to NM_006516.2 Q46Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:43408917 T>C maps to NM_006516.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr20:45362454 G>A maps to NM_030777.3 E536E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr20:45354634 C>A maps to NM_030777.3 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr20:45354268 C>G maps to NM_030777.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr20:45354214 C>T maps to NM_030777.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr20:45355614 C>T maps to NM_030777.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr20:45355596 C>T maps to NM_030777.3 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr20:45355599 C>A maps to NM_030777.3 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr20:45354004 C>T maps to NM_030777.3 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr20:45355599 C>T maps to NM_030777.3 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr20:45355614 C>T maps to NM_030777.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr22:24226014 G>C maps to NM_030807.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:134350212 G>C maps to NM_145176.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr6:134349992 C>A maps to NM_145176.2 G324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:134349750 G>A maps to NM_145176.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:134350042 G>T maps to NM_145176.2 S307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:40499283 G>A maps to NM_052885.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr12:40499376 G>A maps to NM_052885.3 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr12:40223951 G>A maps to NM_052885.3 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:40499175 G>A maps to NM_052885.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr12:7970477 G>A maps to NM_153449.2 C431C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr12:7970582 G>C maps to NM_153449.2 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr3:170724987 T>A maps to NM_000340.1 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr3:170716011 G>A maps to NM_000340.1 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr3:170723894 C>G did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr12:8083899 G>T maps to NM_006931.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:8085602 G>C maps to NM_006931.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr12:8086444 T>C maps to NM_006931.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr12:8078451 G>A maps to NM_006931.2 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr17:7187948 G>A maps to NM_001042.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:7187648 C>T maps to NM_001042.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr1:9107779 G>A maps to NM_003039.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr1:9098068 G>A maps to NM_003039.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr9:136337169 G>A maps to NM_017585.3 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr9:136337151 G>A maps to NM_017585.3 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr9:136337193 C>G maps to NM_017585.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr9:136337289 G>A maps to NM_017585.3 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr9:136341395 G>A maps to NM_017585.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:9083071 G>A maps to NM_207420.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr9:130167103 C>T maps to NM_014580.3 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr9:130167754 C>T maps to NM_014580.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr4:9987350 G>A maps to NM_020041.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:27480786 G>A maps to NM_003459.4 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr15:45814249 C>T maps to NM_013309.4 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr15:45814237 C>T maps to NM_013309.4 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr15:45814288 C>T maps to NM_013309.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr15:45814198 G>C maps to NM_013309.4 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:68412386 G>A maps to NM_022902.2 E413E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:32418956 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:101362197 G>A maps to NM_133496.4 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:101377759 C>T maps to NM_133496.4 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr8:118159213 G>A maps to NM_173851.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr8:118183349 C>T maps to NM_173851.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr8:118147610 C>G maps to NM_173851.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr8:118159372 C>T maps to NM_173851.2 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr4:42051473 C>G maps to NM_006345.3 S273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr4:42069147 T>C maps to NM_006345.3 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr4:42025318 A>G maps to NM_006345.3 K176K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr9:116022659 C>A maps to NM_001859.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr9:116021043 G>A maps to NM_001859.3 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr20:37356483 C>G maps to NM_080552.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:37357140 C>G maps to NM_080552.2 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr20:37357239 C>G maps to NM_080552.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr20:37357146 C>T maps to NM_080552.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr20:37353466 C>T maps to NM_080552.2 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr20:37357119 G>A maps to NM_080552.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr20:37356606 C>T maps to NM_080552.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr20:37356666 C>T maps to NM_080552.2 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:155571324 G>A maps to NM_004733.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr3:155571495 G>A maps to NM_004733.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr3:155571498 T>C maps to NM_004733.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr5:176823848 C>T maps to NM_003052.4 I430I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr4:25677815 G>A maps to NM_006424.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:25664187 A>G maps to NM_006424.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr4:25677779 C>T maps to NM_006424.2 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:140130618 C>T maps to NM_080877.2 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:140128101 C>T maps to NM_080877.2 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr9:140128720 C>T maps to NM_080877.2 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr9:140129071 C>T maps to NM_080877.2 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr1:100459151 C>G maps to ENST00000370153 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:112299548 C>T maps to NM_017945.2 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr3:112300022 C>T maps to NM_017945.2 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:112282360 G>A maps to NM_017945.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr6:44223147 C>T maps to NM_178148.2 W198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:44224225 G>A maps to NM_178148.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr6:44224446 G>A maps to NM_178148.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr6:44222631 G>A maps to NM_178148.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr6:8422705 G>A maps to NM_001142540.1 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr11:45827606 G>T maps to NM_018389.4 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr20:44979475 G>T maps to NM_173179.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr20:44984458 G>T maps to NM_173179.2 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr20:44983599 G>T maps to NM_173179.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr1:67519606 C>A maps to NM_015139.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:67518489 G>C maps to NM_015139.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr1:67519597 C>G maps to NM_015139.2 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr6:137243661 C>T maps to NM_001008783.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr6:137245050 C>A maps to NM_001008783.1 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr6:137245374 C>T maps to NM_001008783.1 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr19:16666172 G>A maps to NM_024881.4 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr19:16677354 G>A maps to NM_024881.4 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:1669759 C>A maps to NM_182838.2 G196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr12:69140309 C>T maps to NM_018656.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr12:69140439 C>T maps to NM_018656.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr6:118588186 G>A maps to NM_001029858.3 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr6:118588270 C>T maps to NM_001029858.3 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr6:118588195 C>T maps to NM_001029858.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr6:118475709 A>G maps to NM_001029858.3 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr6:118635188 A>G did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr11:107673744 G>C maps to NM_017515.4 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr1:234041362 G>T maps to NM_173508.2 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr1:234452394 C>T maps to NM_173508.2 Y292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr1:234458934 G>C maps to NM_173508.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:234452364 C>T maps to NM_173508.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr1:234455892 G>C maps to NM_173508.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr14:58038710 G>A maps to NM_001080455.1 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:150847395 C>A maps to NM_078483.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr5:150867634 G>A maps to NM_078483.2 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr5:150867634 G>T maps to NM_078483.2 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr5:150701772 C>G maps to NM_181776.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr5:150722534 C>T maps to NM_181776.2 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr5:150712820 G>A maps to NM_181776.2 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr5:150666827 C>T maps to NM_001145017.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr5:150660725 C>T maps to NM_001145017.1 K372K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr5:150668013 A>T maps to NM_001145017.1 L182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr5:150657067 G>A maps to NM_001145017.1 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr11:92916060 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr11:92901202 G>A maps to NM_152313.2 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr21:43982207 G>A maps to NM_018964.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr21:43982267 C>T maps to NM_018964.3 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:124949112 C>T maps to NM_198277.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:124933295 C>T maps to NM_198277.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr7:140043313 C>G maps to NM_207113.1 A408A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-A1AC-01A-11D-A13W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr12:46591571 G>A maps to NM_030674.3 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:79220204 C>T maps to NM_001037984.1 Q837Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:79257210 G>A maps to NM_001037984.1 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:79220393 C>T maps to NM_001037984.1 E774E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:165765170 G>A maps to ENST00000409662 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr2:165802237 C>T did not map to a codon.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr12:46764359 C>G maps to NM_018976.4 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:46761068 C>T maps to NM_018976.4 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr12:46760936 C>A maps to NM_018976.4 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr12:46754959 C>A maps to NM_018976.4 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:46764967 G>A maps to NM_018976.4 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr12:46754988 A>G maps to NM_018976.4 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr3:50255768 C>T maps to NM_006841.4 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:50252976 C>T maps to NM_006841.4 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:50256318 C>T maps to NM_006841.4 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr14:61517299 G>A maps to NM_001172702.1 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr14:61486257 G>C did not map to a codon.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr16:58710201 G>A maps to NM_018231.1 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr16:58705051 G>A maps to NM_018231.1 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:84066982 G>A maps to NM_001080442.1 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr16:84065559 G>A maps to NM_001080442.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:84050815 G>A maps to NM_001080442.1 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:54922435 G>A maps to NM_173514.2 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:54922342 C>G maps to NM_173514.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr1:153932873 C>T maps to NM_014437.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr2:196545681 C>A maps to NM_001127257.1 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr10:18270350 C>T maps to NM_001145195.1 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr10:18250697 C>G maps to NM_001145195.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr10:18280177 T>C maps to NM_001145195.1 H456H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr10:18276474 C>T maps to NM_001145195.1 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:18284583 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr10:18292238 C>A maps to NM_001145195.1 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:18250604 C>T maps to NM_001145195.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:47433960 G>A maps to NM_001128225.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:47436656 C>G maps to NM_001128225.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr14:21469736 G>C maps to NM_014579.3 *310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr14:21469392 C>T maps to NM_014579.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr19:2733468 C>G maps to NM_144564.4 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:56631102 C>T maps to NM_001135195.1 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr18:33689639 C>T maps to NM_012319.3 Q728Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:103189213 G>T maps to NM_001135146.1 S288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:69920000 G>A maps to NM_018375.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:44539828 C>A maps to NM_000341.3 Y479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:62652682 C>T maps to NM_001012661.1 Q417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:62648797 C>G maps to NM_001012661.1 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:190428685 G>A maps to NM_014585.5 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:190428406 C>A maps to NM_014585.5 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr2:190426705 A>T maps to NM_014585.5 Y538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:205767809 G>A maps to NM_173854.4 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:205779452 G>A maps to NM_173854.4 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:105282952 A>T maps to NM_032148.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:105282829 G>A maps to NM_032148.3 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:105238267 T>C maps to NM_032148.3 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr3:125726026 C>T maps to NM_001008485.1 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr17:1478942 G>C maps to ENST00000382147 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:1478942 G>C maps to ENST00000382147 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr11:57185272 G>A maps to ENST00000428603 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:57193531 C>T maps to ENST00000428603 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr11:57185237 G>A maps to ENST00000428603 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr11:57188793 G>A maps to ENST00000428603 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr9:108125181 C>G maps to NM_080546.3 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr9:108097852 C>T maps to NM_080546.3 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:10745898 C>T maps to NM_020428.3 C372C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:10747141 C>T maps to NM_020428.3 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr19:10753965 G>T maps to NM_020428.3 E676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr19:10741807 C>G maps to NM_020428.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr19:10747258 C>T maps to NM_020428.3 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:10746997 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:95294100 A>G maps to NM_001114106.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr6:31838417 C>T maps to NM_025257.2 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr6:31836982 G>A maps to NM_025257.2 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr6:31838640 G>A maps to NM_025257.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr6:31833509 C>T maps to NM_025257.2 Q513Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:31842777 G>A maps to NM_025257.2 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:75688107 G>T maps to NM_152697.4 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr1:75684211 G>A maps to NM_152697.4 R498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr1:8395588 C>T maps to ENST00000377479 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr1:8395588 C>G maps to ENST00000377479 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:8390857 G>A maps to ENST00000377479 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:8399580 C>T maps to ENST00000377479 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:8399746 C>T maps to ENST00000377479 Q691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:8385896 G>T maps to ENST00000377479 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr1:8384397 C>T maps to ENST00000377479 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr1:8390569 G>T maps to ENST00000377479 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr1:8398032 C>T maps to ENST00000377479 F619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:8390432 C>A maps to ENST00000377479 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr5:33964005 G>A maps to NM_016180.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:33963849 G>A maps to NM_016180.3 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr5:33963849 G>A maps to NM_016180.3 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr5:33951758 A>C maps to NM_016180.3 Y352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:205632624 C>T maps to NM_033102.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr1:205632303 G>A maps to NM_033102.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:205628643 G>C maps to NM_033102.2 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr8:142229061 C>T maps to NM_001080431.1 W175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr8:142228319 C>T maps to NM_001080431.1 Q422Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr8:142229827 C>A maps to NM_001080431.1 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr8:142225953 G>A maps to NM_001080431.1 Y564Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:26731742 G>C maps to ENST00000440501 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:26732063 G>A maps to ENST00000440501 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr9:115652088 G>A maps to NM_033051.3 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr9:115649690 G>A maps to NM_033051.3 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr9:115652598 G>A maps to NM_033051.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr9:115652436 G>A maps to NM_033051.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr17:19480736 G>A maps to ENST00000395585 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr17:19451305 G>C maps to ENST00000395585 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr17:19463548 C>T maps to ENST00000395585 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr17:19458571 C>T maps to ENST00000395585 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:19608793 G>C maps to NM_152908.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr17:19582148 G>A maps to NM_152908.3 F553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr17:19619811 G>A maps to NM_152908.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:19582094 C>T maps to NM_152908.3 V571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr17:42336707 G>A maps to NM_000342.3 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr17:42340063 G>A maps to NM_000342.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:162821637 G>A maps to NM_001178015.1 L1038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr2:162762397 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr2:162813746 G>A maps to NM_001178015.1 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr20:3211438 G>T maps to NM_001174090.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr20:3214774 G>C maps to NM_001174090.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr20:3209343 G>A maps to NM_001174090.1 N777N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr2:27887134 G>T maps to NM_018158.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr2:27898483 G>A maps to NM_018158.2 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:27907999 G>T maps to NM_018158.2 E658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:27900719 G>A maps to NM_018158.2 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr7:150772846 C>G maps to NM_003040.3 V1152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:150768672 C>T maps to NM_003040.3 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:150768812 G>A maps to NM_003040.3 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr7:150767331 C>T maps to NM_003040.3 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr7:150772566 G>A maps to NM_003040.3 V1091V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr2:220500048 C>T maps to NM_201574.2 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr2:220504317 C>G maps to NM_201574.2 L1073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr2:220496756 C>T maps to NM_201574.2 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr4:72205109 C>T maps to NM_001098484.2 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr4:72215626 A>G did not map to a codon.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr4:72400083 C>T maps to NM_001098484.2 N807N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr4:72215721 G>A maps to NM_001098484.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr2:74483002 G>A maps to NM_021196.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:74466548 C>T maps to NM_021196.3 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:74489305 C>A maps to NM_021196.3 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr2:74474301 G>A maps to NM_021196.3 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr2:74492306 G>C maps to NM_021196.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:27465553 C>A maps to ENST00000454389 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr3:27446454 C>G did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:27436018 G>C maps to ENST00000454389 S1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:27436146 G>C maps to ENST00000454389 V993V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:27462228 C>A maps to ENST00000454389 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:27463168 C>T maps to ENST00000454389 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:51890799 C>G maps to NM_001039960.1 V991V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr12:51865154 T>C maps to NM_001039960.1 D581D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr12:51845972 G>T maps to NM_001039960.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr12:51868138 C>T maps to NM_001039960.1 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:51851210 C>G maps to NM_001039960.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr5:139748222 C>T maps to ENST00000507527 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr22:32480978 C>T maps to NM_000343.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:32495202 C>T maps to NM_000343.3 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr22:32506038 C>T maps to NM_000343.3 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr22:32487638 C>T maps to NM_000343.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr22:32480978 C>T maps to NM_000343.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr17:18862966 C>T maps to NM_152351.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr16:24920407 C>T maps to NM_052944.2 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr16:24902199 G>A maps to NM_052944.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:24873929 G>A maps to NM_052944.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr16:24902220 G>A maps to NM_052944.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr11:26725109 G>A maps to NM_178498.3 C263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:31499001 C>T maps to ENST00000431354 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr16:31497090 C>T maps to ENST00000431354 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:31500574 C>G maps to ENST00000431354 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr16:31497552 C>T maps to ENST00000431354 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr16:31499001 C>G maps to ENST00000431354 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr21:35468010 C>T maps to NM_006933.4 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr21:35468621 G>C maps to NM_006933.4 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr22:32616909 C>A maps to NM_014227.2 E589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr22:32647855 G>A maps to NM_014227.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr22:32626964 C>G maps to NM_014227.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:32627030 G>A maps to NM_014227.2 C351C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:32627027 C>G maps to NM_014227.2 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr19:17983442 C>T maps to NM_000453.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr19:17988546 G>A maps to NM_000453.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr19:17992961 C>G maps to NM_000453.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr19:17992861 G>C maps to NM_000453.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr19:17988874 C>T maps to NM_000453.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:27430495 G>T maps to NM_021095.2 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr2:108604667 G>A maps to NM_021815.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:108608586 C>T maps to NM_021815.2 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr2:108624954 C>G maps to NM_021815.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:108626704 C>T maps to NM_021815.2 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr2:108626839 T>C maps to NM_021815.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr2:108626902 C>A maps to NM_021815.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr2:108627311 C>T maps to NM_021815.2 Q580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr1:48688515 C>A maps to NM_001135181.1 Y36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:48701485 C>T maps to NM_001135181.1 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr1:48708223 C>T maps to NM_001135181.1 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:48696294 C>G maps to NM_001135181.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr3:11068042 C>G maps to NM_003042.3 S359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr3:11076242 G>A maps to NM_003042.3 Q518Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:11067484 C>T maps to NM_003042.3 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr3:11058950 C>T maps to NM_003042.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:11071035 C>T maps to NM_003042.3 Q441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr3:11058971 C>T maps to NM_003042.3 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:344378 G>A maps to NM_016615.3 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr23:115573894 A>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:115573944 C>A did not map to a codon.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr23:115584267 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr23:115577925 T>G did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:115574826 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:115590058 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr23:115589980 A>G did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr12:85264442 G>A maps to NM_182767.4 Q437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr12:85266413 G>C maps to NM_182767.4 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr19:49797168 G>A maps to NM_014037.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr1:110734727 C>T maps to NM_001010898.2 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:1235674 C>T maps to NM_182632.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr5:1232400 C>T maps to NM_182632.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr5:1239638 C>T maps to NM_182632.2 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:1221313 C>T maps to NM_001003841.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr5:1221322 C>T maps to NM_001003841.2 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:1208933 C>T maps to NM_001003841.2 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr5:1208933 C>T maps to NM_001003841.2 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr5:1217011 C>T maps to NM_001003841.2 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr16:55719099 C>T maps to NM_001043.3 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr16:55736233 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr16:55690821 C>T maps to NM_001043.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr3:45812743 G>A maps to NM_020208.3 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr3:45800487 G>A maps to NM_020208.3 D587D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:45812875 G>A maps to NM_020208.3 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr3:45812854 G>A maps to NM_020208.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr3:45812891 G>C maps to NM_020208.3 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr5:1406323 C>A maps to NM_001044.4 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:1414824 G>A maps to NM_001044.4 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr5:1406365 G>A maps to NM_001044.4 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr5:1406377 G>A maps to NM_001044.4 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr17:28530249 G>A maps to ENST00000394821 F628F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:28530351 G>A maps to ENST00000394821 I594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr11:20623153 G>A maps to NM_004211.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:20668480 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr11:20676317 C>T maps to NM_004211.3 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr11:20673914 C>T maps to NM_004211.3 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr3:14485244 G>T maps to NM_001134367.1 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr3:14508094 G>C maps to NM_001134367.1 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:149576665 C>A maps to NM_014228.3 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr5:149576665 C>T maps to NM_014228.3 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr5:149581907 A>T did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:152958596 C>G did not map to a codon.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr23:152954206 G>C did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr23:152959661 G>T did not map to a codon.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr23:152958603 G>C did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:44474197 C>T maps to NM_201649.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:44463574 G>C maps to NM_201649.2 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr1:44468563 G>C maps to NM_201649.2 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr13:30106970 G>C maps to NM_003045.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr13:30098344 G>A maps to NM_003045.4 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr13:30104736 A>G maps to NM_003045.4 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr13:30110112 C>G maps to NM_003045.4 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr19:33699808 C>T maps to NM_019849.2 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:87241990 G>A maps to NM_138817.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr8:87226752 T>C maps to NM_138817.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr8:87242215 G>A maps to NM_138817.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:170198741 G>A maps to NM_020949.2 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:170201143 C>T maps to NM_020949.2 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr8:17419459 C>T maps to NM_001164771.1 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr8:17422583 C>T maps to NM_001164771.1 Q676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr23:70149566 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr23:70148784 C>T did not map to a codon.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr23:70149566 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:70146412 C>G did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr23:70148355 G>T did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:70147841 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:70145680 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr23:70146020 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr22:21384248 C>A maps to NM_004173.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr22:21384119 C>T maps to NM_004173.2 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr22:21385717 G>A maps to NM_004173.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr22:21384563 G>A maps to NM_004173.2 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr22:21386080 G>A maps to NM_004173.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr22:21384611 G>C maps to NM_004173.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr16:87902737 G>A maps to NM_003486.5 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr16:68324420 G>T maps to NM_003983.4 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr14:23243187 G>A maps to NM_001126106.1 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr14:23282304 C>A maps to NM_001126106.1 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr14:23282232 G>A maps to NM_001126106.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr14:23609765 G>A maps to NM_012244.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr14:23596403 C>T maps to NM_012244.2 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr14:23597255 G>A maps to NM_012244.2 H471H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr14:23598903 C>T maps to NM_012244.2 Q406Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr14:23597297 C>T maps to NM_012244.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr19:33355032 G>A maps to NM_014270.4 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:33334853 G>A maps to NM_014270.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr19:33355209 G>A maps to NM_014270.4 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:40656480 C>A maps to NM_021097.2 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr2:40342584 A>G maps to NM_021097.2 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr2:40655746 C>T maps to NM_021097.2 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:47933516 G>A maps to NM_015063.2 F865F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr19:47944592 C>A did not map to a codon.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr19:47960818 G>A maps to NM_015063.2 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:47951367 C>G maps to NM_015063.2 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr14:70634194 C>T maps to NM_183002.1 E315E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:70633744 G>A maps to NM_183002.1 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr14:70518826 C>G maps to NM_183002.1 V637V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr14:70634425 G>C maps to NM_183002.1 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr14:70512798 C>T maps to NM_183002.1 R883R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr14:70633540 A>T maps to NM_183002.1 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr14:70515700 G>A maps to NM_183002.1 Y730Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr14:70515685 C>T maps to NM_183002.1 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr1:27428506 C>T maps to NM_003047.3 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:27427034 C>T maps to NM_003047.3 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr1:27480686 G>A maps to NM_003047.3 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr3:111962923 C>G did not map to a codon.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr3:111962878 G>A maps to NM_183061.1 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:111950213 T>C maps to NM_183061.1 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:173523899 G>C maps to NM_178527.3 Y423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:103236426 G>A maps to NM_003048.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:103322366 A>G maps to NM_003048.3 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:103300681 C>T maps to NM_003048.3 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr2:103274329 C>T maps to NM_003048.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:103274348 C>T maps to NM_003048.3 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr2:103281671 C>A maps to NM_003048.3 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr5:482239 C>T maps to NM_004174.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:475146 C>T maps to NM_004174.2 S784S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr5:476427 G>A maps to NM_004174.2 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr5:482664 G>A maps to NM_004174.2 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr5:484633 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr5:477487 C>A maps to NM_004174.2 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr5:476391 G>A maps to NM_004174.2 F664F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr5:479977 C>T maps to NM_004174.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr5:483443 G>A maps to NM_004174.2 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:103119998 C>T maps to NM_001011552.3 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:103128723 G>C maps to NM_001011552.3 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:103148874 G>T maps to NM_001011552.3 E709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr2:103095352 C>T maps to NM_001011552.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr2:103130648 C>T maps to NM_001011552.3 Q554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:103142765 C>T maps to NM_001011552.3 Q667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr2:103095541 G>A maps to NM_001011552.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr2:103148828 C>T maps to NM_001011552.3 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr16:67298322 C>T maps to NM_004594.2 F637F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr16:67289056 C>T maps to NM_004594.2 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr16:67286736 T>G maps to NM_004594.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr16:67305025 C>A maps to NM_004594.2 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr23:135126737 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr23:135126622 T>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr23:135095107 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr23:46529103 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:46510552 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:46466592 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr23:46508178 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:48503323 C>T maps to ENST00000417961 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:48466214 C>T maps to ENST00000417961 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr20:48500482 C>T maps to ENST00000417961 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr20:48461610 C>A maps to ENST00000417961 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr20:48500446 G>T maps to ENST00000417961 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr20:48472031 C>T maps to ENST00000417961 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr20:48431706 C>T maps to ENST00000417961 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:143212548 G>A maps to NM_173653.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr3:143100928 C>T maps to NM_173653.3 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr12:21445141 G>A maps to NM_134431.3 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr12:21453441 C>T maps to NM_134431.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr12:21427509 A>C maps to NM_134431.3 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr12:21355521 A>G maps to NM_006446.4 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr12:21353502 G>A maps to NM_006446.4 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr12:21358810 A>G maps to NM_006446.4 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr12:21032478 G>C maps to NM_019844.2 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr12:20854308 C>T maps to NM_017435.4 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr12:20903756 T>C maps to NM_001145946.1 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:20864430 C>A maps to NM_017435.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr12:20885907 A>C maps to NM_017435.4 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr12:20903660 C>T maps to NM_017435.4 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr12:20870078 G>T maps to NM_017435.4 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:20886038 G>C did not map to a codon.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr12:20868202 T>C maps to NM_017435.4 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr12:20870109 C>T maps to NM_017435.4 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr3:133661492 C>G maps to NM_005630.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:74904425 C>T maps to NM_007256.4 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr15:92706130 C>G maps to NM_013272.3 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr15:92706049 G>T maps to NM_013272.3 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr15:92690230 G>A maps to NM_013272.3 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr15:92459365 G>C maps to NM_013272.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:61300306 C>T maps to NM_016354.3 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:61290074 G>A maps to NM_016354.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:61296327 C>G maps to NM_016354.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMW-01A-11D-A42E-08 chr20:61292464 G>A maps to NM_016354.3 K353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr20:61296284 G>A did not map to a codon.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr5:101592817 C>T did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr5:101631644 G>A maps to NM_180991.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:101606433 G>A maps to NM_180991.4 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:70585256 G>A maps to NM_030958.2 F798F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr8:70744788 G>A maps to NM_030958.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:70650367 C>A maps to NM_030958.2 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr8:70744344 G>A maps to NM_030958.2 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr8:70744122 G>T maps to NM_030958.2 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr8:70588852 G>A maps to NM_030958.2 R694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr8:70585511 G>A maps to NM_030958.2 C713C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr8:70744344 G>A maps to NM_030958.2 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr8:70650350 A>C maps to NM_030958.2 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr8:70617324 T>C maps to NM_030958.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr8:70744565 G>A maps to NM_030958.2 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr8:70744737 G>A maps to NM_030958.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:33689907 C>A maps to NM_152270.3 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr17:33689786 C>T maps to NM_152270.3 W347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:33750020 C>T maps to NM_018042.3 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:33749639 G>C maps to NM_018042.3 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:33807128 G>A maps to ENST00000361112 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr17:33849302 G>A maps to ENST00000361112 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:33806508 G>A maps to ENST00000361112 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr17:33807040 G>C maps to ENST00000361112 S92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr17:33768151 G>C maps to NM_144682.5 S719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr17:33768281 C>A maps to NM_144682.5 E676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr17:33769075 G>C maps to NM_144682.5 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr17:33769021 C>T maps to NM_144682.5 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr17:33769075 G>C maps to NM_144682.5 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr17:33772087 T>C maps to NM_144682.5 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr17:33770878 G>T maps to NM_144682.5 S376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:33586668 G>A maps to NM_144975.3 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:33585829 G>T maps to NM_144975.3 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:33592612 C>T maps to NM_144975.3 F794F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:41481831 G>C maps to NM_144990.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:41486185 G>C maps to NM_144990.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr10:98819899 G>A maps to NM_003061.2 N319N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr10:98763894 C>A maps to NM_003061.2 G1265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr10:98762696 G>A maps to NM_003061.2 N1306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr10:98823296 G>A maps to NM_003061.2 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr10:98924592 G>C maps to NM_003061.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:98807754 T>C did not map to a codon.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr10:98819266 G>T maps to NM_003061.2 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr10:98819902 C>T maps to NM_003061.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr10:98778793 G>C maps to NM_003061.2 T939T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr4:20512736 A>G maps to ENST00000273739 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr5:168100245 T>C maps to NM_003062.2 P1259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr5:168189635 G>A maps to NM_003062.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr5:168187934 C>T maps to NM_003062.2 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr13:84454439 G>A maps to NM_052910.1 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:84454043 G>T maps to NM_052910.1 C533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr13:84454943 A>G maps to NM_052910.1 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr13:84453713 C>G maps to NM_052910.1 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr23:144905317 A>T did not map to a codon.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr23:144904562 G>T did not map to a codon.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr23:144904563 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:144904149 C>A did not map to a codon.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr23:144905562 G>C did not map to a codon.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr23:144905669 C>T did not map to a codon.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr23:144905634 T>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:144905809 C>T did not map to a codon.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr23:144906346 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr23:144906441 C>T did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr3:164907373 C>G maps to NM_014926.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr3:164906170 C>T maps to NM_014926.2 K816K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr3:164906998 G>A maps to NM_014926.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:164907883 A>G maps to NM_014926.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr23:142717988 G>T did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:142718375 C>A did not map to a codon.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr23:142717032 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr23:142718201 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:142716759 C>A did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:142716592 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr23:142718329 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:142717277 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr23:142718513 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr23:142718748 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr23:142716794 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:142718437 T>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:142716529 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr23:142718606 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr23:142717329 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:88328434 T>A maps to NM_015567.1 C264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr13:88328194 C>G maps to NM_015567.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr13:88327741 C>T maps to NM_015567.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr13:88329427 C>T maps to NM_015567.1 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr13:88329489 C>G maps to NM_015567.1 S616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr13:88329085 G>A maps to NM_015567.1 Q481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr13:88328194 C>G maps to NM_015567.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr13:88328425 T>C maps to NM_015567.1 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr13:88329001 C>T maps to NM_015567.1 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr13:86370508 T>G maps to NM_032229.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr13:86369794 T>C maps to NM_032229.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr13:86368218 T>G maps to NM_032229.2 R809R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr10:105780290 C>T maps to NM_014720.2 Q1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr10:105777992 G>T maps to NM_014720.2 E985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr3:57827024 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:57827094 C>G maps to ENST00000428312 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr3:57850349 G>T maps to ENST00000428312 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:57908653 G>A maps to ENST00000428312 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr3:57743489 C>T maps to ENST00000428312 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr3:57902668 C>T maps to ENST00000428312 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr3:57898357 G>C maps to ENST00000428312 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:57893609 G>C did not map to a codon.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr20:57611558 C>T maps to NM_016045.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr15:59205828 C>A maps to NM_024755.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr15:59181705 G>A maps to NM_024755.2 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr15:59191804 C>T maps to NM_024755.2 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:59179197 G>A maps to NM_024755.2 I937I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr5:159831860 C>T maps to NM_006425.4 E473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr5:159834988 C>T maps to NM_006425.4 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr5:159835365 C>T maps to NM_006425.4 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr8:143822578 G>C maps to NM_020427.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:146436068 G>T maps to NM_001003688.1 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:146463792 C>T maps to NM_001003688.1 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr18:45368210 G>C maps to NM_001003652.2 S464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr15:67473726 C>T maps to NM_005902.3 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr15:67479781 C>T maps to NM_005902.3 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr15:67477080 C>G maps to NM_005902.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr15:67477080 C>T maps to NM_005902.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr15:67473750 C>G maps to NM_005902.3 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr18:48593466 G>T maps to NM_005359.5 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr15:67073704 C>T maps to NM_005585.4 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr15:67073737 C>T maps to NM_005585.4 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr18:46448212 C>T maps to NM_005904.3 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr18:46447789 G>A maps to NM_005904.3 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr13:37439762 G>C maps to NM_001127217.2 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr13:37453505 C>T maps to NM_001127217.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr12:51639757 G>T maps to NM_001031628.1 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr1:40882741 C>T maps to NM_022733.2 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr23:128657244 G>A did not map to a codon.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:128626022 A>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:128649668 C>A did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:128599885 G>C did not map to a codon.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr23:128638780 T>C did not map to a codon.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr23:128614760 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:128602793 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr23:128622974 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:2060920 C>T maps to NM_003070.3 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:2056766 G>C maps to NM_003070.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B0-01A-11D-A31L-08 chr9:2039778 G>A maps to NM_003070.3 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr9:2110332 G>A maps to NM_003070.3 L1124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:11123725 C>T maps to NM_001128849.1 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:11123776 C>T maps to NM_001128849.1 I809I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr19:11168976 C>T maps to NM_001128849.1 R1523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:11121152 G>A maps to NM_001128849.1 E740E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:11135086 G>C maps to NM_001128849.1 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr19:11144845 C>T maps to NM_001128849.1 A1307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:95201921 G>A maps to NM_001128429.1 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr4:95170810 G>T maps to NM_001128429.1 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T4-01A-11D-A391-08 chr4:95197488 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:217300155 C>T maps to NM_014140.3 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr2:217279831 A>G maps to NM_014140.3 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr2:217279540 G>A maps to NM_014140.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr22:24129391 G>A maps to NM_003073.3 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr22:24175855 G>T maps to NM_003073.3 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr3:47677530 C>T maps to NM_003074.3 V824V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr3:47734737 C>A maps to NM_003074.3 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr12:56578720 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:56575359 G>A maps to NM_003075.3 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr12:56558279 G>A maps to NM_003075.3 F1125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr12:56565556 G>A maps to NM_003075.3 F666F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr12:50483728 G>C maps to NM_003076.4 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr12:50492580 C>T maps to NM_003076.4 R493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr12:50488354 G>A maps to NM_003076.4 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:50480415 G>A maps to NM_003076.4 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr17:61912093 G>A maps to NM_001098426.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:61914374 C>T maps to NM_001098426.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr17:61910949 G>A maps to NM_001098426.1 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr7:150936724 C>T maps to NM_003078.3 Q414Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr7:150939848 C>T maps to NM_003078.3 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr17:38793752 G>C maps to NM_003079.4 Y76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr23:53426597 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr23:53436074 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr23:53432029 G>C did not map to a codon.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr23:53438751 C>T did not map to a codon.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr23:53438812 C>G did not map to a codon.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr23:53438986 C>G did not map to a codon.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr23:53439088 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr23:53438988 C>T did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr23:53409190 C>G did not map to a codon.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr23:53430748 C>G did not map to a codon.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr23:53432540 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr23:53436093 C>A did not map to a codon.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr23:53432588 C>T did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr23:53432726 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:53432588 C>G did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr23:53441959 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:53409501 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr23:53441780 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr22:45789600 A>G maps to NM_148674.3 N486N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr22:45749909 G>C maps to NM_148674.3 S1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr22:45745646 C>A maps to NM_148674.3 E1153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr22:45789668 C>A maps to NM_148674.3 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr22:45750896 G>A maps to NM_148674.3 N1020N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:106864366 G>T maps to NM_001042550.1 E255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr9:106900436 A>G maps to NM_001042550.1 T1136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:112350862 C>T maps to NM_005445.3 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr3:160137214 C>T maps to NM_005496.3 Q581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr3:160119703 G>A maps to NM_005496.3 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr3:160138553 A>G maps to NM_005496.3 K628K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:72965053 C>T maps to NM_015110.3 R972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr9:72897477 G>A maps to NM_015110.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr9:72892385 C>T maps to NM_015110.3 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr9:72967211 C>A maps to NM_015110.3 R1091R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:17906558 C>A maps to ENST00000381272 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr18:2697899 G>A maps to NM_015295.2 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr18:2697887 C>T maps to NM_015295.2 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr18:2740729 C>T maps to NM_015295.2 Q1182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr18:2688389 A>G did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr18:2772300 G>A maps to NM_015295.2 L1702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr18:2732261 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr18:2762209 C>A maps to NM_015295.2 V1514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr18:2770086 G>A maps to NM_015295.2 Q1649Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr17:18167606 G>A maps to NM_148886.1 E309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr22:39908306 C>G maps to NM_019008.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr22:39909601 C>T maps to NM_019008.4 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr22:39908023 C>T maps to NM_019008.4 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr17:18220825 G>T maps to NM_144775.2 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr17:18219384 C>T maps to NM_144775.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr17:18219699 G>A maps to NM_144775.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr14:91927951 C>A did not map to a codon.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr2:55826171 G>A maps to NM_001122964.1 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr2:55844391 G>A maps to NM_001122964.1 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr2:55825917 T>A maps to NM_001122964.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr2:55806842 G>C maps to NM_001122964.1 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr16:18849688 G>T maps to ENST00000389467 S2395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr16:18860575 C>A maps to ENST00000389467 V1862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr16:18877966 G>C maps to ENST00000389467 S1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr16:18849752 G>A maps to ENST00000389467 R2374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr16:18856888 G>A maps to ENST00000389467 I2027I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:18864944 C>T maps to ENST00000389467 T1576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr16:18847399 G>A maps to ENST00000389467 L2638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr16:18877944 C>T maps to ENST00000389467 G1116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr1:156228843 C>T maps to NM_015327.2 Q798Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:156230277 A>G maps to NM_015327.2 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:156247730 G>A maps to NM_015327.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr1:156242174 G>A maps to NM_015327.2 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:156230256 G>C maps to NM_015327.2 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:156228888 G>T maps to NM_015327.2 I783I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:156228930 G>A maps to NM_015327.2 I769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:156236064 A>G maps to NM_015327.2 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:2202597 G>A maps to NM_017575.4 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:2202363 G>C maps to NM_017575.4 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr1:183486952 C>T maps to ENST00000367537 Q147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:183506338 C>G maps to ENST00000367537 S451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr1:183521064 G>A maps to ENST00000367537 *1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:112058422 G>C maps to NM_005871.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr10:112053928 G>A maps to NM_005871.3 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr7:128850353 G>A maps to NM_005631.4 K539K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr7:128846179 C>T maps to NM_005631.4 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr14:70490102 G>T maps to NM_001034852.1 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr14:70418940 C>A maps to NM_001034852.1 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr6:168910761 C>T maps to NM_022138.2 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr6:169064770 G>T maps to NM_022138.2 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr20:4162526 C>T maps to ENST00000443211 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr20:4162550 C>T maps to ENST00000443211 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:6412142 G>A maps to NM_000543.4 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:109762652 G>A maps to NM_003080.2 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr6:109765032 C>T maps to NM_003080.2 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr16:68395553 G>A maps to NM_018667.3 I606I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr16:68405223 C>T maps to NM_018667.3 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr2:130911283 C>T maps to NM_017951.4 Q667Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:130911410 G>C maps to NM_017951.4 S625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr2:130910918 G>A maps to NM_017951.4 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:130931229 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr2:130912762 G>A maps to NM_017951.4 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:123124902 G>A maps to NM_006714.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr1:28280970 G>A maps to NM_014474.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:28285288 C>G maps to NM_014474.2 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr23:21985321 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr22:31487083 C>T maps to ENST00000454496 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr22:31486842 C>T maps to ENST00000454496 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr22:31493041 G>A maps to ENST00000454496 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr11:57314090 C>A maps to ENST00000457912 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr11:57311164 G>A maps to ENST00000457912 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:57313801 C>A maps to ENST00000457912 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr11:57310112 G>C did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:4498616 C>T maps to NM_001114974.1 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr9:33071778 G>A maps to NM_018225.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:54576209 G>C maps to NM_014311.1 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr7:98634776 G>A maps to NM_020429.2 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr7:98649957 G>A maps to NM_020429.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr7:98639809 G>A maps to NM_020429.2 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:98649873 C>T maps to NM_020429.2 Q225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:62553749 G>T maps to NM_022739.3 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:62553824 G>C maps to NM_022739.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:62589691 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:88405959 C>A maps to NM_198274.3 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr1:214491426 C>A maps to NM_020197.2 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:1703232 C>T maps to NM_052928.2 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr17:1703352 G>C maps to NM_052928.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:1704168 G>A maps to NM_052928.2 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr2:73441447 C>T maps to NM_006062.2 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr2:73447859 C>T maps to NM_006062.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr2:73446020 G>A maps to NM_006062.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr8:49832848 G>A maps to NM_003068.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr8:49832452 A>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr16:88747733 G>A maps to NM_178310.3 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:21242112 C>T maps to NM_004782.3 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr1:227947043 G>A maps to NM_053052.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr1:227923157 G>A maps to NM_053052.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:227923157 G>A maps to NM_053052.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:84311051 G>C maps to NM_014841.2 S421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr14:62229255 C>T maps to NM_003082.3 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr14:62229255 C>T maps to NM_003082.3 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:7986933 G>A maps to NM_003083.3 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:7986330 C>G maps to NM_003083.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:7987342 C>A maps to NM_003083.3 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr19:7987035 C>T maps to NM_003083.3 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr9:139273743 G>C maps to NM_003086.2 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr9:139273422 G>A maps to NM_003086.2 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr9:139276291 G>A maps to NM_003086.2 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr9:139277970 C>T maps to NM_003086.2 A550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr9:139279207 C>A maps to NM_003086.2 E462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr9:139279208 C>T maps to NM_003086.2 E461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr9:139286435 T>C maps to NM_003086.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr1:153633683 G>A maps to NM_012437.4 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:121786335 T>A maps to ENST00000379533 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:121758692 G>A maps to ENST00000379533 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr5:121786477 C>T maps to ENST00000379533 Q693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr5:121767722 G>A maps to ENST00000379533 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr5:121780283 C>T maps to ENST00000379533 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:127714729 G>A maps to NM_014390.2 Q652Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr7:127732071 C>T maps to NM_014390.2 R899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr7:127341353 C>G maps to NM_014390.2 S189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:127544798 G>A did not map to a codon.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr7:127569276 C>T maps to NM_014390.2 Q522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr2:241969870 C>T maps to NM_001080437.1 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr2:242007232 C>A maps to NM_001080437.1 S1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr2:241974124 C>T maps to NM_001080437.1 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr17:47013599 C>T maps to NM_007241.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:47013601 G>A maps to NM_007241.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:47014388 C>T maps to NM_007241.2 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr17:47010656 G>A maps to NM_007241.2 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:38003555 G>A maps to NM_024700.2 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:1286490 C>T maps to ENST00000381876 I470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr20:1286300 C>G maps to ENST00000381876 S407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr20:1285968 G>A maps to ENST00000381876 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr3:43388915 C>T maps to NM_017719.4 Q389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr3:43384955 C>T maps to NM_017719.4 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr3:43389637 C>G maps to NM_017719.4 P629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr3:43389028 G>T maps to NM_017719.4 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:43381799 G>A maps to NM_017719.4 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:96952860 G>A maps to NM_014014.3 I1174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:96955030 C>T maps to NM_014014.3 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:96943980 C>G maps to NM_014014.3 L1868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr2:70123607 C>T maps to NM_006857.1 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:31762254 G>C maps to ENST00000446633 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr19:49589799 G>A maps to NM_003089.4 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr19:49604706 G>T maps to NM_003089.4 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr19:41268861 G>A maps to NM_004596.4 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr19:41265360 C>G maps to NM_004596.4 S91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:41265496 T>A maps to NM_004596.4 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr19:41257378 G>A maps to NM_004596.4 K22K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr20:2444494 G>A maps to ENST00000339610 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr20:2446384 G>C maps to ENST00000339610 S79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr20:16719530 C>G maps to NM_198220.2 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr19:46190951 C>T maps to NM_004597.5 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr19:46190867 G>A maps to NM_004597.5 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr19:46191730 G>C maps to NM_004597.5 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr19:46191817 G>T maps to NM_004597.5 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr2:70515287 A>T maps to NM_003096.2 L31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr20:32026722 C>G maps to NM_003098.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:32005553 C>T maps to NM_003098.2 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr20:32000112 G>C maps to NM_003098.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:32026803 G>C maps to NM_003098.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr16:69334793 G>A maps to NM_006750.3 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr8:51415411 C>G maps to NM_018967.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr8:51569548 G>A maps to NM_018967.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr8:51621489 C>T maps to NM_018967.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr8:51314786 T>A maps to NM_018967.2 C15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr8:51415427 G>T maps to NM_018967.2 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr2:1241710 C>T maps to NM_018968.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr2:1094083 G>T maps to NM_018968.3 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:1271231 C>T maps to NM_018968.3 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:1168817 C>T maps to NM_018968.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:1204826 G>T maps to NM_018968.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr15:25213156 C>T maps to NM_022804.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr15:25213156 C>T maps to NM_022804.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr14:78184463 G>A maps to NM_012245.2 H526H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr14:78187151 C>A maps to NM_012245.2 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:70288044 G>A did not map to a codon.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr23:70282784 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:86256944 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:86253326 T>C maps to NM_153816.3 Q420Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr6:86227734 T>C maps to NM_153816.3 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr11:64802361 A>G maps to NM_013306.4 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:82714734 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr8:82751844 A>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr8:82751897 A>G maps to NM_152836.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr2:27598377 G>C maps to NM_014748.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr5:53839069 G>A maps to NM_001102575.1 Q561Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:53814729 C>T maps to NM_052870.2 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr5:53815260 C>T maps to NM_052870.2 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr5:53815452 G>A maps to NM_052870.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr5:53814456 G>A maps to NM_052870.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:130773220 T>C maps to NM_014758.2 E834E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:130785627 G>A maps to NM_014758.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:130785627 G>A maps to NM_014758.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr11:130785627 G>A maps to NM_014758.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr16:50707940 G>A maps to NM_182854.2 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr16:50709817 G>A maps to NM_182854.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr20:44469297 C>T maps to NM_033421.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr15:64446589 G>C maps to NM_024798.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:64445457 G>A maps to NM_024798.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr15:64446166 C>T maps to NM_024798.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:64445856 G>A maps to NM_024798.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr4:186278862 C>T maps to NM_031953.2 Q711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr4:186180200 G>C maps to NM_031953.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:12172723 C>T maps to NM_001080530.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr6:108581966 G>A maps to NM_003795.4 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:115598510 G>A maps to NM_001012994.1 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr9:115600916 C>T maps to NM_001012994.1 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr9:115598579 G>A maps to NM_001012994.1 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr8:101629925 A>G maps to NM_152628.3 Y118Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr8:101629872 G>C maps to NM_152628.3 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr8:101608875 G>A maps to NM_152628.3 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr8:101608941 G>T maps to NM_152628.3 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr11:65620772 G>A maps to NM_152760.2 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr11:65620763 G>A maps to NM_152760.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr15:75942366 G>C maps to NM_153271.1 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr15:75942837 C>G maps to NM_153271.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr15:75941917 C>A maps to NM_153271.1 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:125166628 C>T maps to NM_003794.2 K449K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr7:2296601 C>T maps to NM_013321.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr7:2311493 G>A maps to NM_013321.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr7:2297420 G>A maps to NM_013321.2 N311N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr7:2317770 G>A maps to NM_013321.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr6:158330749 G>C maps to NM_016224.3 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:179304702 C>T maps to NM_003101.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr1:179316747 C>G maps to NM_003101.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:179310345 C>T maps to NM_003101.4 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr12:53517883 C>A maps to NM_003578.3 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr6:107827517 C>G maps to NM_018013.3 S103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr12:93968537 G>A maps to NM_003877.3 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr17:76354642 C>T maps to NM_003955.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr14:55509990 T>C maps to NM_199421.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr18:67992476 G>A maps to NM_004232.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr18:67992251 G>A maps to NM_004232.3 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr18:67993148 T>C maps to NM_004232.3 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:36523880 C>T maps to NM_014598.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:36522285 C>T maps to NM_014598.2 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:36523814 G>A maps to NM_014598.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr21:33039669 C>T maps to NM_000454.4 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr21:33039653 C>G maps to NM_000454.4 S108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:160105982 G>A maps to NM_000636.2 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr4:24801247 C>T maps to NM_003102.2 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr13:36744694 C>T maps to ENST00000511166 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr13:36744905 G>C maps to ENST00000511166 S417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr16:601634 C>T maps to NM_005632.2 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr16:597449 C>T maps to NM_005632.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr16:602909 G>C maps to NM_005632.2 G984G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr16:601361 G>A maps to NM_005632.2 E709E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:597705 C>T maps to NM_005632.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr21:34932334 C>T maps to NM_032195.1 P2270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr21:34922622 G>A maps to NM_138927.1 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr21:34924455 A>G maps to NM_138927.1 A973A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr21:34926189 T>C maps to NM_138927.1 C1551C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr21:34932412 C>G maps to NM_032195.1 L2296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr10:97174256 C>T maps to NM_001034954.1 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr10:97101149 C>T maps to NM_001034954.1 E854E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr10:97141471 G>T maps to NM_001034954.1 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr4:186570783 G>A maps to ENST00000355634 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr4:186544866 C>A maps to ENST00000355634 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:186544571 G>A maps to ENST00000355634 R767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr4:186545478 G>A maps to ENST00000355634 N464N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr4:186583279 G>C maps to ENST00000355634 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr4:186545478 G>A maps to ENST00000355634 N464N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr4:186544662 G>A maps to ENST00000355634 Y736Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr8:22423914 G>A maps to NM_005775.4 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr8:22423977 C>G maps to NM_005775.4 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr10:108380187 C>A maps to NM_001013031.1 E932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr10:108380188 C>T maps to NM_001013031.1 T931T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:108338852 G>A maps to NM_001013031.1 L1176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr10:108469045 G>A maps to NM_001013031.1 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr10:108923843 C>G maps to NM_001013031.1 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr10:108339125 C>A did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr10:108371674 C>T maps to NM_001013031.1 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr10:108923756 G>T maps to NM_001013031.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr10:108378000 G>T maps to NM_001013031.1 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:7194755 C>A maps to NM_020777.2 S128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr4:7741954 C>T maps to NM_020777.2 I1148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr4:7398028 G>C maps to NM_020777.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr4:7668849 G>T did not map to a codon.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr10:106916943 C>T maps to NM_014978.1 Q511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:106737172 G>A maps to NM_014978.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr10:107022190 C>T maps to NM_014978.1 L1182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr10:106737175 C>T maps to NM_014978.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr10:107022190 C>T maps to NM_014978.1 L1182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr10:106960945 G>A maps to NM_014978.1 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr10:106865233 C>T maps to NM_014978.1 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:106917014 G>C maps to NM_014978.1 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr10:106401695 C>A maps to NM_014978.1 S204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:121460046 G>A maps to NM_003105.5 W1342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:121384942 C>G maps to NM_003105.5 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr11:121414361 C>T maps to NM_003105.5 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr11:121437718 C>A maps to NM_003105.5 C1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr11:121348869 C>G maps to NM_003105.5 S149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr11:121391504 G>T maps to NM_003105.5 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr11:121424811 C>T maps to NM_003105.5 V811V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:121461753 C>T maps to NM_003105.5 L1420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr11:121448044 C>A maps to NM_003105.5 R1172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr11:121437782 C>T maps to NM_003105.5 Q1062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr11:121340813 G>A maps to NM_003105.5 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr11:121424662 C>T maps to NM_003105.5 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:109865576 G>C maps to NM_002959.4 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr1:109867590 G>A maps to NM_002959.4 F588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:109870155 G>C maps to NM_002959.4 S480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr2:39250311 G>A maps to NM_005633.3 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr14:50671061 C>G maps to NM_006939.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr14:50625364 C>T did not map to a codon.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr14:50671079 G>A maps to NM_006939.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr7:16502517 G>T maps to ENST00000396652 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr7:16502463 G>C maps to ENST00000396652 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr13:112722160 C>T maps to NM_005986.2 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr13:112722278 G>T maps to NM_005986.2 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr22:38369568 G>C maps to NM_006941.3 S445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr20:306652 G>T maps to NM_006943.2 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:7492784 C>T maps to NM_006942.1 Q70Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr8:55372533 C>T maps to NM_022454.3 Y408Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr23:139586711 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr5:157078939 C>T maps to NM_178424.1 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr6:21596102 C>T maps to NM_003107.2 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:21595157 G>A maps to NM_003107.2 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:23999031 C>T maps to NM_006940.4 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr12:23757350 C>T maps to NM_006940.4 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:23793808 C>T maps to NM_006940.4 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr12:23887623 C>T maps to NM_006940.4 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr12:23793805 G>T maps to NM_006940.4 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr12:23887620 G>T maps to NM_006940.4 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr11:16007850 C>T maps to NM_001145819.1 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr11:15994389 C>A maps to NM_001145819.1 E831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr8:10584168 C>T maps to ENST00000354846 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr16:1034821 C>T maps to NM_014587.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:1034809 G>T maps to NM_014587.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr16:1034725 G>A maps to NM_014587.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:70119039 C>T maps to NM_000346.3 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr17:70120134 G>T maps to NM_000346.3 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr17:70119894 G>A maps to NM_000346.3 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr17:70119831 G>A maps to NM_000346.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr17:70119708 A>G maps to NM_000346.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:70120203 G>C maps to NM_000346.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:53776402 C>T maps to NM_138473.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:53776784 C>T maps to NM_138473.2 Q352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr12:53776441 C>G maps to NM_138473.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr12:53804988 C>T maps to NM_138473.2 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr12:53776632 C>G maps to NM_138473.2 S301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:53777146 C>T maps to NM_138473.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:53803166 A>G maps to NM_138473.2 K622K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr2:231359152 T>C maps to NM_001080391.1 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr2:231307705 C>T maps to NM_001080391.1 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:231035335 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr2:231081528 T>C maps to NM_080424.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr2:231035452 G>A maps to NM_080424.2 Q638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:231076215 C>T maps to NM_080424.2 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:231079725 G>A maps to NM_080424.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr2:231065643 C>T maps to NM_080424.2 K362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr2:231174705 C>G maps to NM_007237.4 S709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr2:231174715 C>T maps to NM_007237.4 F712F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr2:231118052 C>T maps to NM_007237.4 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:231110621 G>T maps to NM_007237.4 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr2:231174749 G>T maps to NM_007237.4 E724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:45994442 C>T maps to NM_003110.5 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr17:45993796 C>T maps to NM_003110.5 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr17:46000539 G>A maps to NM_003110.5 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr17:45992744 C>A maps to NM_003110.5 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:174820114 C>T maps to NM_003111.4 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr2:174777933 G>C maps to NM_003111.4 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr2:174820675 G>A maps to NM_003111.4 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:171572998 G>A maps to NM_001003845.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr12:53722481 G>A maps to NM_001173467.1 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:53722169 C>T maps to NM_001173467.1 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr12:53722331 G>A maps to NM_001173467.1 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr12:53722238 G>C maps to NM_001173467.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr11:124564317 T>C maps to NM_017425.3 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr6:88775898 G>T did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:31318968 C>T maps to NM_173847.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr17:31322620 C>T maps to NM_173847.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr17:31322625 C>T maps to NM_173847.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:31324481 C>T maps to NM_173847.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr19:49110465 C>T maps to NM_133498.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr8:101243456 C>T maps to NM_003114.3 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr8:101252721 C>A maps to NM_003114.3 S791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr8:101252920 G>A maps to NM_003114.3 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr8:101206368 G>C maps to NM_003114.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:214174841 C>T maps to NM_024532.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:215275024 C>T maps to NM_024532.3 R628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr2:214972960 C>T maps to NM_024532.3 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:214149336 C>T maps to NM_024532.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:214794832 C>G maps to NM_024532.3 S455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr2:215275014 C>T maps to NM_024532.3 D624D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr1:118623859 A>C maps to NM_206996.2 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:118535109 C>G maps to NM_206996.2 L1780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:118640298 C>T maps to NM_206996.2 E335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr1:118537063 G>T maps to NM_206996.2 R1715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:118624182 T>C maps to NM_206996.2 K615K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr1:118598500 A>G maps to NM_206996.2 D859D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:118644396 C>G maps to NM_206996.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr1:118609444 G>A maps to NM_206996.2 V821V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr20:34208865 C>T maps to NM_003116.1 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr20:34208664 G>A maps to NM_003116.1 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr17:26913501 G>A maps to NM_006461.3 Q485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:26906503 C>G did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr17:4863784 G>A maps to NM_004890.2 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr9:35809935 C>T maps to NM_001039592.1 *486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr17:49156969 C>T maps to ENST00000376407 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr17:49067227 C>A maps to ENST00000376407 E876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:49118939 C>T maps to ENST00000376407 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr17:49197843 C>A maps to ENST00000376407 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr17:49071167 G>A maps to ENST00000376407 F786F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:123594194 G>T maps to NM_001174046.1 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr7:123594166 C>G maps to NM_001174046.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr7:123599812 C>G maps to NM_001174046.1 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr23:140336532 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr23:140785778 T>C did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr23:140785772 G>A did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr23:144337273 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr23:142803758 C>G did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:142803726 C>A did not map to a codon.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr23:142795456 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr23:142803686 C>G did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr23:142596839 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:142596844 C>A did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr23:142596961 G>T did not map to a codon.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr23:142605141 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:142596827 A>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:142113829 G>T did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:52825555 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:88394927 C>G maps to NM_004684.4 *665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr4:88414988 G>A maps to NM_004684.4 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr4:88400730 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr2:32352057 C>G maps to NM_014946.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:32340841 G>A maps to NM_014946.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:32289085 G>C maps to NM_014946.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:32339757 C>A maps to NM_014946.3 S245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr3:57107938 C>T maps to NM_181727.1 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:172643145 C>G maps to NM_031955.5 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:217915424 C>T maps to NM_138796.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr1:217915358 G>A maps to NM_138796.2 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:218036152 C>G maps to NM_138796.2 S348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr4:52917884 G>A maps to NM_145263.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr20:48523169 C>T maps to NM_006038.3 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr20:48522406 G>A maps to NM_006038.3 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr17:48629533 G>A maps to NM_022827.2 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:48632591 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr17:48629482 C>T maps to NM_022827.2 G633G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr17:48628893 T>C maps to NM_022827.2 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr17:48628220 C>T maps to NM_022827.2 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr17:48631804 C>T maps to NM_022827.2 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr17:48627415 G>A maps to NM_022827.2 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr1:16731546 C>T maps to NM_198546.1 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:16736160 C>G maps to NM_198546.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr1:16736406 C>T maps to NM_198546.1 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr17:3343611 C>T maps to NM_001170695.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr16:89764653 C>A maps to NM_152339.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr4:177109345 G>A maps to NM_144644.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr4:177116566 G>T maps to NM_144644.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr4:123855675 A>G maps to NM_145207.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr4:123900542 T>G did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr15:45713303 C>T maps to NM_024063.2 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr15:45695569 C>T maps to NM_024063.2 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:48918749 G>A maps to NM_019073.2 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:48825412 G>A maps to NM_019073.2 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr14:88883076 G>A maps to NM_018418.4 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:88862530 G>T maps to NM_018418.4 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr15:97327409 C>A maps to NM_173499.3 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:95011139 C>T maps to NM_031952.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr8:145095889 G>A maps to NM_198572.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:44310890 C>G maps to NM_145026.3 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr6:44336194 C>T maps to NM_145026.3 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:49890686 C>T maps to NM_023071.3 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:49888629 C>A maps to NM_023071.3 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:201342725 C>G maps to ENST00000409151 S558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:201305421 C>T maps to ENST00000409151 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:201332061 C>A maps to ENST00000409151 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr19:11258786 G>T maps to NM_182513.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:11266437 G>A maps to NM_182513.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr2:169732630 A>G maps to NM_020675.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr4:177241292 C>T maps to NM_021928.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr2:29038981 G>A maps to NM_182756.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr11:64939958 T>C maps to NM_001008778.1 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr11:64940162 A>T maps to NM_001008778.1 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr7:44047098 C>T maps to NM_175064.2 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr7:99917268 T>C maps to NM_001004351.4 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr17:8659710 C>T maps to NM_001128076.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr20:3758957 C>T maps to NM_015417.4 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr20:3759866 C>T maps to NM_015417.4 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr5:35697823 A>C maps to NM_024867.3 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:35691332 T>G maps to NM_024867.3 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr5:35779430 T>G maps to NM_024867.3 L1477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr5:35727900 C>A maps to NM_024867.3 V1013V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:35697838 G>A maps to NM_024867.3 K695K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr5:35740311 T>C maps to NM_024867.3 L1091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr5:35759758 G>A maps to NM_024867.3 K1186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr2:220337741 C>T maps to NM_005876.4 F1357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:220344838 C>T maps to NM_005876.4 P1773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr2:220353542 C>T maps to NM_005876.4 Y2690Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr2:220326631 C>G maps to NM_005876.4 P823P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr2:220356865 C>T maps to NM_005876.4 D3165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:220342797 G>A maps to NM_005876.4 R1666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:220353256 C>T maps to NM_005876.4 I2632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:220315984 C>T maps to NM_005876.4 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr2:220313014 G>T maps to NM_005876.4 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr2:220326778 G>A maps to NM_005876.4 K872K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:16265920 G>A maps to NM_015001.2 *3665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:16256133 T>C maps to NM_015001.2 Y1133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:16259145 G>A maps to NM_015001.2 L2137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr1:16255495 C>T maps to NM_015001.2 Q921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr1:16260825 G>C maps to NM_015001.2 V2697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr1:16255497 G>A maps to NM_015001.2 Q921Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:16262028 G>A maps to NM_015001.2 V3098V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr1:16258614 C>T maps to NM_015001.2 A1960A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr1:16255002 C>G maps to NM_015001.2 Y756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:16262748 G>A maps to NM_015001.2 K3338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:16258290 C>T maps to NM_015001.2 L1852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr1:16260336 G>A maps to NM_015001.2 L2534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:16265885 C>T maps to NM_015001.2 I3653I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:16247411 A>G maps to NM_015001.2 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:16202985 A>C maps to NM_015001.2 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr13:46287726 C>G maps to NM_152719.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr15:44951439 G>A maps to NM_025137.3 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:44900790 C>A maps to NM_025137.3 E1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr15:44914485 G>A maps to NM_025137.3 F792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr15:44955821 C>G maps to NM_025137.3 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr15:44900704 G>T maps to NM_025137.3 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr15:44943788 G>C maps to NM_025137.3 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr15:44951275 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr13:36909383 G>T maps to NM_001142294.1 S195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:36909156 C>G did not map to a codon.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr13:36878630 G>A maps to NM_001142294.1 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr13:36888364 C>G maps to NM_001142294.1 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr13:36905577 G>C maps to NM_001142294.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr13:36909298 C>T maps to NM_001142294.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr15:65255978 G>A maps to NM_016630.3 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr15:65266962 G>A maps to NM_016630.3 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:89598328 C>G maps to NM_003119.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr16:89620322 C>T maps to NM_003119.2 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr16:89614465 A>G maps to NM_003119.2 G536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:89590444 G>A maps to NM_003119.2 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr16:89620970 G>T maps to NM_003119.2 A727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:89613073 G>A maps to NM_003119.2 R486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:49132305 C>A maps to NM_020126.3 S414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:49132162 C>T maps to NM_020126.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:49131268 G>A maps to NM_020126.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr19:49130976 G>T maps to NM_020126.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr2:228883064 C>T maps to NM_001142644.1 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr2:228883151 C>T maps to NM_001142644.1 K806K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:228882209 C>G maps to NM_001142644.1 S1120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:228881141 C>T maps to NM_001142644.1 V1476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:228883229 C>T maps to NM_001142644.1 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:228881822 C>T maps to NM_001142644.1 L1249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr2:228882089 C>G maps to NM_001142644.1 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr2:228884725 T>A maps to NM_001142644.1 K282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:50926887 G>A maps to NM_003121.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr9:91090080 G>A maps to NM_006717.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:57162618 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:57021091 C>G did not map to a codon.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr23:57021211 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr23:57020846 T>C did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:57021019 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr23:62570436 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr23:62570095 C>A did not map to a codon.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr23:62570454 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr9:33245128 A>G maps to ENST00000379725 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:147503467 C>T maps to NM_001127698.1 R871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr5:147506617 C>T maps to NM_001127698.1 D1010D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr5:147449903 C>T maps to NM_001127698.1 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr5:147470784 T>A maps to NM_001127698.1 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:147715196 C>G maps to NM_001040433.1 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr20:44170783 C>A maps to NM_020398.3 *134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr20:44175954 G>T maps to ENST00000396669 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr15:41137012 C>T maps to NM_181642.2 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr15:41148492 G>A maps to NM_181642.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr15:41149125 G>T maps to NM_181642.2 E515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr15:41146089 G>A maps to NM_181642.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:38782644 G>A maps to NM_021102.3 *253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr19:38781186 G>A maps to NM_021102.3 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr18:12512467 C>T maps to NM_001128626.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr18:12493152 G>C maps to NM_001128626.1 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr18:12512521 C>T maps to NM_001128626.1 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr16:89934617 C>T maps to NM_032451.1 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr16:89929915 G>C maps to NM_032451.1 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:89922054 C>T maps to NM_032451.1 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr16:89924851 G>T maps to NM_032451.1 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:89929888 C>T maps to NM_032451.1 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr16:89929897 C>A maps to NM_032451.1 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:29675229 C>T maps to NM_003123.3 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr17:4434015 C>G maps to NM_001124758.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr17:4389822 G>C maps to NM_182538.4 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:4349437 G>A maps to NM_182538.4 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr20:55905016 A>C maps to ENST00000371258 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:32264126 G>T maps to NM_144569.4 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr1:32256677 C>T maps to NM_144569.4 L1059L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:32257897 A>T maps to NM_144569.4 S960S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:32257927 G>T maps to NM_144569.4 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:32257939 G>A maps to NM_144569.4 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:167921548 G>A maps to NM_016950.2 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:14280907 G>A maps to NM_006108.2 E524E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:14284331 C>T maps to NM_006108.2 R690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr11:14157021 C>T maps to NM_006108.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr17:47699429 C>A did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr17:47700112 C>T maps to NM_003563.3 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:139308577 C>T maps to NM_001001664.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr2:139326580 C>T maps to NM_001001664.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr15:51041037 G>A maps to NM_032802.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr15:51012138 G>A maps to NM_032802.3 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr19:2351573 G>A maps to NM_152988.2 W498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:2339821 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:2344615 C>T maps to NM_152988.2 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr12:121205361 C>A maps to NM_139015.3 G270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:121205311 G>A maps to NM_139015.3 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr15:38643843 G>C maps to NM_152594.2 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:38614539 G>T maps to NM_152594.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr19:38881043 C>T maps to NM_001042522.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:152957768 G>A maps to NM_005987.3 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:153122433 G>A maps to NM_001014291.3 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:152975690 C>T maps to NM_005416.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:152944473 G>A maps to NM_173080.1 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:152944533 G>A maps to NM_173080.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr4:124322845 C>T maps to NM_199327.1 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr13:80911204 C>T maps to NM_005842.2 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr23:155003686 G>C did not map to a codon.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr23:155004260 G>A did not map to a codon.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr23:155004067 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr12:53468948 G>A maps to NM_032840.2 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:53471014 G>A maps to NM_032840.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr12:53471026 C>T maps to NM_032840.2 K14K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr11:55658696 A>G maps to NM_032681.3 Q316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr11:55653113 G>A maps to NM_032681.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr11:55653303 G>T maps to NM_032681.3 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:6981921 C>T maps to NM_032641.3 W48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr12:6981996 G>C maps to NM_032641.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr16:1828496 G>A maps to NM_080861.3 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr1:158589082 G>C maps to NM_003126.2 V2153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr1:158596662 G>A maps to NM_003126.2 F1933F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr1:158604371 A>T maps to NM_003126.2 A1842A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr1:158647530 C>G maps to NM_003126.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:158645974 A>T maps to NM_003126.2 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:158590241 G>A maps to NM_003126.2 F2045F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:158615286 G>A maps to NM_003126.2 Q1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:158589082 G>C maps to NM_003126.2 V2153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:158644377 T>C maps to NM_003126.2 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr1:158647620 A>G maps to NM_003126.2 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr1:158632504 A>T maps to NM_003126.2 T817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr9:131394414 C>T maps to NM_001130438.2 Q2258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr9:131345411 C>T maps to NM_001130438.2 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr9:131345391 C>T maps to NM_001130438.2 Q615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr9:131388154 C>T maps to NM_001130438.2 I2059I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr9:131356498 G>A maps to NM_001130438.2 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr9:131356541 G>T maps to NM_001130438.2 E1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr9:131351150 C>T maps to NM_001130438.2 Q979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47S-01A-11D-A23U-08 chr9:131337055 C>T maps to NM_001130438.2 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr9:131388959 C>A maps to NM_001130438.2 I2190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr9:131386672 G>T maps to NM_001130438.2 E1967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr9:131339474 C>T maps to NM_001130438.2 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr9:131346652 C>T maps to NM_001130438.2 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr9:131347040 C>T maps to NM_001130438.2 Q827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr9:131329129 T>C maps to NM_001130438.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr9:131387391 G>A maps to NM_001130438.2 E2001E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr9:131342007 G>A maps to NM_001130438.2 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WY-01A-11D-A22Z-08 chr9:131371449 G>T maps to NM_001130438.2 E1549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr9:131362390 G>A maps to NM_001130438.2 W1192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr9:131351140 C>G maps to NM_001130438.2 L975L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr9:131377918 G>A maps to NM_001130438.2 L1719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr9:131339208 G>T maps to NM_001130438.2 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr9:131348124 G>T maps to NM_001130438.2 E887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:131369931 G>T maps to NM_001130438.2 E1366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr9:131340464 G>T maps to NM_001130438.2 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr9:131343205 C>T maps to NM_001130438.2 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr9:131374458 G>A maps to NM_001130438.2 L1659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr9:131378023 C>T maps to NM_001130438.2 I1754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr9:131381221 C>A maps to NM_001130438.2 I1891I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr9:131348069 G>A maps to NM_001130438.2 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr9:131348090 G>A maps to NM_001130438.2 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr9:131386753 G>T maps to NM_001130438.2 E1994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr9:131388256 G>A maps to NM_001130438.2 K2093K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr9:131370490 C>G maps to NM_001130438.2 S1476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr9:131394707 A>G did not map to a codon.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr9:131346673 C>G maps to NM_001130438.2 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr9:131375658 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr9:131339519 C>T maps to NM_001130438.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr14:65253697 C>T maps to ENST00000389723 R999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr14:65260361 G>C maps to ENST00000389723 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:65220340 C>T maps to ENST00000389723 P2176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr14:65251081 C>A maps to ENST00000389723 L1299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr14:65259854 C>T maps to ENST00000389723 Q846Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr14:65268015 G>A maps to ENST00000389723 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:65239525 C>T maps to ENST00000389723 L1779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:54848570 A>T maps to NM_003128.2 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:54874296 G>A maps to NM_003128.2 K1632K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:54882284 C>T maps to NM_003128.2 F1967F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:54843420 G>A maps to NM_003128.2 Q184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr2:54876993 G>A maps to NM_003128.2 K1815K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr2:54880915 C>T maps to NM_003128.2 F1916F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:54826326 C>T maps to NM_003128.2 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:54880909 C>T maps to NM_003128.2 F1914F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:54883056 G>T maps to NM_003128.2 E1990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:54856190 C>T maps to NM_003128.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr2:54891634 G>T maps to NM_003128.2 E2156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:54856385 C>T maps to NM_003128.2 I705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr2:54859865 C>G maps to NM_003128.2 S1243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr2:54856730 G>T maps to NM_003128.2 V820V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr11:66469125 G>T maps to NM_006946.2 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:66460710 C>T maps to NM_006946.2 A1600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:66456632 G>A maps to NM_006946.2 Q1990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr11:66454505 G>C maps to NM_006946.2 V2285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:66458982 G>C maps to NM_006946.2 L1779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr11:66476456 G>C maps to NM_006946.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:66472826 T>C maps to NM_006946.2 S640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr11:66463951 C>G maps to NM_006946.2 L1358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr19:41038641 G>A maps to NM_020971.2 L1353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:41008758 G>A maps to NM_020971.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr19:41009993 C>G maps to NM_020971.2 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr19:41066378 G>A maps to NM_025213.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:41029486 G>C maps to NM_020971.2 L1266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:41008728 A>G maps to NM_020971.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:41012279 C>T maps to NM_020971.2 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr19:41062013 T>G maps to NM_020971.2 S1703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr19:41008180 C>T maps to NM_020971.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr15:42185250 G>A maps to ENST00000320955 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr15:42148609 G>A maps to ENST00000320955 Q2999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:42171660 G>C maps to ENST00000320955 A993A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr15:42170705 G>A maps to ENST00000320955 Q1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr15:42168428 C>T maps to ENST00000320955 L1335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr15:42164021 G>A maps to ENST00000320955 A1753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr15:42170586 C>T maps to ENST00000320955 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr15:42171675 C>G maps to ENST00000320955 L988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr15:42171993 C>G maps to ENST00000320955 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:94809521 G>T maps to NM_006415.2 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr9:94841844 C>T maps to NM_178324.1 *144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr14:78045299 G>A maps to NM_004863.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr14:78023406 G>A maps to NM_004863.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr20:13098329 C>T maps to NM_018327.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr20:13074138 C>G maps to NM_018327.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr20:13074191 C>G maps to NM_018327.2 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr20:13145441 G>A maps to NM_018327.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:18637363 C>A maps to NM_194285.2 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:18636603 G>C maps to NM_194285.2 S406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:18637592 G>C maps to NM_194285.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:18636324 G>C maps to NM_194285.2 S499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr8:126011856 C>G maps to NM_003129.3 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr8:126021217 C>G maps to NM_003129.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr15:45968408 C>A maps to NM_021199.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr15:45968324 C>T maps to NM_021199.2 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr15:45965960 C>T maps to NM_021199.2 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr5:179252155 A>G maps to NM_003900.4 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr5:179263586 G>A maps to NM_003900.4 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr5:179263551 C>T maps to NM_003900.4 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr5:179260684 A>G maps to NM_003900.4 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr5:139930496 C>T did not map to a codon.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr2:45616463 G>A maps to NM_018079.4 L991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:45801776 G>A maps to NM_018079.4 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:45620236 C>A maps to NM_018079.4 E849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:45616463 G>A maps to NM_018079.4 L991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr2:45808902 C>A maps to NM_018079.4 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr20:36031194 C>G maps to ENST00000373558 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr16:30718976 C>T maps to NM_006662.2 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr16:30720938 C>T maps to NM_006662.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:30735079 C>T maps to NM_006662.2 T1445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:30740402 C>T maps to NM_006662.2 F1925F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr16:30744637 C>G maps to NM_006662.2 L2055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr16:30744966 C>T maps to NM_006662.2 F2114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:30734043 C>T maps to NM_006662.2 L1289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:30732143 C>G maps to NM_006662.2 S1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:30732200 C>G maps to NM_006662.2 S1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr16:30740696 C>T maps to NM_006662.2 I1977I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:30727751 C>T maps to NM_006662.2 F923F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr17:36714484 C>A maps to NM_025248.2 E727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:76027117 C>T maps to NM_080744.1 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr7:76026973 G>A maps to NM_080744.1 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr7:76026886 G>A maps to NM_080744.1 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr5:6633925 C>T maps to NM_001047.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr2:31754485 C>A maps to NM_000348.3 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr4:56236182 C>T maps to NM_024592.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr22:42263231 G>A maps to NM_004599.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr12:64437273 G>C maps to NM_020762.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr12:64485154 C>G maps to NM_020762.2 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr12:64383737 G>A maps to NM_020762.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr1:206623768 C>G maps to ENST00000414359 S636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:206628298 G>A maps to ENST00000414359 V735V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:206566185 C>T maps to ENST00000414359 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:9055452 C>G maps to NM_014850.2 V629V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:9146372 G>C maps to NM_014850.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr3:9027277 G>A maps to NM_014850.2 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:9146378 G>A maps to NM_014850.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr3:9027541 C>T maps to NM_014850.2 A987A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr3:9106157 G>T maps to NM_014850.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr3:9055434 G>A maps to NM_014850.2 F635F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr7:87839445 C>A did not map to a codon.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr7:87838666 C>T maps to NM_003130.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr16:4242552 G>A maps to ENST00000330063 R779R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr16:4242495 G>A maps to ENST00000330063 F798F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7N-01A-11D-A391-08 chr1:11115108 C>T maps to NM_003132.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr20:62178656 G>A maps to NM_080823.2 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr20:62173799 G>A maps to NM_080823.2 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr14:35497327 G>A maps to NM_003136.3 Q454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr14:35465980 T>A maps to NM_003136.3 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr14:35497300 C>T maps to NM_003136.3 D445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr17:74060233 C>G maps to NM_014230.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:74053482 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:74041407 C>T maps to NM_014230.2 E453E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:74056445 G>A maps to NM_014230.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr4:57367867 G>C maps to NM_006947.3 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr6:35856665 G>A maps to ENST00000361690 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr7:104782914 C>T maps to ENST00000336613 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr7:104909275 A>C maps to NM_182691.1 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr7:104844168 C>T maps to ENST00000336613 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr23:153049815 C>T did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:153050894 C>G did not map to a codon.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr23:153049629 C>T did not map to a codon.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr23:153050965 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:153048312 G>A did not map to a codon.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr23:153047050 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:153047008 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr23:153049756 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:153049657 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:133525480 G>A maps to NM_021203.3 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr23:38019288 G>A did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr23:38020252 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr23:99919816 C>A did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr17:2221249 A>C maps to NM_021947.1 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr17:2221222 G>A maps to NM_021947.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr16:2806514 G>A maps to NM_016333.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr16:2813978 G>A maps to NM_016333.3 S1150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:2812175 G>A maps to NM_016333.3 Q549Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:2812361 G>C maps to NM_016333.3 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:2812686 A>C maps to NM_016333.3 R720R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:2815188 C>T maps to NM_016333.3 Q1554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:2813060 G>A maps to NM_016333.3 V844V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:2819243 C>T maps to NM_016333.3 P2660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:2815127 G>C maps to NM_016333.3 L1533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr16:2812361 G>A maps to NM_016333.3 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr16:2817461 C>T maps to NM_016333.3 L2311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr16:2806577 C>G maps to NM_016333.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr16:2818181 G>C maps to NM_016333.3 S2551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr16:2813315 C>T maps to NM_016333.3 S929S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr16:2815613 G>A maps to NM_016333.3 P1695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr16:2810397 C>T maps to NM_016333.3 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:75890732 G>A did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr12:119559910 G>A maps to NM_194286.2 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:119583319 C>T maps to NM_194286.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr12:119583486 C>G maps to NM_194286.2 S358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr12:119419746 C>T maps to NM_194286.2 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:100483361 C>G maps to NM_015908.5 S453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:100478980 C>T maps to NM_015908.5 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr7:100479364 C>T maps to NM_015908.5 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr7:100485475 C>T maps to NM_015908.5 A774A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:100479835 C>T maps to NM_015908.5 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr18:23612473 A>T maps to ENST00000415083 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:60734977 C>T maps to NM_198935.1 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:170666804 G>T maps to NM_003142.3 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr7:141450135 G>A maps to NM_003143.1 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr5:80911319 G>T maps to ENST00000380182 S85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:54707878 C>A maps to NM_145716.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:54692804 C>T maps to NM_145716.2 *389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr19:18543828 C>T maps to NM_032627.3 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr2:182778576 C>T maps to NM_001130445.1 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:182766800 C>T maps to NM_001130445.1 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr12:109182060 C>T maps to NM_018984.3 V951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr12:109200139 G>A maps to NM_018984.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr17:27959439 C>T maps to NM_033389.2 K897K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:27999020 G>A maps to NM_033389.2 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:27958626 G>A maps to NM_033389.2 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr11:67079349 G>T maps to NM_017857.3 E658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr11:67079356 G>C maps to NM_017857.3 *660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:67075643 G>T did not map to a codon.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr11:67077410 C>T maps to NM_017857.3 Q461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr11:67077776 G>A maps to NM_017857.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:67074847 C>T maps to NM_017857.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:140083656 G>A maps to NM_003731.2 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr9:140083593 G>A maps to NM_003731.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr9:140083665 T>C maps to NM_003731.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr12:26377227 C>G maps to NM_005086.4 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr12:26383789 G>A maps to NM_005086.4 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr7:149477947 C>T maps to NM_198455.2 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr7:149492423 C>T maps to NM_198455.2 Q2106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr7:149524941 A>G maps to NM_198455.2 T4956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr7:149482089 G>A maps to NM_198455.2 Q960Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:149498954 G>A maps to NM_198455.2 L2470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr7:149497501 C>T maps to NM_198455.2 S2421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr7:149494389 C>G maps to NM_198455.2 L2288L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-XF-A9T0-01A-11D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr7:149523590 C>T maps to NM_198455.2 L4840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr7:149484616 C>T maps to NM_198455.2 L1181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr7:149483201 G>A maps to NM_198455.2 V1091V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr1:155989829 C>T maps to ENST00000368312 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:156271469 C>T maps to ENST00000467789 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr11:57100510 G>A maps to NM_003146.2 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr11:57095839 C>T maps to NM_003146.2 E514E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr14:38678914 C>A maps to NM_001049.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:38679238 C>T maps to NM_001049.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr14:38678851 T>C maps to NM_001049.2 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr14:38678980 C>G maps to NM_001049.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr14:38679280 C>G maps to NM_001049.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr17:71166024 G>A maps to NM_001050.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr17:71165502 A>G maps to NM_001050.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr22:37603236 C>T maps to NM_001051.2 W202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr20:23016437 G>T maps to NM_001052.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr16:1129227 C>T maps to NM_001053.3 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr1:1480339 C>T maps to NM_014188.2 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr23:48117199 C>A did not map to a codon.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr23:48125804 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:85128144 C>A maps to NM_001166417.1 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr23:48214672 A>G did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:48214124 G>C did not map to a codon.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr23:48209003 C>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:48208986 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr23:48054494 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:52681309 C>T did not map to a codon.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr23:52681319 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr23:52682476 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr22:41228586 C>A maps to NM_003932.3 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:130066274 C>T maps to NM_021978.3 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:130066284 G>T maps to NM_021978.3 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr11:130069860 C>G maps to NM_021978.3 S608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr11:130066235 G>C maps to NM_021978.3 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:130068448 G>A maps to NM_021978.3 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:53062371 G>A maps to NM_014682.2 Q658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr8:53084871 C>T maps to NM_014682.2 Q183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr8:53084385 G>A maps to NM_014682.2 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr8:53084640 C>T maps to NM_014682.2 Q260Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr8:134475668 C>T maps to NM_173344.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr8:134477049 C>G maps to NM_173344.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:44360120 C>T maps to NM_174963.2 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:44395889 C>A maps to NM_174963.2 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr11:126278200 G>C did not map to a codon.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr11:126279194 C>T maps to ENST00000356132 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr2:86090486 G>C maps to NM_003896.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr3:98489772 C>G maps to ENST00000493584 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr3:98512580 C>T maps to ENST00000493584 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr11:8720888 G>A maps to NM_005418.3 F923F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr11:8724141 G>C maps to NM_005418.3 V899V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr3:186790662 C>G maps to NM_003032.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:186760991 T>C maps to NM_003032.2 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:186760545 C>T maps to NM_003032.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr3:186793483 C>T maps to NM_003032.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:186793464 G>A maps to NM_003032.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr2:107446555 C>T maps to NM_001142351.1 K428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr17:74625230 G>A maps to NM_018414.3 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr17:74639590 T>G maps to NM_018414.3 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr17:74569326 C>T maps to NM_006456.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:76877754 G>A maps to NM_152996.2 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:77093182 C>T maps to NM_152996.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr1:76878069 T>C maps to NM_152996.2 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr1:77509893 G>A maps to NM_030965.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr7:116849887 G>A maps to ENST00000323984 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr7:116759718 C>A maps to ENST00000323984 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr7:116869838 C>G maps to ENST00000323984 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:113159452 C>T maps to NM_017744.4 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr12:22354790 G>A maps to NM_003034.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr12:22487046 G>T maps to NM_003034.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7N-01A-11D-A391-08 chr15:92973290 C>G maps to NM_006011.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:93007599 C>T maps to NM_006011.3 C371C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr15:92987952 G>T maps to NM_006011.3 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr15:93007521 G>A maps to NM_006011.3 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr18:55027261 G>A maps to NM_015879.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr5:100191823 A>C maps to NM_005668.4 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr18:44260397 C>T maps to NM_013305.4 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr18:44260222 G>A maps to NM_013305.4 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr18:44260142 G>C maps to NM_013305.4 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:17363212 G>A maps to NM_001004470.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr10:17363116 G>A maps to NM_001004470.1 Y319Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr10:17362909 G>C maps to NM_001004470.1 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr10:17363161 C>A maps to NM_001004470.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:52557549 C>T maps to NM_015136.2 I2416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr3:52552853 C>G maps to NM_015136.2 S1668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr3:52549519 C>T maps to NM_015136.2 Q1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:52529473 C>T maps to NM_015136.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr3:52554413 A>T did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr3:52553377 C>T maps to NM_015136.2 P1711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr12:104067769 C>A maps to NM_017564.9 A819A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:104098376 C>T maps to NM_017564.9 F1295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:104121064 G>C maps to NM_017564.9 L1624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr12:104044295 G>A maps to NM_017564.9 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:104049331 C>A maps to NM_017564.9 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr12:104152951 C>T maps to NM_017564.9 V2383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr12:104156095 C>T maps to NM_017564.9 I2468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr12:104152922 C>A maps to NM_017564.9 R2374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:36587729 C>T maps to NM_003149.1 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr3:36547282 T>C maps to NM_003149.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr3:36527674 C>T maps to NM_003149.1 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr17:37374336 G>C maps to NM_198993.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:57638145 T>A maps to NM_145064.1 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr12:57637893 G>A maps to NM_145064.1 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr12:57637671 C>A maps to NM_145064.1 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr12:57638327 C>G maps to NM_145064.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr3:136088079 T>C maps to NM_005862.2 Q805Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:136287646 C>T maps to NM_005862.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr3:136170919 A>G maps to NM_005862.2 N461N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr3:136192461 C>T maps to NM_005862.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr3:136323192 G>C maps to NM_005862.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:136085924 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr3:136342047 G>A maps to NM_005862.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:136062720 A>T maps to NM_005862.2 I1133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr23:123196801 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr23:123205033 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr23:123205141 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr23:123202444 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr23:123220455 G>A did not map to a codon.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr23:123200038 C>T did not map to a codon.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr23:123197010 C>T did not map to a codon.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr23:123217379 C>T did not map to a codon.
Sequencing variant TCGA-CF-A47W-01A-11D-A23U-08 chr23:123202464 C>T did not map to a codon.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr23:123227961 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr23:123190028 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr23:123179196 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr23:123197010 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:123179196 C>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:123195141 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr23:123179196 C>T did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:123182852 A>C did not map to a codon.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr23:123196750 G>A did not map to a codon.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr23:123197010 C>T did not map to a codon.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr23:123179196 C>T did not map to a codon.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr23:123171454 C>T did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr23:123210186 C>T did not map to a codon.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr23:123179173 C>A did not map to a codon.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr23:123190074 C>T did not map to a codon.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr23:123215340 C>T did not map to a codon.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr23:123179209 C>T did not map to a codon.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr23:123202474 T>C did not map to a codon.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr23:123200109 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr23:123185060 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr23:123176494 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr23:123195158 T>A did not map to a codon.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr23:123196763 A>T did not map to a codon.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr23:123196822 C>G did not map to a codon.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr23:123197010 C>T did not map to a codon.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr23:123220470 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr23:123220427 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr23:123220519 C>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:123179191 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:123159714 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:123184086 G>A did not map to a codon.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr23:123184054 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr23:123185177 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr23:123185188 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:123217379 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr23:123197010 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:123210197 T>A did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:123210198 G>T did not map to a codon.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr23:123205003 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr23:123190005 G>C did not map to a codon.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr23:123211872 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr23:123224563 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr23:123202461 T>C did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr23:123171441 C>T did not map to a codon.
Alternatively spliced codon TCGA-DK-A2I1-01A-11D-A17V-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr7:99796486 G>A maps to NM_012447.2 E458E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-GU-AATQ-01A-11D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr7:99809156 G>A maps to NM_012447.2 L1170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr7:66770991 C>T maps to NM_022906.2 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr7:66774702 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr10:17730071 G>A maps to NM_003473.2 W115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr10:17730072 G>A maps to NM_003473.2 W115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr10:17750926 G>A maps to NM_003473.2 Q454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr2:153004798 T>C maps to NM_005843.4 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:153006743 C>T did not map to a codon.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr10:90672880 C>G maps to NM_020799.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr4:68447081 C>A maps to NM_012108.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:4333774 G>C maps to ENST00000314714 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr19:4333711 C>A maps to ENST00000314714 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr19:4338735 C>T maps to ENST00000314714 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr19:4333720 C>T maps to ENST00000314714 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr19:4327382 C>T did not map to a codon.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr8:38006216 C>T maps to NM_000349.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:72466775 C>T maps to NM_006645.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr11:72469643 G>A maps to NM_006645.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:33700223 G>C maps to NM_178007.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:37809999 G>C maps to NM_006804.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:37818530 C>T maps to NM_006804.3 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr17:37815023 C>A maps to NM_006804.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr17:37813328 C>T maps to NM_006804.3 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr18:51851179 G>C maps to NM_139171.1 S182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr2:96860704 G>A maps to NM_020151.3 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr2:96852602 C>T maps to NM_020151.3 K326K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr2:96852559 G>A maps to NM_020151.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:67937491 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr23:67940174 A>C did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr23:67940784 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:67938373 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr23:67937194 G>A did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:67937974 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:191854375 C>T maps to NM_007315.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:191841751 C>G did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr2:191840559 C>A maps to NM_007315.3 E705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:191850350 C>T maps to NM_007315.3 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:56749505 G>A maps to NM_005419.3 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr12:56749135 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr12:56744662 C>T maps to NM_005419.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr12:56743000 G>A maps to NM_005419.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:56739937 G>C maps to NM_005419.3 V698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr17:40476995 C>T maps to NM_139276.2 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:40456552 G>A maps to NM_003152.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr17:40456422 C>G maps to NM_003152.3 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr17:40460319 G>A maps to NM_003152.3 E677E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr17:40359699 G>A maps to NM_012448.3 F651F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:40370257 C>T maps to NM_012448.3 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr17:40379651 G>C maps to NM_012448.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr17:40354827 T>G did not map to a codon.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr12:57490851 G>A maps to NM_003153.4 Q742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr4:70866581 T>C maps to NM_003154.2 Y35Y. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-4Z-AA89-01A-11D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr20:47736553 G>A maps to NM_017453.2 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr20:47752381 A>G maps to NM_017453.2 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr20:47733704 G>T maps to NM_017453.2 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr8:74600985 C>T maps to NM_001164380.1 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr4:77230915 C>T maps to NM_003943.3 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr8:23709008 G>A maps to NM_003155.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr8:23708866 C>A maps to NM_003155.2 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr8:23711973 C>T maps to NM_003155.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr5:172744987 A>T maps to NM_003714.2 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:89854698 G>C maps to NM_152999.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr7:89856592 C>G maps to NM_152999.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr7:87913436 G>A maps to NM_024636.2 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr7:87908750 T>G maps to NM_024636.2 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr17:44076785 C>A maps to NM_001007532.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr17:44076765 C>T maps to NM_001007532.2 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr1:47728682 C>A maps to NM_001048166.1 G907G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:47767247 G>A maps to NM_001048166.1 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:47717383 G>C maps to NM_001048166.1 L1097L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:47746037 G>A maps to NM_001048166.1 Q698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr11:3877559 C>G maps to NM_003156.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr11:4045119 C>G maps to NM_003156.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr4:26959235 C>T maps to ENST00000382009 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr4:27024342 C>T maps to ENST00000382009 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:26959235 C>T maps to ENST00000382009 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr4:27009300 G>A maps to ENST00000382009 Q463Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr11:63962053 G>C maps to ENST00000358794 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr11:63961764 G>T maps to ENST00000358794 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr11:63971070 G>A maps to ENST00000358794 Q559Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr11:63971085 A>T maps to ENST00000358794 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr5:171471887 A>C maps to NM_005990.3 *969E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:171517360 C>T maps to NM_005990.3 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr5:171614992 T>C maps to NM_005990.3 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:1223160 C>T maps to NM_000455.4 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr2:220466158 C>G maps to NM_052902.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr2:220470930 G>C maps to NM_052902.2 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr2:220476407 G>C maps to NM_052902.2 R740R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr2:220466131 C>T maps to NM_052902.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:220111531 C>T maps to ENST00000409260 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr2:220113197 C>T maps to ENST00000409260 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr7:43664256 C>A maps to NM_004760.2 S354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr2:197002452 C>T maps to NM_004226.3 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:31940163 C>T maps to NM_032454.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr6:31939892 C>T maps to NM_032454.1 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr13:99171543 G>A maps to NM_003576.3 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr2:242438520 G>C maps to NM_006374.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr2:242441096 G>T maps to NM_006374.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr8:99468129 C>T maps to ENST00000354930 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr8:99761531 G>C maps to ENST00000354930 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr8:99718790 T>A maps to ENST00000354930 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr7:23810676 G>T maps to NM_031414.3 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr7:23775421 C>G maps to NM_031414.3 S250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr7:23810668 C>T maps to NM_031414.3 Q587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr7:23808777 C>T maps to NM_031414.3 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr5:146754651 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:5468468 G>T maps to NM_018401.1 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr4:5399951 T>C maps to NM_018401.1 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr4:5500808 G>C maps to NM_018401.1 *415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr4:5399960 G>T maps to NM_018401.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr4:5332958 G>A maps to NM_018401.1 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T4-01A-11D-A391-08 chr11:8496317 T>A maps to NM_030906.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr20:2097549 C>G maps to NM_080836.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr20:2083811 G>A maps to NM_080836.3 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:219544718 C>G maps to NM_015690.3 S351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr2:219540916 C>T maps to NM_015690.3 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr2:219557992 G>T maps to NM_015690.3 E692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:219562315 G>A maps to NM_015690.3 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr6:36475370 C>T maps to NM_007271.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:36483156 G>A maps to NM_007271.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr6:36507962 G>C maps to NM_007271.2 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:168997163 C>A maps to NM_013233.2 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr20:43625889 G>A maps to NM_006282.2 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr1:36807475 C>A maps to ENST00000373130 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr1:36820992 C>G maps to ENST00000373130 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr8:80553751 G>A maps to NM_007029.3 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr8:80549076 G>A maps to NM_007029.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr8:80577107 G>A maps to NM_007029.3 *180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:62275250 G>C maps to NM_015894.2 S50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr20:62273517 G>C maps to NM_015894.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr20:62273535 G>C maps to NM_015894.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr9:124103552 G>C maps to NM_004099.4 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr9:124110340 C>T maps to NM_004099.4 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr13:39540962 C>T maps to NM_145286.2 *292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr2:48807856 C>T maps to NM_172311.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr2:48808502 C>A maps to NM_172311.2 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr2:48808785 C>T maps to NM_172311.2 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:48808842 A>G maps to NM_172311.2 K357K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr14:81743986 T>C maps to NM_033104.2 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:184930932 C>A maps to NM_020225.1 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:134931192 G>A maps to NM_182489.1 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr7:134939928 C>T maps to NM_182489.1 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:61787957 G>A maps to NM_001003787.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr17:61787906 G>A maps to NM_001003787.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:202339368 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr2:202342853 G>T maps to NM_018571.5 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:16052898 C>T maps to ENST00000025399 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr12:16048297 G>A maps to ENST00000025399 W182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr9:125923294 C>T maps to NM_018387.4 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr9:125923303 C>T maps to NM_018387.4 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr9:125898321 G>A maps to NM_018387.4 Q591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr9:125910116 C>A maps to NM_018387.4 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr9:125941506 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr15:43896297 C>T maps to NM_153700.2 W1424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr14:31364786 C>A did not map to a codon.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr19:47236402 G>A maps to NM_001039877.1 N210N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:7268217 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr23:7268166 G>C did not map to a codon.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr23:7177777 G>C did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr23:7175543 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr23:7268122 G>A did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr23:7268270 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr23:7268038 C>A did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr11:125482605 G>A maps to NM_152713.3 K443K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr3:31638348 C>T maps to NM_178862.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:31574503 C>A maps to NM_178862.1 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr16:732416 C>T maps to NM_005861.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr16:731256 C>T maps to NM_005861.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr16:731219 C>T maps to NM_005861.2 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:13260330 C>G maps to NM_003765.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr19:13260351 C>T maps to NM_003765.1 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr6:144508444 C>G maps to NM_003764.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr6:144508324 C>T maps to NM_003764.3 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr6:144508444 C>G maps to NM_003764.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr20:57251298 C>T maps to NM_001001433.1 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr9:102713544 G>A maps to NM_017919.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr9:102729972 C>T maps to NM_017919.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:102722412 C>T maps to NM_017919.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:93733303 T>C maps to NM_001001850.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr7:73118096 G>A maps to NM_004603.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr7:73114793 G>A maps to NM_004603.3 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr16:31004781 C>T maps to NM_052874.3 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:59554580 C>T maps to NM_004177.4 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr11:59523077 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:31049269 C>T maps to NM_004604.3 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr16:31045558 C>A maps to NM_004604.3 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:62575049 G>C maps to NM_003164.3 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr11:62592763 C>G maps to NM_003164.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr6:132824615 G>A maps to NM_003569.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:9153948 C>T maps to NM_004853.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr9:130416004 G>A maps to NM_003165.3 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:130434371 C>T maps to NM_003165.3 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr9:130425600 C>T maps to NM_003165.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:109339275 G>A maps to NM_007269.2 Q428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr17:53084945 G>A maps to NM_178509.5 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr6:147527159 A>G maps to NM_001127715.1 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr6:147525679 C>T maps to NM_001127715.1 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr6:147704099 C>G maps to NM_001127715.1 S1127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr6:147525745 G>A maps to NM_001127715.1 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr6:147648377 C>T maps to NM_001127715.1 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr6:147684702 C>T maps to NM_001127715.1 I926I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr6:147648323 C>G maps to NM_001127715.1 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:147694883 C>G maps to NM_001127715.1 L1033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr6:147636837 C>T maps to NM_001127715.1 F530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:121132109 C>T maps to NM_014980.2 L1042L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr14:25281915 C>T maps to NM_014178.6 *211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr12:10780302 A>C maps to NM_018423.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr12:10782154 G>A maps to NM_018423.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:10774500 C>T maps to NM_018423.2 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr7:75643143 G>A maps to NM_016086.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr7:75651262 C>T maps to NM_016086.2 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr13:48542733 T>C maps to NM_003850.2 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr3:151599167 G>T maps to NM_033050.4 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:151599260 G>C maps to NM_033050.4 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr10:104357039 C>T maps to NM_016169.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr10:104353767 G>A maps to NM_016169.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr8:70498670 G>A maps to NM_001128206.1 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr8:70517049 T>G maps to NM_001128206.1 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:46292923 G>C maps to NM_001161841.1 T669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr20:46313303 C>T maps to NM_001161841.1 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr20:46290637 C>G maps to NM_001161841.1 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr20:46288162 C>T maps to NM_001161841.1 K854K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr20:46313303 C>T maps to NM_001161841.1 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr20:46294037 C>T did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr16:28603635 G>A maps to NM_001054.3 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:28603659 C>T maps to NM_001054.3 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:28603593 G>A maps to NM_001054.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr16:28604835 G>A maps to NM_001054.3 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr4:70620789 G>C maps to NM_014465.3 S49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr4:70615495 C>T maps to NM_014465.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr2:108881805 G>A maps to NM_001008743.1 *305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr2:108998922 A>T maps to NM_006588.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:108999547 G>C did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:108994855 C>T maps to NM_006588.2 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr19:49090663 C>T maps to NM_177973.1 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr19:49090669 G>A maps to NM_177973.1 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr22:44237732 G>A maps to NM_014351.3 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:37410657 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr2:37402280 C>G maps to NM_001032377.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:4494721 G>A maps to NM_182760.3 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:4494727 G>T maps to NM_182760.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:56141898 A>G maps to ENST00000395437 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:56142307 G>A maps to ENST00000395437 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr7:56147347 G>T maps to NM_001130069.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:203071985 G>C maps to ENST00000409368 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:73164439 G>C maps to NM_006937.3 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:73177190 T>C maps to NM_006937.3 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr21:46233983 C>T maps to ENST00000411651 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr7:899955 C>G maps to ENST00000456758 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr7:894554 A>G did not map to a codon.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr22:39141784 C>T maps to ENST00000405018 Q260Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr22:39144721 C>T maps to ENST00000405018 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr22:39137510 G>A maps to ENST00000405018 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr7:48026959 G>A maps to NM_152782.3 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr7:48068433 G>A maps to NM_152782.3 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr20:31571719 C>T maps to NM_080675.3 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr20:31571698 C>T maps to NM_080675.3 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:56396034 C>T maps to NM_001032387.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:56397730 G>C maps to NM_001032387.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr12:56397517 G>C maps to NM_001032387.1 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr14:21829275 T>C maps to NM_007192.3 K630K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr14:21834656 G>T maps to NM_007192.3 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr14:21852041 C>T maps to NM_007192.3 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr14:21838055 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr14:21828576 G>C maps to NM_007192.3 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr14:21837928 C>A maps to NM_007192.3 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr6:45073658 C>A maps to NM_181356.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr6:44797553 C>G maps to NM_181356.1 *329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr19:39955604 C>G maps to NM_003169.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:39963712 C>A maps to NM_003169.3 T739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:39963871 C>A maps to NM_003169.3 S763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr19:39967026 C>T maps to NM_003169.3 L1084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:39963658 C>T maps to NM_003169.3 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr19:39963694 T>C maps to NM_003169.3 R733R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:27010764 C>T maps to NM_003170.3 F720F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:27028138 C>T maps to NM_003170.3 Q1663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr17:27008290 C>G maps to NM_003170.3 S456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr17:27016512 C>T maps to NM_003170.3 I1092I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr17:27011885 G>T maps to NM_003170.3 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr17:27017146 G>A maps to NM_003170.3 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr17:27014224 C>G maps to NM_003170.3 L940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr2:27880451 G>A maps to NM_014860.1 H168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr2:27884011 C>T maps to NM_014860.1 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr10:70940253 G>A maps to NM_003171.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr10:70968769 G>A maps to NM_003171.3 K780K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr9:136220671 G>A maps to NM_003172.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr9:136218806 C>G maps to NM_003172.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr9:136233519 G>A maps to NM_033161.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr9:136199548 C>T maps to NM_006753.4 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr9:136198950 C>G maps to NM_006753.4 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr9:114860810 C>T maps to NM_022486.3 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr9:114842401 G>T maps to NM_022486.3 C506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:24579486 C>A maps to NM_019601.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:223536709 G>A maps to NM_017982.3 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:223396885 C>G maps to NM_017982.3 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr1:223441985 C>T maps to NM_017982.3 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr1:223465952 G>A maps to NM_017982.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:223402707 C>T maps to NM_017982.3 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:33194714 G>C maps to NM_015551.1 S470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr23:48558637 C>A did not map to a codon.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr23:48564727 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr10:14939476 G>A maps to NM_001193424.1 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr11:67957390 C>T maps to NM_017635.3 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr11:67925717 G>A maps to NM_017635.3 R699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:30302569 C>T maps to NM_015355.2 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr17:30320996 C>G maps to NM_015355.2 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:30267338 G>C maps to NM_015355.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:30315352 C>T maps to NM_015355.2 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr17:30320259 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:149885326 G>T maps to NM_014849.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:149880778 C>G maps to NM_014849.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr15:91809816 C>G maps to NM_014848.4 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:75505590 G>A maps to NM_014979.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr5:75587666 C>T maps to NM_014979.1 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr9:113141678 C>T maps to ENST00000374463 L3455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:113170847 A>G maps to ENST00000374463 V2347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr9:113169861 G>C maps to ENST00000374463 S2676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr9:113192270 A>T maps to ENST00000374463 G1851G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr9:113205984 C>G maps to ENST00000374463 V1493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr9:113168735 G>A maps to ENST00000374463 A3051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr9:113219583 G>A maps to ENST00000374463 Q1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr9:113233659 C>G maps to ENST00000374463 L994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr10:29824925 C>T maps to NM_021738.2 W300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr10:29777620 G>A maps to NM_021738.2 S1419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr10:29820208 G>C maps to NM_021738.2 S673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr10:29752433 G>C maps to NM_021738.2 L2088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr10:29747178 G>A maps to NM_021738.2 F2214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr10:29812497 C>T maps to NM_021738.2 P1015P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr10:29812500 T>C maps to NM_021738.2 E1014E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr10:29819559 G>A maps to NM_021738.2 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr10:29818751 C>A maps to NM_021738.2 E710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr10:29812650 C>T maps to NM_021738.2 E964E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr10:29821653 G>A maps to NM_021738.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr11:22848836 T>C maps to NM_148893.1 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr12:109306433 C>T maps to NM_018711.2 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:138333768 G>A maps to NM_001139456.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:138333771 G>A maps to NM_001139456.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr7:138310791 G>A maps to NM_001139456.1 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr7:138312174 G>A maps to NM_001139456.1 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr7:138341219 G>T maps to NM_001139456.1 Y169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr7:138312123 G>A maps to NM_001139456.1 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr11:9761757 C>T maps to NM_015055.2 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr23:16775341 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr23:16773176 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr8:110592171 G>T maps to NM_001099744.1 S197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr10:135369107 G>T maps to NM_001143764.1 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:135369390 C>G maps to NM_001143764.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr19:13029072 C>A maps to NM_001105578.1 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr19:39694507 G>C maps to NM_001080468.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr1:115454197 C>T maps to NM_003176.2 N508N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:58467367 T>A maps to NM_014258.2 K681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr20:58450464 G>A maps to NM_014258.2 V1070V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr20:58482421 C>A maps to NM_014258.2 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr6:10956471 T>A maps to NM_001040274.2 Y720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:10891744 G>C did not map to a codon.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr6:10956417 T>A maps to NM_001040274.2 G702G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr19:15224635 C>A maps to NM_033025.4 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:85634732 A>G maps to NM_032184.1 I949I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr1:85648703 G>A maps to NM_032184.1 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr9:93636993 C>T maps to NM_003177.5 Y348Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr9:93629437 C>G maps to NM_003177.5 S291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr9:93637075 G>T maps to NM_003177.5 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr9:93606488 C>T maps to NM_003177.5 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr9:93650065 C>T maps to NM_003177.5 Y539Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr9:93607846 G>C maps to NM_003177.5 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr19:46345717 G>A maps to NM_004819.2 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr19:46341739 C>T maps to NM_004819.2 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr19:46332274 G>A maps to NM_004819.2 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:46347366 C>G maps to NM_004819.2 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr23:47464457 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:47478940 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:47466406 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr22:32924938 C>T maps to NM_003490.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr6:152639224 C>T maps to NM_182961.2 K5521K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr6:152523044 C>A maps to NM_182961.2 E7687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:152640036 C>T maps to NM_182961.2 A5450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr6:152771878 G>A maps to NM_182961.2 D1092D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr6:152461087 G>C maps to NM_182961.2 L8485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr6:152675919 C>T maps to NM_182961.2 L3600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:152651319 G>A maps to NM_182961.2 R4834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:152651533 C>T maps to NM_182961.2 L4762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:152737549 C>A maps to NM_182961.2 E2008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr6:152651956 C>T maps to NM_182961.2 T4621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr6:152690228 G>A maps to NM_182961.2 Q3229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr6:152690228 G>A maps to NM_182961.2 Q3229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr6:152792773 G>A maps to NM_182961.2 Y530Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr6:152737711 G>A maps to NM_182961.2 Q1954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr6:152690737 G>T maps to NM_182961.2 I3173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr6:152477103 C>T maps to NM_182961.2 T7973T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr6:152551704 G>A maps to NM_182961.2 Q7058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr6:152651470 G>A maps to NM_182961.2 H4783H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr6:152652901 C>T maps to NM_182961.2 L4306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr6:152686042 G>A maps to NM_182961.2 Q3362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr6:152527334 C>A maps to NM_182961.2 E7663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:152737831 G>A maps to NM_182961.2 Q1914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr6:152651704 G>A maps to NM_182961.2 A4705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr6:152702359 C>T maps to NM_182961.2 W2930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr6:152555859 T>C maps to NM_182961.2 Q6824Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr6:152510473 G>C maps to NM_182961.2 L7738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr6:152737523 C>T maps to NM_182961.2 Q2016Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr6:152832190 G>T maps to NM_182961.2 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:152555040 C>A maps to NM_182961.2 G6863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T4-01A-11D-A391-08 chr6:152738144 G>A maps to NM_182961.2 H1809H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:152779953 C>A maps to NM_182961.2 E836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr6:152804294 C>G maps to NM_182961.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr14:64518409 G>A maps to NM_182914.2 K2593K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr14:64519340 G>T maps to NM_182914.2 E2904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr14:64519345 G>T maps to NM_182914.2 L2905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr14:64444627 G>C maps to NM_182914.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr14:64522741 C>T maps to NM_182914.2 L3275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr14:64586260 G>A maps to NM_182914.2 L4319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:64457210 C>G maps to NM_182914.2 S799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr14:64520008 T>C maps to NM_182914.2 N3126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr14:64625482 G>A maps to NM_182914.2 E5311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr14:64467417 C>T maps to NM_182914.2 Q1207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr14:64497984 C>G maps to NM_182914.2 G2377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr14:64653140 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr14:64457779 C>T maps to NM_182914.2 Q865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr14:64568721 G>T maps to NM_182914.2 E4152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:64473811 G>A maps to NM_182914.2 E1483E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:64678778 C>G maps to NM_182914.2 S6275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr14:64453208 C>T maps to NM_182914.2 F729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr14:64537451 C>T maps to NM_182914.2 L3507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr14:64634012 C>T maps to NM_182914.2 L5556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr14:64421571 G>C maps to NM_182914.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr14:64532289 G>A maps to NM_182914.2 L3451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr14:64497936 C>T maps to NM_182914.2 L2361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:33400505 G>A maps to NM_006772.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr6:33391252 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr6:33411121 C>T maps to NM_006772.2 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr6:33405755 C>T maps to NM_006772.2 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:33408986 G>T maps to NM_006772.2 E651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr6:33409084 C>T maps to NM_006772.2 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr6:33399936 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr22:39770460 C>T maps to NM_004711.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:76167699 C>T maps to NM_004710.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:76167088 C>T maps to NM_004710.3 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:76166980 C>T maps to NM_004710.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr16:2042985 C>T maps to NM_004209.5 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr19:48878885 C>G maps to NM_012451.3 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr21:34003937 T>C maps to NM_003895.3 Q1402Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr21:34011220 C>T maps to NM_003895.3 P1343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:34045775 G>A maps to NM_003895.3 R573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr21:34072266 C>G maps to NM_003895.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr21:34038864 G>C maps to NM_003895.3 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr21:34004019 G>C maps to NM_003895.3 S1375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr21:34004011 G>A maps to NM_003895.3 Q1378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr6:158516771 A>G maps to NM_003898.3 P1289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:158502269 G>A maps to NM_003898.3 P899P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr6:158504507 G>A maps to NM_003898.3 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr6:158495658 C>T maps to NM_003898.3 F727F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr6:158495691 C>G maps to NM_003898.3 V738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr6:158492756 C>T maps to NM_003898.3 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr14:70839755 G>A maps to NM_018373.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:99672777 C>T maps to ENST00000336292 R1404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr5:150028205 C>T maps to NM_001166209.1 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr5:150028076 C>T maps to NM_001166209.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr5:150028544 C>T maps to NM_001166209.1 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:119947995 G>T maps to NM_133477.2 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr4:119952332 C>T maps to NM_133477.2 T801T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr4:119944685 C>T maps to NM_133477.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr4:119951528 G>A maps to NM_133477.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr4:119951591 C>T maps to NM_133477.2 Y554Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr10:75406721 C>T maps to NM_001114133.1 Q896Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr17:35913379 G>A maps to NM_007247.4 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr17:35913424 G>A maps to NM_007247.4 F800F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr17:35945510 G>C maps to NM_007247.4 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr17:35921618 T>C maps to NM_007247.4 K518K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:35914034 G>C maps to NM_007247.4 S597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:49050798 C>T did not map to a codon.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr23:49050782 C>T did not map to a codon.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr23:49047989 G>T did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:105752609 G>C maps to NM_006754.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:105752621 G>C maps to NM_006754.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr7:105752636 G>A maps to NM_006754.2 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr20:43994260 C>T maps to NM_033542.3 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:79689916 C>G maps to NM_005639.2 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr12:79611343 C>A maps to NM_005639.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr12:79689943 G>A maps to NM_005639.2 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:79837967 A>C maps to NM_005639.2 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr12:33579311 A>T maps to NM_198992.3 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr12:33538175 C>T maps to NM_198992.3 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:33592423 G>A maps to NM_198992.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:33579127 A>G maps to NM_198992.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr12:33560220 C>A maps to NM_198992.3 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr12:33579078 G>C maps to NM_198992.3 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr1:155850995 T>C maps to NM_152280.4 Y331Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:155851154 C>T maps to NM_152280.4 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:155837927 C>T maps to NM_152280.4 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:155851190 G>A maps to NM_152280.4 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr1:155851079 C>T maps to NM_152280.4 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr11:66812098 C>T maps to NM_001177880.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr1:210273592 G>A maps to NM_001146261.1 Q362Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr1:210334176 T>C maps to NM_001146261.1 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:210194441 G>A maps to NM_001146261.1 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:210334290 C>G maps to NM_001146261.1 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:210187103 C>G maps to NM_001146261.1 S108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:210273415 A>G maps to NM_001146261.1 E303E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr10:46962074 G>C maps to NM_031912.3 Y387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr10:46967614 C>T maps to NM_031912.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr10:46963915 G>A maps to NM_031912.3 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr10:46967427 G>A maps to NM_031912.3 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr10:46967520 T>A maps to NM_031912.3 K186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr14:62463083 C>G maps to NM_031914.2 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr14:62547649 C>T maps to NM_031914.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr14:62547862 C>T maps to NM_031914.2 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr14:62550987 T>C maps to NM_031914.2 H503H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr16:19236068 C>T maps to NM_016524.2 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr16:19195315 C>T maps to NM_016524.2 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr16:19278220 G>A maps to NM_016524.2 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:202571538 C>T maps to NM_177402.4 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:202569524 C>T maps to NM_177402.4 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:51140566 C>T maps to NM_001160329.1 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:51128753 C>T maps to NM_001160329.1 K490K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr19:51133271 C>T maps to NM_001160329.1 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr18:40850419 G>A maps to NM_020783.3 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr18:40854177 C>T maps to NM_020783.3 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr18:40853973 C>T maps to NM_020783.3 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:55689629 C>T maps to NM_003180.2 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr19:55690385 C>A maps to NM_003180.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr19:55690343 G>T maps to NM_003180.2 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:55685914 G>A maps to NM_003180.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr1:114680319 G>A maps to ENST00000369545 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:114640499 C>G did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:114640369 C>T maps to ENST00000369545 E498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:1856334 G>A maps to NM_138567.3 K14K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr1:27679977 C>T maps to NM_001193308.1 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr1:27676942 G>A maps to NM_001193308.1 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:27680315 C>G maps to NM_001193308.1 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr11:85420379 G>C maps to ENST00000359152 S1511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr11:85445188 G>A maps to NM_001162953.1 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:85406270 G>T maps to ENST00000359152 L1770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:85411561 G>A maps to ENST00000359152 V1629V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr11:85435075 G>A maps to ENST00000359152 S1332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr11:85445165 T>C maps to NM_001162953.1 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:159173047 C>T maps to ENST00000297239 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr23:99934316 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr23:99931126 T>C did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr23:99955914 G>A did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr23:37955434 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:37935922 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr23:37948732 G>A did not map to a codon.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr23:37913567 C>G did not map to a codon.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr23:37969646 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:37965931 C>G did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:64895934 C>T maps to NM_172230.2 E591E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr11:64900684 C>T maps to NM_172230.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr11:64900693 G>C maps to NM_172230.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr6:166571979 C>A maps to NM_003181.2 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr6:166571940 G>C maps to NM_003181.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr6:166578114 G>A maps to NM_003181.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr6:132966335 G>T maps to NM_138327.1 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr6:132967086 G>C maps to NM_138327.1 S19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:132967037 C>T maps to NM_138327.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr6:132938690 G>A maps to NM_001033080.1 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr6:132909812 C>G maps to NM_003967.2 *338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:132910507 G>C maps to NM_003967.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr6:132910578 G>A maps to NM_003967.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr6:132891942 C>A maps to NM_175067.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr6:132892023 A>G maps to NM_175067.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr6:132860330 T>A maps to NM_175057.3 Y301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr22:39812836 C>T maps to NM_006116.2 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr6:149700619 G>C maps to NM_015093.4 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr6:149700404 C>T maps to NM_015093.4 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr23:30852245 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr23:30872613 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:30873149 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr23:30870917 T>A did not map to a codon.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr23:30872792 G>C did not map to a codon.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr23:30873253 T>C did not map to a codon.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr23:30873149 C>G did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr23:30873456 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr23:30872937 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:97362007 G>A maps to NM_003182.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr8:38677715 C>G maps to ENST00000379931 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr8:38677878 C>T maps to ENST00000379931 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr8:38699937 G>A maps to ENST00000379931 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr10:123843280 C>T maps to NM_206862.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr10:123845110 G>A maps to NM_206862.2 K1032K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:123844549 C>G maps to NM_206862.2 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:123844345 G>A maps to NM_206862.2 G777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr10:123845773 G>A maps to NM_206862.2 V1253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:123844285 G>A maps to NM_206862.2 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr10:123845773 G>A maps to NM_206862.2 V1253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr10:123842815 G>A maps to NM_206862.2 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:124008178 C>G maps to NM_206862.2 S2805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr10:124008641 G>A maps to NM_206862.2 L2877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr10:123846946 T>C maps to NM_206862.2 P1644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr10:123846907 G>C maps to NM_206862.2 T1631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr10:123846220 C>T maps to NM_206862.2 L1402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr10:123842414 C>T maps to NM_206862.2 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:123845749 G>A maps to NM_206862.2 Q1245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr4:1746694 G>T maps to NM_006342.1 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:1746258 G>A maps to NM_006342.1 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:1739042 A>G maps to NM_006342.1 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr4:1730406 C>T maps to NM_006342.1 C426C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr17:61685196 G>A maps to NM_016360.3 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr17:61678639 C>T maps to NM_016360.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr17:61678657 G>A maps to NM_016360.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr4:104510982 T>C maps to NM_001059.2 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr4:104640577 G>A maps to NM_001059.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr4:104640409 G>A maps to NM_001059.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:104579412 G>T maps to NM_001059.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr4:104579485 C>T maps to NM_001059.2 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:59042363 G>A maps to NM_002353.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:59042552 C>G maps to NM_002353.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:166845421 C>A maps to NM_053053.3 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:35800674 C>T maps to NM_001166105.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:7056369 C>G maps to NM_152293.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr23:70643043 C>A did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr23:70608123 G>A did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr23:70601651 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr23:70621445 A>G did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:70621379 G>C did not map to a codon.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr23:70643023 G>A did not map to a codon.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr23:70627846 C>G did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr23:70598721 G>A did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:70683803 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr23:70627985 A>G did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:70597011 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:70679431 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr23:70621438 A>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:70607184 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:6632653 C>T maps to NM_006284.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:34846497 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr6:34848063 A>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:109617650 C>A maps to NM_005645.3 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:109608819 C>T maps to NM_005645.3 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:34149812 G>T maps to NM_139215.1 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:34171326 C>T maps to NM_139215.1 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:222743963 G>A maps to NM_005681.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr2:10053351 A>G maps to NM_005680.2 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr2:10016134 C>G maps to NM_005680.2 S232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr16:84212581 G>A maps to NM_005679.2 Q859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:84215614 C>T maps to NM_005679.2 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr16:84215838 G>C maps to NM_005679.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr16:84213621 G>A maps to NM_005679.2 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr11:93470345 C>T maps to NM_024116.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr11:93471530 G>T maps to NM_024116.3 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr9:32633771 G>A maps to NM_153809.2 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr9:32634549 G>C maps to NM_153809.2 S343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr9:32632466 T>C maps to NM_153809.2 K1037K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAME-01A-12D-A42E-08 chr9:32630357 T>C maps to NM_153809.2 G1740G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr9:32635515 G>C maps to NM_153809.2 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr8:120843963 G>A maps to NM_003184.3 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr8:120756537 C>T maps to NM_003184.3 P1068P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr8:120809279 G>A maps to NM_003184.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr8:120790294 T>C maps to NM_003184.3 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr8:120844795 C>T maps to NM_003184.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr10:8006852 C>T maps to NM_031923.2 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr20:60581775 G>A maps to NM_003185.3 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr20:60578916 C>T maps to NM_003185.3 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr20:60584122 G>A maps to NM_003185.3 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr18:23866324 G>A maps to ENST00000418698 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr18:23915182 G>A maps to ENST00000418698 Q773Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr18:23873439 C>T maps to ENST00000418698 Q598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr18:23845164 G>A maps to ENST00000418698 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr18:23873397 C>T maps to ENST00000418698 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr10:105128036 A>G maps to NM_006951.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr10:105128237 G>T maps to NM_006951.3 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr10:105128279 C>A maps to NM_006951.3 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:229730259 G>A maps to NM_014409.3 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr1:229738100 C>T maps to NM_014409.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:99710523 C>T maps to ENST00000472509 Q214Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr7:99709784 G>C maps to ENST00000472509 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr7:99704882 G>A maps to ENST00000472509 Q731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:62553844 C>T maps to NM_006473.2 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr11:62554254 G>A maps to NM_006473.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr11:62554062 G>A maps to NM_006473.2 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr5:140698973 G>C maps to NM_005642.2 S213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:100537422 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr23:100532626 T>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:100533059 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:100542500 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr23:100532613 T>C did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr23:100524222 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:100531441 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr23:100542467 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr6:42019183 G>A maps to NM_138572.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr5:68660802 G>A maps to NM_001015892.1 D254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr5:68651778 C>T maps to NM_016283.4 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr23:77393571 C>T did not map to a codon.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr6:159457209 C>T maps to NM_054114.3 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr6:159457743 C>T maps to NM_054114.3 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:117073782 C>T maps to NM_003186.3 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr11:117074162 C>T maps to NM_003186.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr1:47691455 G>A maps to ENST00000371883 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:763391 C>T maps to NM_006755.1 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr11:764429 G>A maps to NM_006755.1 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr11:763867 C>T maps to NM_006755.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:160035371 C>T maps to NM_033394.2 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5U8-01A-11D-A289-08 chr2:160006933 C>T maps to NM_033394.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:160075866 C>G maps to NM_033394.2 S1166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr2:160043507 C>G maps to NM_033394.2 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr2:160035086 A>G maps to NM_033394.2 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:160027153 G>T maps to NM_033394.2 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr2:160075858 C>T maps to NM_033394.2 F1163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr2:160086682 A>G maps to NM_033394.2 L1582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr2:160086611 C>T maps to NM_033394.2 Q1559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr2:160086760 C>T maps to NM_033394.2 R1608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr2:160043417 C>G maps to NM_033394.2 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr17:61417590 G>T maps to ENST00000389520 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr17:61432166 C>T maps to ENST00000389520 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr17:61271409 C>A maps to ENST00000389520 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:61488929 G>A maps to ENST00000389520 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:61497893 C>T maps to ENST00000389520 S1527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr17:61432634 C>G maps to ENST00000389520 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr17:61498586 G>A maps to ENST00000389520 S1758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr2:162092022 G>A maps to NM_004180.2 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr17:27778619 C>T maps to NM_020791.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:27822624 C>G maps to NM_020791.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr16:30002498 G>A maps to NM_004783.2 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:29993015 G>A maps to NM_016151.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:29994161 G>A maps to NM_016151.2 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr16:29998445 C>G maps to NM_016151.2 L951L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr16:30002178 C>T maps to NM_004783.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr12:118671554 C>T maps to NM_016281.3 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:118637038 C>T maps to NM_016281.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr6:32815406 G>A maps to NM_000593.5 Q656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr6:32821185 G>A maps to NM_000593.5 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:33281009 G>A maps to NM_172208.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:16175862 C>G maps to NM_153365.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr1:234541778 G>A maps to NM_005646.3 R1287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr1:234561433 G>A maps to NM_005646.3 I1143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr1:234553934 G>A maps to NM_005646.3 F1200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr1:234593466 G>A maps to NM_005646.3 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr1:234565224 G>A maps to NM_005646.3 L936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr12:53899527 C>T maps to NM_134323.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr12:53899930 G>A maps to NM_134323.1 *367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr12:53895840 C>T maps to NM_134323.1 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:53899599 G>A maps to NM_134323.1 E303E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:11080560 C>T maps to NM_007375.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:11078794 G>A maps to NM_007375.3 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:11076933 C>A maps to NM_007375.3 S91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr5:33459810 G>A maps to ENST00000455217 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:33467053 C>T maps to ENST00000455217 R696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:150477197 C>T maps to NM_025150.3 C603C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr1:150463905 G>A maps to NM_025150.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr15:102242447 G>A maps to NM_152334.2 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:6634782 G>A maps to NM_138697.3 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:6639094 C>A maps to NM_138697.3 I659I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:6639058 C>T maps to NM_138697.3 S647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr1:6639331 C>T maps to NM_138697.3 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr1:6639337 C>T maps to NM_138697.3 I740I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:6639028 C>G maps to NM_138697.3 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr1:6639580 C>A maps to NM_138697.3 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:19186031 G>C maps to NM_152232.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr1:19180733 G>A maps to NM_152232.2 C410C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:19166503 A>G maps to NM_152232.2 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr1:19166689 G>A maps to NM_152232.2 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:19166383 G>A maps to NM_152232.2 F743F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr1:1267822 G>A maps to NM_152228.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:1267275 C>T maps to NM_152228.1 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr1:1268917 G>T maps to NM_152228.1 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr1:1268323 G>A maps to NM_152228.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr1:1269300 G>A maps to NM_152228.1 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:1267924 G>A maps to NM_152228.1 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:1268135 C>T maps to NM_152228.1 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:1266781 G>A maps to NM_152228.1 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr5:9629538 C>T maps to NM_019599.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:11061114 C>G maps to NM_023920.2 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr12:11090853 C>T maps to NM_023922.1 *318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:11091005 C>T maps to NM_023922.1 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr7:122635436 G>A maps to NM_016945.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr7:122635517 G>A maps to NM_016945.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:11175080 T>A maps to NM_176888.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr12:11174600 C>T maps to NM_176888.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr12:11149554 G>C maps to NM_176889.2 S307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr12:11150168 G>A maps to NM_176889.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr12:11149898 C>G maps to NM_176889.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr7:141464275 C>G maps to NM_016943.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr7:141464314 C>T maps to NM_016943.2 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:11183790 G>C maps to NM_176885.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr12:11183610 G>C maps to NM_176885.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr12:11183628 G>T maps to NM_176885.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr12:11183913 G>A maps to NM_176885.2 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr12:11183151 G>A maps to NM_176885.2 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr7:142880648 C>A maps to NM_176881.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr7:142881176 C>T maps to NM_176881.2 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr7:142880768 C>G maps to NM_176881.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr7:142881080 C>T maps to NM_176881.2 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr7:142919935 C>T maps to NM_176882.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr7:143175354 G>T maps to NM_176883.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:11339183 G>A maps to NM_181429.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:11244750 G>A maps to ENST00000422992 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:11214170 G>T maps to ENST00000422992 Y241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr12:11214587 G>A maps to NM_176887.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr12:11214859 G>A maps to NM_176887.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr7:141490475 G>A maps to NM_018980.2 K105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr7:141490166 G>A maps to NM_018980.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr12:11139048 C>T maps to NM_176890.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr12:11139384 G>C maps to NM_176890.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:143141090 C>T maps to NM_177437.1 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:10959333 C>T maps to NM_023918.1 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr12:10958928 G>C maps to NM_023918.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:10959254 G>A maps to NM_023918.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr12:10962173 C>T maps to NM_023917.2 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:13415693 G>A maps to NM_017714.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr20:13514764 G>A maps to NM_017714.2 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:71610276 G>C maps to NM_000353.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr16:71604296 G>A maps to NM_000353.2 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:10290961 C>G maps to NM_014760.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr7:27797747 C>T maps to ENST00000409980 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr7:27797660 T>C maps to ENST00000409980 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr7:27856052 C>G maps to ENST00000409980 S641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr23:153648554 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr23:153648390 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr23:153649010 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr23:153640474 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr23:153640482 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr23:153647889 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:153640429 G>T did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr4:38126706 G>A maps to NM_015173.2 T1029T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr4:38022295 C>T maps to NM_015173.2 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr4:37903994 C>T maps to NM_015173.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr4:38134764 C>T maps to NM_015173.2 Q1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr4:38016206 C>T maps to NM_015173.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr4:38016320 C>G maps to NM_015173.2 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr4:38051358 C>T maps to NM_015173.2 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr4:38016440 G>A maps to NM_015173.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr4:38138895 G>A maps to NM_015173.2 R1149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr4:38117391 T>C maps to NM_015173.2 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr4:38020000 C>T maps to NM_015173.2 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr4:38091733 C>G maps to NM_015173.2 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr22:30722864 C>T maps to ENST00000403477 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr16:30376494 G>A maps to NM_015527.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr16:30376854 G>A maps to NM_015527.3 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:67172955 G>A maps to NM_198517.2 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAME-01A-12D-A42E-08 chr10:96269872 C>T maps to NM_015188.1 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr9:131553893 G>C maps to NM_018201.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:131565698 C>T maps to NM_018201.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:131566274 C>T maps to NM_018201.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:131566385 C>G maps to NM_018201.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:131568172 C>T maps to NM_018201.3 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:131568241 C>G maps to NM_018201.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr4:6925316 G>A maps to NM_001113361.1 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr4:7016173 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:6969150 G>A maps to NM_001113361.1 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr4:7032082 G>A maps to NM_001113361.1 R682R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr12:72312285 C>T maps to NM_022771.4 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr12:72288485 T>C maps to NM_022771.4 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr17:77925391 C>A maps to NM_019020.2 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:77924272 G>A maps to NM_019020.2 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr17:77984048 G>T maps to NM_019020.2 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr17:77926583 G>A maps to NM_019020.2 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:50387618 C>T maps to NM_024682.2 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr4:26675452 C>T maps to NM_018317.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr9:100963835 G>A maps to NM_018421.3 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr20:422525 C>A maps to ENST00000246077 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:420954 G>A maps to ENST00000246077 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr20:422260 C>T maps to ENST00000246077 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr22:47307989 C>T maps to NM_014346.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr6:37280748 C>T maps to NM_017772.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr3:100029350 C>T maps to ENST00000394144 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:99979885 G>T maps to ENST00000394144 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr3:100013993 C>T maps to ENST00000394144 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr3:100009529 C>A maps to ENST00000394144 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr16:2546211 C>T maps to ENST00000434757 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr16:2546964 C>T maps to ENST00000434757 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:48418784 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:48418555 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:48419300 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr23:48417711 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr15:78346478 C>T maps to NM_144572.1 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:78316700 G>A maps to NM_144572.1 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:34499226 G>A maps to NM_001001417.5 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr13:75898392 T>A maps to ENST00000431480 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr13:75936293 G>A maps to ENST00000431480 C316C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr13:75933987 G>A maps to ENST00000431480 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:75900456 G>A maps to ENST00000431480 R637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr13:75861110 C>T maps to ENST00000431480 L1239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr13:76055516 G>A maps to ENST00000431480 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr13:75873563 G>A maps to ENST00000431480 L1021L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr13:75900526 T>A maps to ENST00000431480 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr13:76055672 C>T maps to ENST00000431480 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr3:17418075 G>C maps to NM_001134381.1 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr3:17208348 G>A maps to NM_001134381.1 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:13307929 C>T maps to NM_016495.4 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:101655102 C>T maps to NM_001102426.1 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr2:101627947 G>C maps to NM_001102426.1 S946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr2:101656804 G>A maps to NM_001102426.1 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr2:101670702 G>A maps to NM_001102426.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr2:101624339 G>A maps to NM_001102426.1 L1122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr23:106083997 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr23:106082550 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr23:106069396 T>C did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr23:106046198 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr23:106069464 G>C did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr23:106110052 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:106066676 C>G did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr23:106091463 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:106065308 G>C did not map to a codon.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr23:106070523 G>C did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr23:106117132 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:106062001 T>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr23:106093527 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr23:106109142 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:106046147 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:106065248 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:106116800 C>G did not map to a codon.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr4:141543600 G>A maps to NM_015130.2 I1183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr4:141543699 C>T maps to NM_015130.2 L1150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FM-01A-11D-A38G-08 chr4:141590904 G>A maps to NM_015130.2 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr4:141578844 T>C maps to NM_015130.2 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr4:141555213 G>C maps to NM_015130.2 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:141545486 C>T maps to NM_015130.2 V985V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr5:179318450 G>A maps to NM_198868.2 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:179321392 C>A maps to NM_198868.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr5:179306732 G>A maps to NM_198868.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr5:179302098 G>A maps to NM_198868.2 I663I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr5:179290666 G>A maps to NM_198868.2 G1178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr5:179290570 C>T maps to NM_198868.2 E1210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr5:179290558 C>T maps to NM_198868.2 V1214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr19:36606494 G>A maps to NM_001281.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:42713400 G>A maps to NM_003192.2 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr6:42713667 C>T maps to NM_003192.2 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:80887348 G>T maps to NM_005993.4 V988V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:80899326 C>T maps to NM_005993.4 L1178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr17:80858592 C>T maps to NM_005993.4 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr17:80763784 C>T maps to NM_005993.4 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:80828221 C>T maps to NM_005993.4 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr17:80847545 C>T maps to NM_005993.4 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr17:80758803 G>A maps to NM_005993.4 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr17:80885816 G>C maps to NM_005993.4 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr17:80890566 C>T maps to NM_005993.4 H1049H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:235577753 G>A maps to NM_003193.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:235611709 C>G maps to NM_003193.3 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr1:235602229 C>G maps to NM_003193.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:120918360 C>T maps to NM_152715.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:45773486 C>T maps to NM_014726.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr17:45774087 C>T maps to NM_014726.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:45787907 C>A maps to NM_014726.2 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr23:9622317 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr23:9622273 C>G did not map to a codon.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr23:9659695 G>T did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:9682997 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr23:9656164 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr23:9684282 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr3:176750884 G>A maps to NM_024665.4 D430D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr3:176771706 C>T did not map to a codon.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr3:176765186 T>C did not map to a codon.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr24:6911148 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr24:6954348 G>A did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr24:6942599 G>A did not map to a codon.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr7:72987256 G>A maps to NM_012453.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr7:72988742 G>A maps to NM_012453.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr7:72985535 G>A maps to NM_012453.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:2028583 C>G maps to NM_006453.2 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:2026925 C>T maps to NM_006453.2 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr6:170866125 G>A maps to NM_003194.4 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr6:170871045 A>G maps to NM_003194.4 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr6:170871039 A>G maps to NM_003194.4 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr6:170871045 A>G maps to NM_003194.4 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr2:162273469 C>T maps to NM_006593.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:162273100 G>A maps to NM_006593.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr2:162273337 C>T maps to NM_006593.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr22:19754182 C>T maps to NM_080647.1 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:67402489 C>T maps to NM_005995.4 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr11:67401658 C>T did not map to a codon.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr11:67402341 G>A maps to NM_005995.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr1:119427659 G>A maps to ENST00000369429 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:119456780 G>A maps to ENST00000369429 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr1:119427356 A>T maps to ENST00000369429 *603K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr6:85446792 G>A maps to NM_001080508.1 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr6:85473827 C>T maps to NM_001080508.1 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:168278088 C>G maps to NM_005149.2 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:168277997 C>G maps to NM_005149.2 S312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr1:168260523 C>T maps to NM_005149.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:59479062 C>T maps to NM_005994.3 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr23:79282268 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:79277856 C>T did not map to a codon.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr23:79278580 C>T did not map to a codon.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr23:79283539 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:79283515 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:115114190 T>C maps to NM_016569.3 E342E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr17:59560438 G>A maps to ENST00000393853 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr17:59560723 C>T maps to ENST00000393853 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr17:59557512 C>G maps to ENST00000393853 S285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr12:114836394 G>A maps to NM_000192.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr12:114823366 C>T maps to NM_000192.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr12:114793705 G>A maps to NM_000192.3 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr12:114823312 G>A maps to NM_000192.3 D241D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr7:139636072 G>A maps to NM_001166253.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:139661803 C>T maps to NM_001166253.1 D349D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr7:139717521 C>T maps to NM_001166253.1 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:139662001 G>A maps to NM_001166253.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr14:92264743 C>G did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:92268666 G>A maps to NM_001128596.1 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:37822004 G>A maps to NM_003673.3 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr20:62701682 G>C maps to NM_003195.4 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:102885009 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr23:101381894 A>C did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:101382354 A>G did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr23:102864367 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:102529332 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:102529346 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr23:102529117 T>A did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr23:102508662 A>G did not map to a codon.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr23:102508573 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:102508733 G>A did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr23:13681433 G>C did not map to a codon.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr1:24078327 C>T maps to NM_003198.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:24078044 C>G maps to NM_003198.2 S343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr18:44559493 C>T maps to NM_016427.2 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr18:44560636 C>T maps to NM_016427.2 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr18:44560877 G>T maps to NM_016427.2 S253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr18:44560256 G>C maps to NM_016427.2 S460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr18:44555256 C>T maps to NM_145653.3 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr18:44555114 G>A maps to NM_145653.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr18:44555294 C>A maps to NM_145653.3 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:44554604 G>A maps to NM_145653.3 R537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr18:44555035 C>T maps to NM_145653.3 W393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr18:44555157 G>C maps to NM_145653.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr18:44555307 C>T maps to NM_145653.3 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr18:44549208 C>A maps to NM_145653.3 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr18:44555022 G>A maps to NM_145653.3 C397C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr5:145890060 A>G maps to NM_006706.3 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr5:145883547 C>T maps to NM_006706.3 F903F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr10:132891522 G>A maps to NM_174937.3 Q555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:31127451 G>A maps to NM_007109.2 W69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:31127452 G>A maps to NM_007109.2 W69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr22:42564659 C>T maps to NM_005650.1 *1961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr22:42606217 C>A maps to NM_005650.1 S1698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr22:42609616 C>T maps to NM_005650.1 Q565Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr22:42610591 G>A maps to NM_005650.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:42606364 G>A maps to NM_005650.1 I1649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr22:42609222 C>A maps to NM_005650.1 E697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr22:42606328 C>T maps to NM_005650.1 V1661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr22:42608763 G>A maps to NM_005650.1 Q850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr22:42609135 G>A maps to NM_005650.1 Q726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr6:134210811 C>T maps to NM_003206.3 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:134210741 G>A maps to NM_003206.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr2:27373016 G>A maps to NM_175769.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr2:27373034 C>A maps to NM_175769.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:27375554 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:89940209 C>T maps to NM_014972.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr16:89958627 C>T maps to NM_014972.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr16:89973697 G>C maps to NM_014972.2 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:89962446 C>T maps to NM_014972.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr16:89965048 C>A maps to NM_014972.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr16:89965216 C>T maps to NM_014972.2 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr16:89977037 C>T maps to NM_014972.2 F613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:1615434 C>T maps to NM_003200.2 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr18:52946873 G>C maps to ENST00000398339 S290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr18:53254338 G>A maps to ENST00000398339 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr18:53254299 C>G maps to ENST00000398339 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr18:53070730 G>T maps to ENST00000398339 S210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr5:133478562 C>T maps to ENST00000395029 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr2:85533376 G>A maps to NM_031283.2 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr10:114900992 G>T maps to NM_030756.4 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr10:114711347 C>G maps to NM_030756.4 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr10:114925397 G>A maps to NM_030756.4 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr10:114710568 G>A maps to NM_030756.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr10:114919694 G>A maps to NM_030756.4 K439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr20:61485439 C>T maps to NM_006602.2 K436K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:152083886 C>T maps to NM_007113.2 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:152083963 G>A maps to NM_007113.2 Q577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:152083291 C>A maps to NM_007113.2 E801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:152081564 G>A maps to NM_007113.2 F1376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:152084108 G>A maps to NM_007113.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr1:152081423 C>T maps to NM_007113.2 L1423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:152082230 C>T maps to NM_007113.2 L1154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr1:152080025 C>T maps to NM_007113.2 Q1889Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr1:152080592 G>A maps to NM_007113.2 L1700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:152082860 C>G maps to NM_007113.2 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:152084600 C>G maps to NM_007113.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr1:152058909 G>T maps to NM_001008536.1 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:152060607 G>C maps to NM_001008536.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:152058702 G>A maps to NM_001008536.1 N485N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:152059842 C>T maps to NM_001008536.1 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:152057442 T>C maps to NM_001008536.1 *905W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:152060592 G>C maps to NM_001008536.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:110341853 G>T maps to NM_032300.4 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr12:110345341 C>T maps to NM_032300.4 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:110353292 C>G maps to NM_032300.4 S469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr11:67817158 G>C maps to NM_006019.3 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr11:59623429 A>G maps to NM_001062.3 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr11:59622250 G>C maps to NM_001062.3 S332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr22:31011459 G>A maps to NM_000355.3 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:31019014 C>T maps to NM_000355.3 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr5:149758895 G>A maps to ENST00000451292 Q861Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:149754545 C>T maps to ENST00000451292 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr5:149771566 C>A maps to ENST00000451292 T1152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr5:149754599 A>T maps to ENST00000451292 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr6:160210476 G>A maps to NM_030752.2 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr6:160205737 G>A maps to NM_030752.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr6:167590517 C>T maps to NM_001145121.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr6:167595346 G>A maps to NM_001145121.1 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr6:35088707 C>T maps to NM_001093728.1 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr6:35088698 G>C maps to NM_001093728.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr12:106712242 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr12:106712229 A>G maps to NM_152772.1 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:49449865 G>T maps to NM_022171.2 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr3:49452276 C>G maps to NM_022171.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr6:44254162 C>T maps to NM_182539.3 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr6:44254252 C>T maps to NM_182539.3 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr12:111085636 C>T maps to NM_001082538.2 F573F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr12:111072479 C>T maps to NM_001082538.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:111052136 G>A maps to NM_001082538.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr12:124171450 C>G maps to NM_024809.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr12:124156666 G>A maps to NM_024809.3 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:124179518 G>A maps to NM_024809.3 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:46621500 C>T maps to NM_003212.3 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr4:156828901 C>T maps to NM_005651.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr4:156828925 G>A maps to NM_005651.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr14:90455253 G>A maps to NM_018319.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr14:90442141 G>A maps to NM_018319.3 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr14:90437608 C>T maps to NM_018319.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:90429871 C>G maps to NM_018319.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr10:115947865 C>T maps to NM_198795.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr10:115970724 A>G maps to NM_198795.1 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:115978318 C>T maps to NM_198795.1 Q824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr10:115964593 C>T maps to NM_198795.1 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr10:115970460 C>T maps to NM_198795.1 H502H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:154493837 A>G maps to NM_001098475.1 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr13:61057915 C>G maps to NM_001146070.1 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr13:61102942 T>A maps to NM_001146070.1 Y528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:179600038 G>A maps to ENST00000444136 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr1:179660076 G>A maps to ENST00000444136 *1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:46658619 G>T maps to NM_001010870.2 E919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:46661435 G>A maps to NM_001010870.2 Q1857Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr6:46657988 G>A maps to NM_001010870.2 Q708Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:46660715 C>G maps to NM_001010870.2 L1617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:46661398 C>G maps to NM_001010870.2 S1845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:46656863 G>A maps to NM_001010870.2 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr6:46663620 C>G maps to NM_001010870.2 S2037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr9:100234692 C>G maps to NM_014290.2 Y620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr9:100249559 C>T maps to NM_014290.2 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:100234722 C>T maps to NM_014290.2 I630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr9:100222555 C>T maps to NM_014290.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr9:100245327 G>A maps to NM_014290.2 S870S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr9:100258130 C>G maps to NM_014290.2 S1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr9:100245528 G>A maps to NM_014290.2 K937K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr9:100190851 T>A maps to NM_014290.2 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr14:104472827 C>T maps to NM_153046.2 Q606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr14:104492031 C>T maps to NM_153046.2 V950V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr14:104490992 C>T maps to NM_153046.2 L898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr14:104471726 C>T maps to NM_153046.2 I566I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr14:104474763 G>A maps to NM_153046.2 W689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:151751266 G>A maps to NM_001083965.1 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:151752450 G>A maps to NM_001083965.1 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:151748296 T>G maps to NM_001083965.1 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr11:12901331 T>A maps to NM_021961.5 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:12958690 C>G maps to NM_021961.5 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr19:49844634 G>C maps to NM_003598.1 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr19:49854573 T>A maps to NM_003598.1 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:49863218 G>T maps to NM_003598.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr6:35444183 T>C maps to ENST00000357281 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:35443425 G>A maps to ENST00000357281 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr6:35443740 G>T maps to ENST00000357281 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr12:3104054 C>A maps to NM_003213.3 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr12:3104096 C>A maps to NM_003213.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr12:3104132 C>T maps to NM_003213.3 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr4:48170605 C>T maps to NM_003215.2 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr4:48158748 C>T maps to NM_003215.2 W247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr4:48140930 G>A maps to NM_003215.2 V548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr4:48169814 C>T maps to NM_003215.2 W217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr7:97867838 G>A maps to ENST00000379795 N339N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr7:97862207 G>A maps to ENST00000379795 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr7:97862829 C>G maps to ENST00000379795 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr7:97873930 C>T maps to ENST00000379795 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr7:97860325 G>A maps to ENST00000379795 S744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr14:102904405 C>A maps to NM_014844.3 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr14:102904528 A>G maps to NM_014844.3 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr14:102916060 C>T maps to NM_014844.3 P1057P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr14:102873780 C>G maps to NM_014844.3 S109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:102906782 C>G maps to NM_014844.3 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr14:102931586 C>T maps to NM_014844.3 L1250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr14:102904539 C>A maps to NM_014844.3 S859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:14640522 G>A maps to NM_138501.4 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:14673365 G>A maps to ENST00000436007 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr4:65274919 T>C maps to NM_001010874.4 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr4:65188508 G>A maps to NM_001010874.4 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr4:65194274 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:65147236 G>A maps to NM_001010874.4 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr4:65146798 T>C maps to NM_001010874.4 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:65194230 A>G maps to NM_001010874.4 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr11:120980086 G>A maps to NM_005422.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr11:121039496 G>C maps to NM_005422.2 T1954T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr11:120998485 C>T maps to NM_005422.2 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:120998962 C>T maps to NM_005422.2 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:121037302 C>T maps to NM_005422.2 I1800I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr11:121028926 G>A maps to NM_005422.2 T1561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr11:120976570 G>A maps to NM_005422.2 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr11:120984326 C>T maps to NM_005422.2 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:114045914 C>T maps to NM_058222.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:182368981 C>T maps to NM_172000.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr1:182369425 G>A maps to NM_172000.3 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr1:182368921 C>G maps to NM_172000.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr1:182368844 G>T maps to NM_172000.3 S259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr22:41791840 C>A maps to ENST00000417325 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr9:27169598 C>T maps to NM_000459.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr9:27202917 T>C maps to NM_000459.3 I670I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr9:27217714 C>T maps to NM_000459.3 I1007I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:6719157 C>T maps to NM_053285.1 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr17:6722591 G>A maps to NM_053285.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr17:6733598 G>A maps to NM_053285.1 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr17:6718585 C>T maps to NM_053285.1 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:36550831 G>A maps to NM_014466.2 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr17:15215635 G>A maps to NM_031898.2 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:15215661 G>A maps to NM_031898.2 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:95537569 C>T maps to NM_144705.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr16:10783857 G>A maps to NM_144674.1 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr16:1551482 C>T maps to NM_016111.3 D448D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr16:1552119 C>T maps to NM_016111.3 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr16:1556997 C>T maps to NM_016111.3 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr16:1547091 C>A maps to NM_016111.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr12:53454001 G>A maps to NM_170754.2 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr14:20850178 C>T maps to NM_007110.4 R1439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:20841486 G>A maps to NM_007110.4 L2252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr14:20876253 G>A maps to NM_007110.4 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr14:20876346 T>A maps to NM_007110.4 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr14:20848087 C>A did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr14:20848599 G>A maps to NM_007110.4 P1599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr14:20845843 G>A maps to NM_007110.4 A1930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr14:20851966 G>A maps to NM_007110.4 L1215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr14:20859210 C>T maps to NM_007110.4 T714T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr14:20852017 G>A maps to NM_007110.4 F1198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr14:20852558 G>A maps to NM_007110.4 L1110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr14:20871926 C>T maps to NM_007110.4 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr14:20852873 T>G did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr16:58010488 T>G maps to NM_199046.2 Y38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr16:69400864 C>T maps to NM_005652.3 K353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:69419339 C>T maps to NM_005652.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr16:75681785 G>T maps to NM_018975.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr5:1293551 G>A maps to NM_198253.2 N483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr5:1294370 G>A maps to NM_198253.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr5:1278890 G>A maps to NM_198253.2 Y717Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr7:115892472 C>T maps to NM_015641.2 Y340Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr12:117513133 G>A maps to ENST00000392545 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr9:35606895 C>T maps to NM_006285.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:45811225 G>A maps to NM_007170.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:45887428 G>A maps to NM_007170.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr1:45810575 G>C maps to NM_007170.2 S551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr10:70411672 C>T maps to NM_030625.2 V1449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr10:70332213 C>G maps to NM_030625.2 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr10:70332552 C>G maps to NM_030625.2 S153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr10:70333654 G>A maps to NM_030625.2 E520E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr10:70333943 C>T maps to NM_030625.2 Q617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:70442601 G>T maps to NM_030625.2 E1642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr10:70405514 C>G maps to NM_030625.2 S1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr10:70406449 C>T maps to NM_030625.2 Q1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr10:70333765 C>T maps to NM_030625.2 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr10:70333543 A>T maps to NM_030625.2 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr4:106156624 C>G maps to ENST00000513237 S530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr4:106155203 G>A maps to ENST00000513237 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr4:106157171 T>G maps to ENST00000513237 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:106156445 G>C maps to ENST00000513237 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr2:74329137 G>A maps to ENST00000409262 G1648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr2:74329092 G>A maps to ENST00000409262 E1633E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr2:74328834 G>T maps to ENST00000409262 S1547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr2:74273925 C>A maps to ENST00000409262 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:103070857 G>A maps to NM_017746.3 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr9:103090141 G>T maps to NM_017746.3 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:43922099 T>C maps to NM_031451.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr23:70099854 C>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:70053442 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr23:70080734 G>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:69749755 C>T did not map to a codon.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr23:69749012 C>A did not map to a codon.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr23:69773217 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:69871317 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr23:104463695 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:104464970 C>G did not map to a codon.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr23:107224540 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr23:107224420 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr23:107224559 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:56676845 G>A maps to ENST00000240361 F626F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr17:56651578 C>A maps to ENST00000240361 E1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:56690859 G>A maps to ENST00000240361 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:56676605 G>C maps to ENST00000240361 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr8:30699657 C>T maps to NM_031271.3 T2292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:30694785 G>T maps to NM_031271.3 S2622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:30702045 G>T maps to NM_031271.3 I1496I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr8:30705623 C>A maps to NM_031271.3 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr17:62254696 G>T maps to NM_018469.3 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr17:62248556 G>C maps to NM_018469.3 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr17:62290908 C>T maps to NM_018469.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr17:62290562 C>A maps to NM_018469.3 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr2:71218972 G>A maps to NM_144582.2 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr3:51733522 G>A maps to NM_015926.4 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr15:56719897 G>A maps to NM_198524.1 K353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr15:56683502 C>G maps to NM_198524.1 S153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr15:56680667 A>G did not map to a codon.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr3:133475705 G>A maps to NM_001063.3 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:133494391 C>T maps to NM_001063.3 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr3:133478067 G>A maps to NM_001063.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:133473510 G>A maps to NM_001063.3 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr3:133467352 C>T maps to NM_001063.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr10:60148580 T>G did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:60145994 G>A maps to NM_003201.1 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr6:10410426 G>A maps to ENST00000379613 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr6:10410337 C>T maps to ENST00000379613 Q94Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr6:10404841 G>A maps to ENST00000379613 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr6:10404772 G>C maps to ENST00000379613 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr6:50803828 G>C maps to ENST00000263046 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:50805696 G>A maps to ENST00000263046 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr6:50791307 C>T maps to ENST00000263046 N99N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr6:50786663 C>G maps to ENST00000263046 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr20:55206427 G>A maps to NM_003222.3 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr20:55212939 G>T maps to NM_003222.3 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr20:55209241 G>A maps to NM_003222.3 E280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr6:50683245 C>T maps to NM_172238.3 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr6:50718974 G>A maps to NM_172238.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:50740450 A>G maps to NM_172238.3 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr6:50696936 G>C maps to NM_172238.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr1:36053973 G>A maps to NM_178548.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:4310138 G>A maps to NM_003223.2 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:4322722 G>A maps to NM_003223.2 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr16:4310207 C>T maps to NM_003223.2 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:246704482 C>T maps to NM_022366.2 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr12:51492567 G>A maps to NM_005653.4 I470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:51500366 G>A maps to NM_005653.4 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr2:122038801 C>A maps to NM_014553.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:122042676 G>A maps to NM_014553.2 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr2:122005741 G>A maps to NM_014553.2 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:141671501 G>C maps to NM_001178139.1 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr3:141671820 T>C maps to NM_001178139.1 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr3:141688983 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr3:141678555 C>T maps to NM_001178139.1 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr23:48896787 C>A did not map to a codon.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr23:48895848 G>A did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr23:48895742 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:48890999 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr23:48895738 A>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr23:48891043 T>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr23:48888995 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr6:41654866 C>T maps to ENST00000343317 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr7:115624333 A>G maps to NM_012252.2 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr21:43783376 G>A maps to NM_003225.2 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr21:43767667 G>A maps to NM_005423.4 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:100432574 C>T maps to NM_001007565.2 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:100432660 C>T maps to NM_001007565.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:100432574 C>T maps to NM_001007565.2 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:100467339 C>T maps to NM_001007565.2 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr3:100463741 C>T maps to NM_001007565.2 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr3:100467056 A>T maps to NM_001007565.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:100467243 C>T maps to NM_001007565.2 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr22:26895342 G>C maps to NM_012143.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5N-01A-11D-A42E-08 chr22:26902779 G>A maps to NM_012143.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr7:93519631 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:54617949 G>A maps to NM_013342.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:100228519 G>C maps to NM_003227.3 S421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr7:100225559 C>G maps to NM_003227.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr7:100225577 G>T maps to NM_003227.3 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr3:195782028 C>T maps to NM_001128148.1 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr3:195802069 G>A maps to NM_001128148.1 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr3:195778983 G>A maps to NM_001128148.1 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:195785153 C>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr3:195802105 G>A maps to NM_001128148.1 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr8:133941429 C>T maps to NM_003235.4 C1603C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr8:133906094 G>A maps to NM_003235.4 P974P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr8:134042189 C>T maps to NM_003235.4 G2387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:133879286 C>A maps to NM_003235.4 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:133880418 C>T maps to NM_003235.4 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:133945804 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr8:134034364 C>A maps to NM_003235.4 R2336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr8:134034345 C>T maps to NM_003235.4 I2329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:133879280 C>T maps to NM_003235.4 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:134108560 C>T maps to NM_003235.4 L2506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr8:133925508 C>T maps to NM_003235.4 C1459C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr8:133894152 C>T maps to NM_003235.4 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr8:133995658 T>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:95230272 C>A maps to NM_014305.2 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr16:31485479 C>A maps to NM_001042454.2 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:218578610 C>T maps to NM_001135599.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:76446912 G>A maps to NM_003239.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:76425589 C>T maps to NM_003239.2 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr5:135382961 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:101900190 G>T maps to NM_004612.2 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:101900372 T>G did not map to a codon.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr9:101891296 T>C maps to NM_004612.2 C86C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr9:101904816 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr9:101908872 C>T maps to NM_004612.2 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr3:30691946 C>G maps to NM_001024847.2 S175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:92224292 C>T maps to NM_003243.4 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:92181852 G>A maps to NM_003243.4 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr1:92178018 C>T maps to NM_003243.4 R649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:92184930 G>A maps to NM_003243.4 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr2:105900800 G>A maps to NM_004257.4 Q365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:105885989 G>C maps to NM_004257.4 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr2:105924161 C>T maps to NM_004257.4 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr2:105924671 G>T maps to NM_004257.4 C29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:105889360 C>T maps to NM_004257.4 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr20:35207316 C>G maps to NM_021809.6 S47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr20:35207316 C>A maps to NM_021809.6 S47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr23:89177392 T>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:89177537 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr23:89177510 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr23:89177498 G>A did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr23:89177628 A>T did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr23:89177429 C>T did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr23:89177642 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr23:89177636 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr24:3447347 G>A did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr14:24729202 C>G maps to NM_000359.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr14:24731537 G>A maps to NM_000359.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr14:24727512 G>A maps to NM_000359.2 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr20:36758656 C>T maps to NM_004613.2 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr20:36789840 G>A maps to NM_004613.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr20:36760816 G>A maps to NM_004613.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr20:2320504 G>A maps to NM_003245.3 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr20:2290920 C>A maps to NM_003245.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:44935096 C>T maps to NM_003241.3 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr3:44943288 G>C maps to NM_003241.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr15:43559035 A>T did not map to a codon.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr15:43552709 G>A maps to NM_201631.3 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr15:43531078 G>A maps to NM_201631.3 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr15:43531156 A>C maps to NM_201631.3 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr15:43548884 C>G did not map to a codon.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr20:2413264 C>T maps to NM_198994.2 I699I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:2413154 C>T maps to NM_198994.2 Q663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr20:2377243 C>T maps to NM_198994.2 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr20:2413167 C>A maps to NM_198994.2 S667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr20:2381024 G>C maps to NM_198994.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr20:2381072 G>C maps to NM_198994.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr15:43585111 G>A maps to NM_052955.2 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr15:43571898 C>T maps to NM_052955.2 Q534Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr2:85554469 C>A maps to ENST00000409015 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAME-01A-12D-A42E-08 chr2:85554632 C>T maps to ENST00000409015 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr8:56698425 G>A maps to NM_024831.6 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr11:2189112 G>A maps to NM_199292.2 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr11:2186499 G>A maps to NM_199292.2 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr2:43798959 C>G maps to ENST00000330266 R650R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:43458381 G>C maps to ENST00000330266 S1857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr2:43801787 A>G maps to ENST00000330266 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:43458298 G>A maps to ENST00000330266 Q1885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:43801741 G>A maps to ENST00000330266 Q488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr2:43819158 G>A maps to ENST00000330266 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr2:43801712 G>C maps to ENST00000330266 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr2:43458260 C>T maps to ENST00000330266 V1897V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-A1A3-01A-11D-A13W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr16:67876801 G>A maps to NM_020457.2 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr16:67877393 G>T maps to NM_020457.2 G313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr16:67876897 G>T maps to NM_020457.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:72068071 C>G maps to NM_031435.3 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr1:6688687 A>C maps to NM_001195753.1 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr2:242572548 G>A maps to NM_015963.5 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr7:108205228 C>T maps to NM_001130475.1 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr7:108204814 C>T maps to NM_001130475.1 Q336Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr4:76440730 G>A maps to NM_144721.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr22:21354420 G>A maps to NM_030573.2 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr22:21355678 C>G maps to NM_030573.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr22:21354169 C>T maps to NM_030573.2 *310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:36526494 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7S-01A-11D-A391-08 chr4:83839668 G>A maps to NM_024672.4 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr4:83827688 G>A maps to NM_024672.4 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr4:83839947 G>A maps to NM_024672.4 E861E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr15:39881461 G>A maps to NM_003246.2 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr15:39875828 G>A maps to NM_003246.2 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr15:39886598 C>T maps to NM_003246.2 Q1155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr15:39885655 G>A maps to NM_003246.2 R1018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:169648583 G>A maps to NM_003247.2 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr6:169632245 G>A maps to NM_003247.2 H660H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:155172608 G>A maps to NM_007112.3 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:155177628 G>A maps to NM_007112.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:155165786 G>A maps to NM_007112.3 R935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr5:79366560 C>A maps to NM_003248.4 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr5:79375840 G>A maps to NM_003248.4 W875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr5:79372746 C>A maps to NM_003248.4 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:374360 C>T maps to NM_016585.3 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr19:375874 G>A maps to NM_016585.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr19:371296 G>T maps to NM_016585.3 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr19:367155 C>T maps to NM_016585.3 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr1:151849487 G>C maps to NM_053055.3 S224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:151861805 G>A maps to NM_053055.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:151860783 G>A maps to NM_053055.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr6:128134426 G>A maps to NM_001164685.1 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:128134111 C>T maps to NM_001164685.1 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr5:157166349 G>T maps to NM_017872.3 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr10:25312523 A>T maps to NM_024838.4 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr10:25312421 C>A maps to NM_024838.4 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr2:88482314 C>T maps to NM_018271.3 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr23:122799554 G>C did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:122748015 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr23:122753269 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr23:122756964 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr23:122754807 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:122756954 C>G did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:122772796 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:122778430 G>A did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr23:122761691 G>C did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr23:122756957 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr23:122866821 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr23:122802114 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:122757986 C>A did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr5:175395179 G>T maps to NM_032361.2 S11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr17:79848566 G>A maps to NM_005782.3 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr17:79847067 G>A maps to NM_005782.3 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr17:79848580 G>C maps to NM_005782.3 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr17:79848566 G>A maps to NM_005782.3 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:79848596 G>A maps to NM_005782.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:79848600 G>A maps to NM_005782.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr22:29921846 C>T maps to NM_003678.4 L385L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FD-A3SL-01A-21D-A22Z-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr22:29940523 G>C maps to NM_003678.4 Y55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr16:3077425 G>A maps to NM_024339.3 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:3077241 C>T maps to NM_024339.3 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr19:2808384 C>T maps to NM_003249.3 D466D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr3:184090621 C>G maps to NM_000460.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr3:184090546 C>G maps to NM_000460.2 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr17:38244571 C>T maps to NM_003250.5 Y267Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:36752824 C>T maps to NM_005119.3 Q332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:36766617 C>G maps to NM_005119.3 S812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:36748210 C>G maps to NM_005119.3 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr1:36752556 G>C maps to NM_005119.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:36766617 C>G maps to NM_005119.3 S812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr3:24169143 C>T maps to NM_001128177.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr3:24231667 C>T maps to NM_001128177.1 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr11:77775064 G>T maps to NM_003251.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:77775094 C>T maps to NM_003251.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr13:52971454 C>T maps to NM_018676.3 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr13:52952520 G>A maps to NM_018676.3 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr13:52952894 G>A maps to NM_018676.3 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr15:71535005 C>G maps to NM_024817.2 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr15:72039278 G>C maps to NM_024817.2 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr15:72030240 C>T maps to NM_024817.2 R601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr15:71953018 G>T maps to NM_024817.2 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr7:11521430 G>T maps to ENST00000423059 A667A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:11468660 C>G maps to ENST00000423059 G1052G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr7:11676127 C>G maps to ENST00000423059 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr7:11501770 C>A did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr2:137814068 G>T maps to ENST00000272643 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr2:138414423 T>C maps to ENST00000272643 D1391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr2:137928488 C>T maps to ENST00000272643 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:137852589 G>A maps to ENST00000272643 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:138163188 C>G maps to ENST00000272643 S836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:138163372 C>G maps to ENST00000272643 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr2:138208466 C>T maps to ENST00000272643 S1004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr16:20748489 C>T maps to ENST00000431224 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr16:20749187 G>C maps to ENST00000431224 S252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr16:20749187 G>C maps to ENST00000431224 S252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr16:20748427 G>C maps to ENST00000431224 S365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr2:39964111 A>T maps to NM_025264.4 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr2:39964199 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr3:9426370 G>A maps to NM_015453.2 *508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr3:9424927 C>T maps to NM_015453.2 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:9416327 C>G maps to NM_015453.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr3:9425934 T>C maps to NM_015453.2 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr3:9426234 C>T maps to NM_015453.2 R463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr11:134120219 G>C maps to NM_199298.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr11:134118853 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr10:121338339 C>A maps to NM_001033925.1 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr21:32519264 G>C maps to NM_003253.2 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr21:32519222 G>T maps to NM_003253.2 V1155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr21:32617836 G>A maps to NM_003253.2 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr21:32598145 T>A maps to NM_003253.2 K569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr21:32575280 T>C maps to NM_003253.2 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr21:32525012 C>A maps to NM_003253.2 E1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr21:32582411 C>T maps to NM_003253.2 T779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr21:32638733 G>C maps to NM_003253.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr21:32617923 G>A maps to NM_003253.2 N488N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr21:32624118 C>T maps to NM_003253.2 K450K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr21:32582456 G>A maps to NM_003253.2 F764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr6:155458564 C>T maps to ENST00000456144 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:155574086 G>A maps to ENST00000456144 S1404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:155575143 G>A maps to ENST00000456144 T1450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr6:155450770 C>T maps to ENST00000456144 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr6:155500277 G>A did not map to a codon.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr6:155451166 C>T maps to ENST00000456144 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr6:155565883 C>T maps to ENST00000456144 D1170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr6:155569162 C>T maps to ENST00000456144 L1228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr6:155451319 A>G maps to ENST00000456144 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:4816628 G>C maps to NM_182919.2 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr19:4817271 G>C maps to NM_182919.2 S373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr19:4817686 G>A maps to NM_182919.2 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:4817057 G>A maps to NM_182919.2 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:43774765 C>T maps to NM_005424.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr1:43779504 C>T maps to NM_005424.2 Q759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr1:43778093 C>T maps to NM_005424.2 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr1:43778255 G>A maps to NM_005424.2 V637V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr1:43778031 C>T maps to NM_005424.2 R563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr1:43770759 C>T maps to NM_005424.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:113199377 A>G maps to NM_052864.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:134785490 G>A maps to NM_001099221.1 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:90034835 C>T maps to NM_145715.2 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr4:90034852 C>G maps to NM_145715.2 S243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr4:90034941 C>T maps to NM_145715.2 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr4:90034310 C>A maps to NM_145715.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr11:65123926 C>G maps to NM_145719.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr11:65123926 C>T maps to NM_145719.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr4:153691875 C>T maps to NM_145720.2 W94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:153691553 G>A maps to NM_145720.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr4:153691891 C>A maps to NM_145720.2 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr4:153691919 C>T maps to NM_145720.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr8:144680315 C>T maps to NM_032862.4 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:149375649 C>A maps to NM_030953.2 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr5:149375674 A>G maps to NM_030953.2 D79D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr16:3350413 C>T maps to NM_033208.3 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr16:3350599 C>T maps to NM_033208.3 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:156375435 G>A maps to NM_138379.2 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr5:156381552 C>T maps to NM_138379.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr5:156381552 C>T maps to NM_138379.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr12:56822357 C>G maps to NM_003920.3 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr12:56822692 G>A maps to NM_003920.3 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:56816719 G>C maps to NM_003920.3 V783V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:56817141 G>C maps to NM_003920.3 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:56827389 G>A maps to NM_003920.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr12:56815752 G>A maps to NM_003920.3 R858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr12:56826167 A>G maps to NM_003920.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr12:56818909 C>T maps to NM_003920.3 K535K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:56822357 C>A maps to NM_003920.3 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr12:56826817 G>A maps to NM_003920.3 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:56822755 G>C maps to NM_003920.3 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr12:56817596 G>C maps to NM_003920.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr23:48752376 C>T did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr19:7992107 C>T maps to NM_006351.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:7992541 C>T maps to NM_006351.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr19:8000030 C>G did not map to a codon.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr19:39971573 G>A maps to NM_001001563.1 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr19:39976915 G>A maps to NM_001001563.1 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr19:39972524 C>T maps to NM_001001563.1 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr23:100601507 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr23:100603635 G>C did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr11:111957456 C>G maps to NM_012459.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr23:47442864 G>C did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr17:76866986 G>A maps to NM_003255.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr22:33255168 C>T maps to NM_000362.4 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:12195843 G>A maps to NM_003256.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr6:54173569 C>T maps to NM_014464.3 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr6:54173503 C>T maps to NM_014464.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:32043027 C>T maps to NM_022164.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:32051352 G>A did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr14:24710510 C>A maps to NM_001099274.1 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr14:24710486 G>A maps to NM_001099274.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:156396115 C>T maps to NM_015508.4 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:156395593 G>A maps to NM_015508.4 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr11:126162882 C>T maps to NM_148910.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr15:30011183 G>A maps to NM_003257.3 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr15:30019029 C>A maps to NM_003257.3 E756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr15:30064301 G>A maps to NM_003257.3 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr15:30011020 G>A maps to NM_003257.3 Q1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr15:30008846 C>T maps to NM_003257.3 Q1390Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr9:71844145 T>G maps to NM_004817.3 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:71836032 C>T maps to NM_004817.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr9:71844152 G>T maps to NM_004817.3 E503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:3747940 C>T maps to NM_014428.1 D857D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr19:3735873 C>G maps to NM_014428.1 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr19:3746559 C>G maps to NM_014428.1 V729V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:3746487 G>A maps to NM_014428.1 K705K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr17:76182884 C>T maps to NM_003258.4 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:76171136 C>T maps to NM_003258.4 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr17:76171687 G>A maps to NM_003258.4 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr3:53269120 G>A maps to ENST00000423516 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr3:53275177 G>A maps to ENST00000423516 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr23:153549219 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr23:153543531 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr23:153524333 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:153557915 C>T did not map to a codon.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr23:153539539 C>T did not map to a codon.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr23:153539540 A>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:153541020 C>A did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:153543679 A>G did not map to a codon.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr23:153539295 G>C did not map to a codon.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr4:164393314 G>A maps to NM_032136.4 D524D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr4:164394637 G>C maps to NM_032136.4 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:27051728 G>C maps to NM_138463.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr9:84200567 G>A maps to NM_005077.3 I660I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr9:84200558 C>T maps to NM_005077.3 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr9:84235444 G>A maps to NM_005077.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr9:84202673 C>G maps to NM_005077.3 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr9:84268899 G>A maps to NM_005077.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr9:84205814 G>A maps to NM_005077.3 Y578Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:3017852 C>T maps to NM_003260.4 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:3005849 G>A maps to NM_003260.4 I539I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr19:3014581 G>A maps to NM_003260.4 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:70347432 G>T maps to NM_005078.2 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr15:70358415 G>A maps to NM_005078.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr9:82267575 A>G maps to ENST00000376537 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr9:82335205 G>A maps to ENST00000376537 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:2987902 G>A maps to NM_001143986.1 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:2993566 G>A maps to NM_001143986.1 K508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr19:2991961 G>T maps to NM_001143986.1 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr19:2989612 C>T maps to NM_001143986.1 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr19:2989723 C>T maps to NM_001143986.1 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr19:2987369 G>A maps to NM_001143986.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:171913056 G>C maps to ENST00000360843 S179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:171906325 C>T maps to ENST00000360843 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr2:171913025 G>A maps to ENST00000360843 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr2:172016854 C>T maps to ENST00000360843 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:171871389 C>T maps to ENST00000360843 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:60613530 C>A maps to ENST00000326270 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr4:167020553 C>T maps to ENST00000507499 R951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr4:167020651 G>T maps to ENST00000507499 V983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr4:166935683 A>T maps to ENST00000507499 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr4:166924644 G>A maps to ENST00000507499 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr4:167020455 C>G maps to ENST00000507499 S918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:98144395 G>A maps to NM_012465.3 F714F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr10:98155022 C>T maps to NM_012465.3 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr10:98155023 G>T maps to NM_012465.3 S549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:98145843 G>A maps to NM_012465.3 Q661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr10:98273427 A>G maps to NM_012465.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr10:98188404 G>A maps to NM_012465.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr9:35697853 C>T maps to NM_006289.3 K2520K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr9:35703792 C>T maps to NM_006289.3 W2112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:35700301 G>A maps to NM_006289.3 I2182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:35703834 C>T maps to NM_006289.3 T2098T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr9:35714608 G>A maps to NM_006289.3 Q983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr9:35714247 C>T maps to NM_006289.3 T1036T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr15:63008573 G>C maps to NM_015059.2 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:63125737 C>A maps to NM_015059.2 I2346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr15:63069039 G>A maps to NM_015059.2 L1815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr15:63097944 G>C maps to NM_015059.2 L2208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr15:63009827 G>A maps to NM_015059.2 Q939Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr15:63128202 C>G maps to NM_015059.2 S2435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr15:63014625 G>T maps to NM_015059.2 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr15:63131164 G>A maps to NM_015059.2 V2495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr15:63009809 G>A maps to NM_015059.2 Q933Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr15:63029146 G>A maps to NM_015059.2 S1143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr4:38799738 C>T maps to NM_003263.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr4:38774976 C>G maps to NM_030956.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:38776989 C>G maps to NM_030956.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:38776532 G>A maps to NM_030956.3 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr4:154625828 G>A maps to NM_003264.3 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr4:154625549 C>G maps to NM_003264.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr4:154626068 C>T maps to NM_003264.3 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr4:186997898 G>A maps to NM_003265.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr4:187004825 C>T maps to NM_003265.2 N662N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr4:187004577 G>T maps to NM_003265.2 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr4:187004098 C>G maps to NM_003265.2 S420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr9:120475519 C>T maps to NM_138554.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr9:120475701 C>T maps to NM_138554.3 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr9:120470956 C>G maps to NM_138554.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr9:120475510 G>T maps to NM_138554.3 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr9:120475596 G>T maps to NM_138554.3 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr9:120475508 C>A maps to NM_138554.3 S368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr9:120475131 A>G maps to NM_138554.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr4:38830142 G>A maps to NM_006068.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr4:38830533 C>T maps to NM_006068.3 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr23:12905874 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:12906157 C>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:12904544 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr23:12906194 G>A did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:12904759 G>C did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:12905269 A>T did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr23:12903774 G>T did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr23:12903874 C>A did not map to a codon.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr23:12906300 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:12904975 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr23:12904484 T>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr23:12939372 G>C did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr23:12939591 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr23:12937403 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr23:12938247 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr23:12938563 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr23:12937239 A>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:12938894 T>G did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr23:12938506 C>G did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr23:12939699 G>C did not map to a codon.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr23:12940173 T>C did not map to a codon.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr23:12939548 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr23:12939150 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:12938347 T>C did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:12938525 C>G did not map to a codon.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr3:52256621 G>A maps to ENST00000494383 F723F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr3:52255370 G>C maps to ENST00000494383 L1140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:52256255 C>T maps to ENST00000494383 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr3:52257728 G>A maps to ENST00000494383 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr3:52257698 G>A maps to ENST00000494383 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr10:102896498 C>A maps to NM_005521.3 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr2:74742838 G>A maps to NM_016170.4 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr2:74743160 C>T maps to NM_016170.4 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr2:74742967 G>C maps to NM_016170.4 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr5:170738599 G>A maps to NM_021025.2 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr5:170738556 G>A maps to NM_021025.2 W277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr1:62190663 C>T maps to ENST00000371180 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr3:149089638 G>C maps to ENST00000383054 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr3:149048194 T>C maps to NM_138786.3 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr3:196054401 C>G maps to NM_138461.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr2:228228661 A>T maps to NM_024795.3 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr17:4686286 G>C maps to NM_003963.2 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr17:4675345 C>T maps to NM_003963.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr15:83776473 C>T maps to NM_023003.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:19375595 G>A maps to NM_001001524.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr19:19381073 G>T maps to NM_001001524.2 Y103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:19375541 A>C maps to NM_001001524.2 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:19378830 G>A maps to NM_001001524.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr11:64882294 C>T maps to NM_003273.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr11:64882276 C>G maps to NM_003273.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:27148172 G>A maps to NM_016551.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:105361097 C>A maps to NM_030788.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr8:105367187 C>T maps to NM_030788.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr8:105361289 C>A maps to NM_030788.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr8:105361367 C>T maps to NM_030788.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr14:24658938 G>A maps to NM_006405.5 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr13:100153955 G>A maps to NM_004800.1 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr10:98290307 G>A maps to NM_020123.3 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr10:98307746 C>T did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr10:98312795 G>A maps to NM_020123.3 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr10:98312816 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr20:30746280 C>T maps to NM_014742.3 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr20:30753234 G>A maps to NM_014742.3 V639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr20:30753245 G>C maps to NM_014742.3 *643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr20:30753204 C>A maps to NM_014742.3 Y629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr20:30734594 G>C maps to NM_014742.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr20:30738662 G>A maps to NM_014742.3 K410K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr2:219144769 C>T maps to NM_022152.4 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr2:219144823 C>T maps to NM_022152.4 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr2:219146759 C>T maps to NM_022152.4 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr12:50149464 G>C maps to NM_001098576.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr12:50135933 T>A maps to NM_001098576.1 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr12:50152505 C>A maps to NM_001098576.1 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr9:75366835 C>T maps to NM_138691.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr9:75387465 C>G maps to NM_138691.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr9:75435901 C>T maps to NM_138691.2 Y636Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr9:75420350 C>T maps to NM_138691.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr20:2596781 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr20:2591186 C>G maps to NM_080751.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr15:81636365 G>A maps to ENST00000454937 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:81660669 C>T did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr15:81625497 A>T maps to ENST00000454937 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr15:81636347 G>A maps to ENST00000454937 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr15:81650548 C>T maps to ENST00000454937 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr15:81664942 C>T maps to ENST00000454937 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:54667457 G>A maps to NM_001145303.1 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:54666431 G>A maps to NM_001145303.1 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:54665849 G>A maps to NM_001145303.1 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr19:54666463 G>A maps to NM_001145303.1 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr19:54666812 C>A maps to NM_001145303.1 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr19:54666458 G>C maps to NM_001145303.1 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:54664709 G>A maps to NM_001145303.1 I632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr19:54676797 C>G maps to NM_001145303.1 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr19:54664721 G>A maps to NM_001145303.1 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr19:54666422 G>A maps to NM_001145303.1 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr16:19475148 C>T maps to NM_001105248.1 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr16:19483525 C>A maps to NM_001105248.1 C633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr16:19475232 A>T maps to NM_001105248.1 K458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:76113905 G>C maps to NM_007267.6 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:76115384 G>A maps to NM_007267.6 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:76113592 C>G maps to NM_007267.6 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr17:76113637 C>T maps to NM_007267.6 A703A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr17:76122886 G>A maps to NM_007267.6 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr17:76120184 G>A maps to NM_007267.6 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr17:76120739 G>C maps to NM_007267.6 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr16:19020680 C>A maps to NM_024847.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:19041667 G>A maps to NM_024847.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr16:19058552 C>T maps to NM_024847.3 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr16:19058552 C>A maps to NM_024847.3 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:76134244 C>T maps to NM_152468.4 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:76134202 C>G maps to NM_152468.4 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr17:76133859 C>G maps to NM_152468.4 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr17:76130590 T>G maps to NM_152468.4 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:129373851 T>A maps to NM_001017395.3 K536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:129389915 G>A maps to NM_001017395.3 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr1:205240949 G>T maps to NM_014858.3 E610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6X-01A-12D-A42E-08 chr1:205238772 C>T maps to NM_014858.3 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:94965381 G>A maps to NM_020698.2 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr12:94965477 C>T maps to NM_020698.2 K389K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr13:114202655 G>A maps to NM_017905.4 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr13:114202740 C>T maps to NM_017905.4 R632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr13:114202700 C>T maps to NM_017905.4 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr13:114150041 G>A maps to NM_017905.4 W49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:20107203 C>T maps to NM_181719.4 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:20107214 G>A maps to NM_181719.4 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr1:20107214 G>A maps to NM_181719.4 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr15:38233869 A>T did not map to a codon.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr5:140023451 G>T maps to ENST00000252100 E342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr5:140024590 C>T maps to ENST00000252100 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr5:140024594 C>G maps to ENST00000252100 S471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr5:140023481 C>T maps to ENST00000252100 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr5:140021487 C>G maps to ENST00000252100 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr5:140023169 C>T maps to ENST00000252100 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:68909057 G>A maps to NM_024562.1 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:68961656 C>T maps to NM_024562.1 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr16:68877570 G>C maps to NM_024562.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr19:10945677 C>A maps to NM_006858.2 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr15:79614490 C>T maps to NM_007364.2 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr15:79606304 C>T maps to NM_007364.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr7:44619137 G>A maps to NM_182547.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr7:44621646 G>A maps to NM_182547.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr7:44620693 T>G maps to NM_182547.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:44620712 C>T maps to NM_182547.2 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:93622009 G>A maps to NM_016040.4 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr16:69377324 C>T maps to NM_144676.3 K236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr16:69377381 G>A maps to NM_144676.3 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr5:114917012 C>T did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr14:77808331 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr14:77810142 C>T maps to NM_213601.1 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr9:103312380 A>T maps to NM_001198812.1 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:193049158 C>T maps to NM_016192.2 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr2:193049176 G>T maps to NM_016192.2 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr2:192818460 A>T maps to NM_016192.2 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:53798056 G>C maps to NM_001099640.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr17:42092224 G>A maps to NM_032376.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr17:7339221 G>A maps to NM_178518.2 W11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr17:7340338 C>T maps to NM_178518.2 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr17:72781646 C>T maps to NM_017728.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:72832681 C>T maps to NM_017728.3 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr17:72787093 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr17:72787116 G>A maps to NM_017728.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr17:72815896 C>T maps to NM_017728.3 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr17:79287596 G>A maps to NM_178520.3 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr12:48360479 G>A maps to NM_001143842.1 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr12:48360996 C>T maps to NM_001143842.1 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:133099152 C>T maps to NM_001136469.1 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:133099610 C>A maps to NM_001136469.1 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr3:133099307 G>A maps to NM_001136469.1 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:133099946 G>C maps to NM_001136469.1 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:10015337 G>A maps to NM_018447.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr3:10028276 G>A maps to NM_018447.2 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr3:10016099 C>T maps to NM_018447.2 W127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:50396205 C>A maps to NM_007024.4 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr3:50395960 G>A maps to NM_007024.4 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr12:112374513 G>A maps to NM_001193531.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr12:44782334 G>A maps to NM_032256.1 E475E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:108985793 C>T maps to NM_181724.2 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr12:108985558 C>A maps to NM_181724.2 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr7:75616573 G>C maps to NM_031925.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr12:122199640 C>G maps to NM_001080825.2 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr12:122199596 C>A maps to NM_001080825.2 Y168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr11:102319576 A>G maps to NM_052932.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:102272881 C>T maps to NM_052932.2 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr2:96930909 G>A maps to NM_017849.3 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr2:98419202 G>C maps to NM_015348.1 S818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr2:98422017 G>C maps to NM_015348.1 S735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr2:98408978 C>T maps to NM_015348.1 A1338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr2:98408978 C>T maps to NM_015348.1 A1338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr2:98375508 G>A maps to NM_015348.1 F1738F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:98428949 G>A maps to NM_015348.1 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr11:60695124 C>T maps to NM_017870.3 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:60703932 C>T maps to NM_017870.3 Q877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:60692158 C>T maps to NM_017870.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:126128758 G>A maps to NM_052907.2 Q520Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr12:126138269 G>T maps to NM_052907.2 E751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr12:125834310 C>T maps to NM_052907.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr12:125834166 C>T maps to NM_052907.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr12:126128689 G>A maps to NM_052907.2 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr12:125834736 C>A maps to NM_052907.2 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr12:130185154 C>T maps to NM_133448.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47W-01A-11D-A23U-08 chr12:129569226 G>A maps to NM_133448.2 Y488Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:129563189 G>A maps to NM_133448.2 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr12:129822268 G>A maps to NM_133448.2 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:129566552 C>T maps to NM_133448.2 E558E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr12:129559421 C>T maps to NM_133448.2 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr12:129694163 C>A maps to NM_133448.2 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:32964389 C>T maps to NM_207313.1 T698T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr17:32957082 C>T maps to NM_207313.1 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr17:32964997 C>A maps to NM_207313.1 S901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr17:32953554 C>T maps to NM_207313.1 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr17:32963156 G>C maps to NM_207313.1 G613G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr7:142983918 T>C maps to NM_153345.1 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr7:134849591 C>A maps to NM_018295.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr19:48867178 G>A did not map to a codon.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr19:48866598 G>A maps to NM_018273.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr19:48866577 G>A maps to NM_018273.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:42827850 C>T maps to ENST00000406159 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr19:42818479 C>T maps to ENST00000406159 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:5745939 C>G maps to NM_152784.3 S225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr19:5778497 C>T maps to NM_152784.3 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:5745952 C>A maps to NM_152784.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:5724872 G>A maps to NM_152784.3 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr19:5727328 C>A maps to NM_152784.3 C59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr19:5772909 C>T maps to NM_152784.3 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:5733906 C>A maps to NM_152784.3 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr19:36037608 G>C maps to NM_032635.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:36230989 C>T did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr6:10730883 C>T maps to NM_016462.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr3:152058459 C>T maps to NM_001123228.1 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr2:85826216 C>T maps to NM_001031738.2 E266E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr2:85827498 G>A maps to NM_001031738.2 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:55824328 G>A maps to NM_001085488.1 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:55828286 G>A maps to NM_001085488.1 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr19:55828286 G>A maps to NM_001085488.1 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr19:55824343 G>C maps to NM_001085488.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr19:55831792 G>T maps to NM_001085488.1 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr19:55831948 G>T maps to NM_001085488.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:55824271 G>A maps to NM_001085488.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr19:55831948 G>T maps to NM_001085488.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr4:83411349 C>T maps to NM_001080506.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr11:66061852 C>T maps to NM_153266.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr4:153573936 C>A maps to NM_152680.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:21172531 C>G maps to ENST00000451578 S10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr19:19231583 G>C maps to NM_017814.1 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr5:87493534 C>T maps to NM_153354.3 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr2:135308214 G>A maps to NM_030923.4 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:109416483 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:109416480 A>C did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr23:109416576 C>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:109247193 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:109416568 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr23:109416666 G>C did not map to a codon.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr4:56284048 T>A maps to NM_018475.3 L230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:216965209 C>G maps to NM_138390.3 S280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr16:75485606 C>T maps to NM_145254.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr5:72419556 C>T maps to NM_173490.6 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr5:72469402 G>A maps to NM_153217.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr5:72469435 C>T maps to NM_153217.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr4:951683 G>T maps to NM_032326.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr4:951665 C>T maps to NM_032326.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr4:941637 C>T maps to NM_032326.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr4:949203 G>A maps to NM_032326.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:120439082 C>T maps to NM_030577.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:120438761 G>A maps to NM_030577.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr2:39934285 C>T maps to NM_152390.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:39893155 C>G maps to NM_152390.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr14:105061492 G>A maps to NM_207379.1 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr11:62557491 C>T maps to NM_199337.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr11:62557437 A>G maps to NM_199337.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:62557517 G>A maps to NM_199337.2 *220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr6:159046149 C>T maps to NM_020823.1 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr6:159046173 C>T maps to NM_020823.1 Y468Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr6:159049442 C>T maps to NM_020823.1 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr6:159006375 C>T maps to NM_020823.1 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:103431276 C>A maps to NM_144632.3 Y180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr7:1594928 C>T maps to NM_001097620.1 W64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr7:1594934 G>A maps to NM_001097620.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr22:38617496 G>A maps to NM_012264.4 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr4:148552572 T>A maps to NM_018241.2 Y232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr16:8890051 C>G maps to NM_015421.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr23:153247636 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr23:153248181 C>A did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:153247905 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:153248158 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr23:153247909 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr20:48699388 G>A maps to NM_199203.2 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr4:166024205 G>A maps to NM_001100389.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr12:57472423 G>A maps to NM_001130963.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:15601350 T>C maps to NM_001004320.1 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr7:15427048 G>A maps to NM_001004320.1 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr7:15470659 T>C maps to NM_001004320.1 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr2:220414542 G>A maps to NM_001005209.1 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:26684872 C>A maps to ENST00000457710 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr17:26684893 G>C maps to ENST00000457710 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:74319521 G>C maps to NM_013390.2 V1061V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:74345052 G>A maps to NM_013390.2 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr9:74319521 G>C maps to NM_013390.2 V1061V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:74355057 C>A maps to NM_013390.2 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr9:74365247 G>C maps to NM_013390.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr10:95661186 C>G maps to NM_001134658.1 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr10:95658334 G>A maps to NM_001134658.1 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr10:95661012 C>G maps to NM_001134658.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr6:130762700 C>G maps to NM_052913.2 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr6:130762433 A>G maps to NM_052913.2 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:9662347 G>C maps to NM_001010866.3 *393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:9662267 T>C maps to NM_001130924.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr15:72699439 C>A maps to NM_001080462.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr15:72699448 C>T maps to NM_001080462.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr15:72691085 G>A maps to NM_001080462.1 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr9:140099716 G>A maps to NM_053045.1 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr9:140099689 G>A maps to NM_053045.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr16:1584323 C>G maps to NM_024600.4 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr16:1584326 A>G maps to NM_024600.4 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr19:11456023 G>A maps to NM_198536.2 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr19:11456265 C>G maps to NM_198536.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:212553307 C>G maps to NM_001198862.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr1:212538679 G>A maps to NM_001198862.1 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:212550966 G>T maps to NM_001198862.1 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr3:190158095 G>T maps to NM_207316.1 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr16:67262274 G>A maps to NM_014187.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr7:129832605 C>A maps to NM_032842.3 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr7:138487790 G>T maps to ENST00000422794 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:27259971 C>T maps to NM_017727.4 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:27258519 G>A maps to NM_017727.4 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr2:27261628 G>A maps to NM_017727.4 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr2:27259455 G>A maps to NM_017727.4 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:27260563 G>A maps to NM_017727.4 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr2:27263067 T>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:32784669 C>T maps to NM_212558.2 D163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr9:32784396 C>T maps to NM_212558.2 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:61165261 C>T maps to NM_001173991.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr3:136573340 A>G maps to NM_025246.2 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:136574264 C>G maps to NM_025246.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr3:136573880 T>C maps to NM_025246.2 N193N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:136573736 C>T maps to NM_025246.2 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:10628431 A>G maps to NM_001004313.1 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:27657273 C>T maps to NM_032125.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:62558198 G>A maps to NM_001080501.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr14:67940531 A>G maps to NM_182526.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr16:75579303 C>G maps to NM_001077416.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr16:75579279 C>T maps to NM_001077416.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr11:118403108 C>A maps to NM_032780.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr10:63212713 G>A maps to NM_178505.6 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr10:63170340 G>A maps to NM_178505.6 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr10:63188708 C>A maps to NM_178505.6 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr10:63188708 C>A maps to NM_178505.6 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr10:63212698 G>A maps to NM_178505.6 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr6:75977362 T>C maps to NM_018247.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr6:75970564 T>A maps to NM_018247.3 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr14:61747370 G>T maps to NM_001017970.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr14:61747247 G>A maps to NM_001017970.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr23:102968911 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr23:102968911 C>G did not map to a codon.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr4:41941218 T>C maps to NM_018126.2 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr4:41951360 T>C maps to NM_018126.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:100349617 C>A did not map to a codon.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr23:100349585 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr23:100349627 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:120194517 C>T maps to NM_183240.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr2:120194997 C>T maps to NM_183240.2 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:16790903 C>T maps to NM_024074.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:16798976 C>G maps to NM_024074.1 S232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr9:108483892 G>C maps to NM_018112.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr3:119153694 G>A maps to NM_018266.1 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr3:119176953 G>A maps to NM_018266.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr1:32542401 C>G maps to NM_018056.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:32568162 C>G maps to NM_018056.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr3:185209348 A>G maps to NM_080652.3 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:44905723 G>A maps to NM_144638.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr3:194331643 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr3:194309272 C>G maps to NM_001166305.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr3:194336315 T>C maps to NM_001166305.1 K345K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:100277339 C>T maps to ENST00000403410 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr11:129727290 C>T maps to NM_138788.3 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:129725681 C>T maps to NM_138788.3 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr23:34657460 G>T did not map to a codon.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr1:54291556 G>A maps to NM_018087.4 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:54262802 G>A maps to NM_018087.4 Q413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr1:54238132 A>G maps to NM_018087.4 H610H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:57917166 C>T maps to NM_030938.3 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:64178827 C>G maps to NM_014254.1 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr1:25669468 G>A maps to NM_014313.2 W37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr1:15546237 G>A maps to NM_018022.2 *254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:33363912 C>G maps to NM_033504.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:33363894 C>G maps to NM_033504.2 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr1:33363846 C>G maps to NM_033504.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr1:33363912 C>T maps to NM_033504.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:20928360 G>T maps to NM_001100814.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr14:20928870 G>A maps to NM_001100814.1 N99N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:20928360 G>T maps to NM_001100814.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr14:20927798 C>T maps to NM_001100814.1 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr1:95657183 C>T maps to NM_152487.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:25773321 C>T maps to NM_018202.4 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:54511385 G>A maps to ENST00000371338 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr19:18729067 C>T maps to NM_012109.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr19:18726858 C>T maps to NM_012109.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr19:18727875 C>A maps to NM_012109.2 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:55457706 T>C maps to NM_182532.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:55452005 C>A maps to NM_182532.1 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr1:55452086 C>T maps to NM_182532.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:43476561 G>A maps to NM_024956.3 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr15:43447022 C>T maps to NM_024956.3 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr1:226044657 G>A maps to NM_014698.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:226055672 C>T maps to NM_014698.2 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:226034878 C>T maps to NM_014698.2 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:226055717 G>T maps to NM_014698.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr6:44122427 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:44117967 G>T maps to NM_018426.1 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:77706017 C>T maps to NM_020431.2 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:77712284 C>G maps to NM_020431.2 S484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:77691804 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr14:77706870 C>T maps to NM_020431.2 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr14:77705802 C>T maps to NM_020431.2 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr8:91657401 C>T maps to NM_001008495.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr8:125339645 C>T maps to NM_194291.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr8:29923529 G>C maps to NM_016127.4 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr8:94798571 G>C maps to NM_153704.5 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr8:94822084 G>T maps to NM_153704.5 E912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr8:94805472 G>A maps to NM_153704.5 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr8:56675386 G>C maps to ENST00000434581 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:46159474 G>T maps to NM_016486.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr8:74888563 C>T maps to NM_017866.5 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:133740097 G>A maps to ENST00000395406 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr8:133769484 G>A maps to ENST00000395406 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:45430143 G>C maps to NM_001123376.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr10:45430458 C>T maps to NM_001123376.1 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:109797207 G>C maps to NM_153015.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:156256051 G>A maps to NM_032323.2 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr1:156255358 C>T maps to NM_032323.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr1:156255628 G>T maps to NM_032323.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:156255263 C>T maps to NM_032323.2 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:703011 C>T maps to ENST00000449452 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:703074 C>T maps to ENST00000449452 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:702999 C>T maps to ENST00000449452 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:16073401 G>A maps to NM_001013641.1 Q266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr15:34520650 C>A maps to NM_016454.2 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr15:34519943 C>T maps to NM_016454.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr15:34520657 G>A maps to NM_016454.2 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr15:42512272 C>A maps to ENST00000389834 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr15:42565479 C>A maps to ENST00000389834 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr2:112838675 C>G maps to NM_032824.2 S212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:112858207 C>T maps to NM_032824.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr2:112863602 C>G maps to NM_032824.2 S492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:112838973 C>G maps to NM_032824.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:7758848 C>T maps to NM_203411.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr16:424316 G>A maps to NM_021259.2 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr16:427569 G>A maps to NM_021259.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:425417 C>T maps to NM_021259.2 E414E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr9:35846973 C>T maps to ENST00000360192 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FM-01A-11D-A38G-08 chr9:136384091 G>A maps to NM_001080483.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:136380648 G>A maps to NM_001080483.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:24646109 C>T maps to NM_024893.1 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr20:24523846 T>A maps to NM_024893.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:41884360 C>T maps to NM_001098821.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr17:48356557 G>A maps to NM_153229.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:26652668 C>T maps to NM_014573.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr17:26646321 C>T maps to NM_014573.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr17:26653743 C>T maps to NM_014573.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr17:38991463 C>T maps to NM_001195386.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:69088120 C>A maps to NM_007114.2 E623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr3:69087846 G>A maps to NM_007114.2 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr3:69082819 C>T maps to NM_007114.2 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:28652038 C>T maps to NM_206832.1 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAME-01A-12D-A42E-08 chr17:28656431 G>A maps to NM_206832.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr23:154743711 G>T did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr23:154743793 G>T did not map to a codon.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr23:154736680 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr9:100353571 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr15:52074979 G>A maps to NM_014548.3 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr15:52090494 G>A maps to NM_014548.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr15:52074916 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr15:52069162 A>T maps to NM_014548.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr15:52186129 G>A maps to NM_014547.4 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr12:98938016 C>T maps to NM_001032283.2 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr3:33134910 G>A maps to NM_001039770.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr4:68810290 G>A maps to NM_182606.3 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr4:68777185 C>G maps to NM_182606.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr4:68691545 A>G maps to NM_004262.2 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr4:69343317 G>A maps to NM_014058.3 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr4:69337204 T>C maps to NM_014058.3 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr4:68919642 G>C maps to NM_207407.2 S434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr4:68964664 A>G maps to NM_207407.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr4:68934363 G>A maps to NM_207407.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr4:68919737 G>A maps to NM_207407.2 Y402Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr12:51279032 C>T maps to NM_182559.2 N219N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:51279057 G>T maps to NM_182559.2 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:117780579 G>T maps to ENST00000413475 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr11:117787897 C>T maps to ENST00000413475 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr11:117774462 G>A maps to ENST00000413475 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr21:42840424 G>A maps to NM_001135099.1 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr21:42866364 G>A maps to NM_001135099.1 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr21:42845281 C>T maps to NM_001135099.1 W327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WY-01A-11D-A22Z-08 chr21:42839671 G>A maps to NM_001135099.1 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr21:42860360 G>T maps to NM_001135099.1 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr21:43802183 G>C maps to ENST00000380399 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr21:43800262 C>A maps to ENST00000380399 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr21:43803245 C>A maps to ENST00000380399 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:117988105 G>A maps to NM_019894.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr11:117984050 C>T maps to NM_019894.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:117969793 C>T maps to NM_019894.3 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr11:117969811 C>T maps to NM_019894.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr11:117982462 G>A maps to NM_019894.3 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr11:117975520 G>A maps to NM_019894.3 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:113568006 G>A maps to NM_030770.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr22:37482401 G>A maps to ENST00000381792 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:111785290 C>T maps to ENST00000443106 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:111794168 C>G maps to ENST00000443106 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr3:111775978 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:111769516 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr3:111794201 C>T maps to ENST00000443106 I594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr19:2403104 C>T maps to NM_182973.1 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr19:2408524 C>T maps to NM_182973.1 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr19:2408401 C>T maps to NM_182973.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:29757223 C>T maps to NM_001193451.1 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:29736356 T>A maps to NM_001193451.1 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:29667534 T>C maps to NM_001193451.1 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr12:29920925 G>A maps to NM_001193451.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:29786269 C>A did not map to a codon.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr12:29911634 A>T did not map to a codon.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr12:29904708 C>T maps to NM_001193451.1 Q276Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:83455600 G>A maps to NM_152588.1 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr12:83081400 C>T maps to NM_152588.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr12:83290111 G>C maps to NM_152588.1 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:83379826 T>G did not map to a codon.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr12:88568404 G>A maps to NM_181783.3 W407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr13:101287094 G>A maps to NM_032813.2 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr7:150779320 G>C maps to NM_031434.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr7:150779266 C>T maps to NM_031434.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr14:51707162 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:57507578 G>C maps to NM_015959.3 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:66381086 C>A maps to NM_019022.3 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:7980416 G>A maps to NM_021156.2 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr9:117849210 A>G maps to NM_002160.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr9:117797569 C>T maps to NM_002160.2 S1900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:117840338 C>A maps to NM_002160.2 E853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:117840405 G>A maps to NM_002160.2 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr9:117791726 C>G maps to NM_002160.2 L2027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr9:117846584 G>T maps to NM_002160.2 I678I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr9:117804555 C>T maps to NM_002160.2 W1730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr9:117810728 A>G maps to NM_002160.2 N1554N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:31544354 C>T maps to NM_000594.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr6:31544994 C>G maps to NM_000594.2 S128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:31544333 C>T maps to NM_000594.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr17:26666705 C>T maps to NM_021137.4 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr17:26669437 C>T maps to NM_021137.4 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:103593906 C>T maps to NM_006291.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr14:103596085 C>T maps to NM_006291.2 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr6:138199922 G>A maps to NM_006290.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr6:138198246 G>A maps to NM_006290.2 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:152222732 T>C did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:118728703 C>T maps to NM_014350.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr5:118728865 C>T maps to NM_014350.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr1:151131259 C>G maps to NM_024575.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr1:151131664 C>T maps to NM_024575.3 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr15:51397238 G>A maps to NM_207381.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr15:51350440 C>G maps to NM_207381.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr15:51350512 G>A maps to NM_207381.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr8:23082520 C>G maps to NM_003844.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr8:23049350 C>T maps to NM_003844.3 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr8:23082526 C>T maps to NM_003844.3 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr8:22885859 C>T maps to NM_003842.4 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr8:22886050 T>A maps to NM_003842.4 K181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr8:22888353 G>A maps to NM_003842.4 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr8:22974540 T>C maps to ENST00000356864 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr8:23003256 G>A maps to NM_003840.3 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr8:23003286 A>G maps to NM_003840.3 Y210Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr8:23003196 G>A maps to NM_003840.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr8:119938730 A>T did not map to a codon.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr8:119938739 G>T maps to NM_002546.3 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr1:2489175 C>T maps to NM_003820.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:2489884 G>T maps to NM_003820.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr13:24243106 T>C maps to NM_018647.2 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr13:24200926 G>A maps to NM_018647.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:6442924 G>A maps to NM_001065.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr1:12262094 G>T maps to NM_001066.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:47254277 G>C maps to NM_014452.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr1:1148064 T>C maps to NM_003327.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr1:1147361 G>T maps to NM_003327.3 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr20:62329777 G>A maps to NM_003823.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:62329777 G>A maps to NM_003823.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:12195643 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr1:12169630 C>T maps to NM_001243.3 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:7460636 C>A maps to NM_003809.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr17:7462454 G>A maps to NM_003808.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr13:108922314 G>A maps to NM_006573.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr9:117568271 C>T maps to NM_005118.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr9:117552902 G>C maps to NM_005118.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:173019956 C>T maps to NM_005092.3 W49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:173019879 C>A did not map to a codon.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:173176221 G>A maps to NM_003326.3 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:117666447 G>A maps to NM_001244.2 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:6531166 G>A maps to NM_003811.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr19:6534929 G>C maps to NM_003811.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr3:170885056 G>T maps to NM_015028.2 S259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr3:170856087 T>C maps to NM_015028.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr3:170945998 G>C maps to NM_015028.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr3:170801983 C>T maps to NM_015028.2 K1043K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:170784512 A>G maps to NM_015028.2 N1237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr3:170843741 G>A maps to NM_015028.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:122075809 C>A maps to ENST00000509841 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr4:122068305 G>A maps to ENST00000509841 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:122078328 G>A maps to ENST00000509841 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr4:122078353 G>C maps to ENST00000509841 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:195615315 C>T maps to NM_001010938.1 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr3:195593872 G>A maps to NM_001010938.1 F1047F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr3:195610066 G>A maps to NM_001010938.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr3:195594700 G>C maps to NM_001010938.1 S886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:195608973 G>A maps to NM_001010938.1 Q342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:195610084 G>A maps to NM_001010938.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr3:195611832 C>T maps to NM_001010938.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr3:195595152 C>A maps to NM_001010938.1 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr11:57087812 G>A maps to NM_033396.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr11:57080262 G>A maps to NM_033396.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr11:57089341 G>A maps to NM_033396.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr11:57077451 C>T maps to NM_033396.2 K911K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr11:57080205 G>A maps to NM_033396.2 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:99854575 C>T did not map to a codon.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr23:99852499 G>C did not map to a codon.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr23:99854639 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr1:175105996 G>A maps to NM_022093.1 A1156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr1:175067711 C>T maps to NM_022093.1 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:175097776 G>A maps to NM_022093.1 Q1075Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:175067636 G>A maps to NM_022093.1 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr1:175066814 G>A maps to NM_022093.1 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr1:175067658 G>T maps to NM_022093.1 E683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:175086246 G>A maps to NM_022093.1 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:175086216 G>A maps to NM_022093.1 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:175116065 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:175049447 G>T maps to NM_022093.1 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:52486245 G>T maps to NM_003280.2 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr3:52486513 C>A maps to NM_003280.2 E14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr20:44453013 C>T maps to NM_003279.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr20:44453227 G>A maps to NM_003279.2 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:1862394 G>C maps to ENST00000381906 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:74835185 C>T maps to NM_001112808.2 C629C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:74737352 C>T maps to NM_001112808.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:55645271 G>A maps to NM_003283.4 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:201332474 C>T maps to ENST00000421663 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr1:201334402 C>G maps to ENST00000421663 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr11:1955620 G>A maps to ENST00000397301 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr5:72199591 C>G maps to NM_002270.3 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr5:72151731 C>T maps to NM_002270.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr5:72161421 G>A did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr5:72192881 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr5:72192384 T>C did not map to a codon.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr19:12821492 G>A maps to NM_001136196.1 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:12826059 G>A maps to NM_001136196.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:12825887 G>A maps to NM_001136196.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:12829858 G>A maps to NM_001136196.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr19:12817069 G>A maps to NM_001136196.1 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr19:12829900 G>A maps to NM_001136196.1 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr7:128640614 C>T maps to ENST00000471166 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr7:128645213 C>A did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr7:128630023 G>A maps to ENST00000471166 Q531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr7:128620039 C>T maps to ENST00000471166 Q669Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr7:128655127 C>A maps to ENST00000471166 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr7:128612602 C>G maps to ENST00000471166 R803R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:175372297 G>A maps to NM_003285.2 Y318Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr1:175324728 G>T maps to NM_003285.2 T1053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:175334311 G>A maps to NM_003285.2 N807N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr1:175365752 G>A maps to NM_003285.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr1:175299341 G>A maps to NM_003285.2 Q1221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr1:175306717 C>G maps to NM_003285.2 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr1:175335227 G>C maps to NM_003285.2 T700T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr7:5399034 G>T maps to NM_001080495.2 I1609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr7:5355626 G>C maps to NM_001080495.2 L2274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr7:5353240 G>C maps to NM_001080495.2 L2427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr7:5417590 G>A maps to NM_001080495.2 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr7:5347937 C>T maps to NM_001080495.2 A2902A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr7:5410926 G>A maps to NM_001080495.2 Q1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr16:24818088 C>T maps to NM_014494.2 F1508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr16:24788435 C>T maps to NM_014494.2 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:24817005 G>A maps to NM_014494.2 L1401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr16:24808845 G>A maps to NM_014494.2 A1199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr16:24802569 C>T maps to NM_014494.2 A869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr16:24820727 C>G maps to NM_014494.2 S1533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr16:24803019 G>A maps to NM_014494.2 V1019V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr16:24816469 C>T maps to NM_014494.2 Q1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:24802033 C>T maps to NM_014494.2 Q691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr16:24805970 T>C maps to NM_014494.2 N1153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr22:40711470 A>T maps to ENST00000454349 S1635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:40662284 C>G maps to ENST00000454349 S698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr22:40662820 C>T maps to ENST00000454349 Q877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:40661276 C>G maps to ENST00000454349 S362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr22:40661967 C>T maps to ENST00000454349 H592H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr22:40660944 T>C maps to ENST00000454349 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:76047218 G>A maps to NM_001142640.1 W692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr17:76047032 G>A maps to NM_001142640.1 W630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr17:76045866 G>T maps to NM_001142640.1 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr2:218696220 C>T maps to NM_022648.4 L985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr2:218674652 G>A maps to NM_022648.4 I1618I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr2:218750466 C>T maps to NM_022648.4 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:218683207 G>A maps to NM_022648.4 Q1179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr7:47408073 G>A maps to NM_022748.11 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr7:47454804 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:47344437 C>T maps to NM_022748.11 R938R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr7:47454779 G>C maps to NM_022748.11 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr7:47408373 G>A maps to NM_022748.11 V623V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr17:38633938 C>T maps to NM_032865.5 E683E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr17:38638603 G>C maps to NM_032865.5 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr6:32021429 G>A maps to ENST00000375244 P2842P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr6:32029943 G>T maps to ENST00000375244 I2386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:32016365 C>T maps to ENST00000375244 V3273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:32046816 G>A maps to ENST00000375244 G1456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr6:32014186 C>T maps to ENST00000375244 V3457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr6:32024426 C>T maps to ENST00000375244 K2693K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr6:32017874 G>A maps to ENST00000375244 V3113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr6:32015616 C>T maps to ENST00000375244 R3406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:32010103 G>A maps to ENST00000375244 F4082F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr6:32035480 G>A maps to ENST00000375244 H2167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr6:32046825 G>A maps to ENST00000375244 S1453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr6:32014153 G>T maps to ENST00000375244 S3468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr6:32029937 C>A maps to ENST00000375244 V2388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr6:32046945 G>T maps to ENST00000375244 P1413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr6:32015751 C>G maps to ENST00000375244 L3361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr6:32065176 C>G maps to ENST00000375244 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr6:32032766 G>A maps to ENST00000375244 F2224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr6:32029324 G>A maps to ENST00000375244 D2447D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:32049999 C>T maps to ENST00000375244 E1183E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr6:32065624 G>T maps to ENST00000375244 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr6:32064744 G>T maps to ENST00000375244 C295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:32016206 G>A maps to ENST00000375244 Y3326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr17:48940622 T>C maps to NM_005749.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr17:48941122 G>A maps to NM_005749.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:48940730 G>C maps to NM_005749.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:48940751 G>A maps to NM_005749.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:48940757 G>A maps to NM_005749.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr22:41833049 G>A maps to NM_016272.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr22:41832967 C>A maps to NM_016272.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr22:41833079 C>T maps to NM_016272.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr22:35726431 C>T maps to ENST00000451197 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr22:35717978 G>A maps to ENST00000451197 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr17:52981123 C>A maps to NM_005486.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr17:52993151 C>A maps to NM_005486.2 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:17772712 G>A maps to NM_001082968.1 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:235292006 G>A maps to NM_014765.2 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr14:58862761 C>G maps to NM_207377.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:43571785 C>T maps to NM_006809.4 Q298Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr20:43571818 G>C maps to NM_006809.4 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr20:43572201 G>A maps to NM_006809.4 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr19:45395665 G>A maps to NM_006114.2 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr1:161197698 G>A maps to NM_032174.4 W135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr9:37592508 G>C maps to NM_001134485.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:100096562 C>A maps to NM_014820.3 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr3:100103343 C>T maps to NM_014820.3 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr20:39704875 C>G maps to NM_003286.2 S74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr8:144411591 A>G maps to NM_052963.1 Y96Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr8:144406278 G>A maps to NM_052963.1 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr3:25665050 C>A maps to ENST00000264331 V894V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr3:25640994 C>T maps to ENST00000264331 R1547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:18210207 G>A maps to NM_004618.3 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr17:18181484 G>A maps to NM_004618.3 N777N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr17:18181343 G>A maps to NM_004618.3 V824V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr17:18188762 T>A maps to NM_004618.3 K557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr22:22322013 C>T maps to NM_003935.3 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:22330075 C>T maps to NM_003935.3 K2K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr22:22327042 G>A maps to NM_003935.3 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr22:22317254 C>T maps to NM_003935.3 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr3:133374176 C>T maps to NM_007027.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:133368326 C>T maps to NM_007027.3 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:32544066 C>T maps to NM_005802.4 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr9:32543098 G>T maps to NM_005802.4 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr9:32542983 C>T maps to NM_005802.4 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47S-01A-11D-A23U-08 chr9:132581154 C>T maps to ENST00000437532 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:132584878 G>C maps to ENST00000437532 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:179883174 C>G maps to ENST00000398836 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:179815352 G>C maps to NM_145034.4 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr9:130496822 G>A maps to NM_001085347.1 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:130494387 G>A maps to NM_001085347.1 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr9:130496589 G>A maps to NM_001085347.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:179054979 C>T maps to NM_022371.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:179057213 C>T maps to NM_022371.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr8:59764333 G>A maps to NM_014729.2 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr8:59872528 C>A maps to NM_014729.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr8:59764172 G>A maps to NM_014729.2 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr8:59764313 C>T maps to NM_014729.2 Q154Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr8:59852046 A>T maps to NM_014729.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr8:59728115 A>G maps to NM_014729.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr20:42695476 G>A maps to ENST00000348077 E497E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr20:42635188 C>A maps to ENST00000348077 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr20:42694695 C>A maps to ENST00000348077 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:42635185 G>A did not map to a codon.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr20:42635356 C>T maps to ENST00000348077 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr16:52480013 G>A maps to ENST00000407228 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr14:21957483 G>A maps to NM_014828.2 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr14:21960462 G>A maps to NM_014828.2 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr17:7574020 C>A maps to NM_001126112.1 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr17:7576885 C>T maps to NM_001126112.1 K320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr17:7579590 C>T did not map to a codon.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr17:7577536 C>T maps to NM_001126112.1 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr17:7577106 A>T maps to NM_001126112.1 C277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr17:7578238 C>A maps to NM_001126112.1 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr17:7578381 G>C maps to NM_001126112.1 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr17:7577121 C>T maps to NM_001126112.1 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr17:7578187 C>A maps to NM_001126112.1 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:7572985 G>A maps to NM_001126112.1 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:7578499 G>A maps to NM_001126112.1 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr17:7578178 C>A maps to NM_001126112.1 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr17:7576851 C>A did not map to a codon.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr17:7578418 C>A maps to NM_001126112.1 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr17:7577078 C>A maps to NM_001126112.1 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:7579528 C>T maps to NM_001126112.1 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr17:7576885 C>T maps to NM_001126112.1 K320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr17:7577076 C>T maps to NM_001126112.1 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr17:7578289 C>T did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr17:7574020 C>A maps to NM_001126112.1 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr17:7573009 T>C did not map to a codon.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:7578381 G>C maps to NM_001126112.1 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr17:7577081 C>A maps to NM_001126112.1 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr17:7576851 C>T did not map to a codon.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr17:7578194 C>T maps to NM_001126112.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr17:7578391 C>A maps to NM_001126112.1 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr17:7578430 G>A maps to NM_001126112.1 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr17:7574020 C>A maps to NM_001126112.1 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr17:7577057 C>A maps to NM_001126112.1 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr17:7576896 G>A maps to NM_001126112.1 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr17:7577084 C>A maps to NM_001126112.1 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr17:7579414 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr17:7578238 C>A maps to NM_001126112.1 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr17:7578492 C>T maps to NM_001126112.1 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMW-01A-11D-A42E-08 chr17:7576890 T>A maps to NM_001126112.1 K319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr17:7574020 C>A maps to NM_001126112.1 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr17:7579323 A>T maps to NM_001126112.1 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:7579484 C>A maps to NM_001126112.1 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr17:7577057 C>A maps to NM_001126112.1 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr17:7579405 G>C maps to NM_001126112.1 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr17:7579853 G>C maps to NM_001126112.1 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr17:7577078 C>A maps to NM_001126112.1 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr11:128807620 G>A maps to NM_022112.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:43739642 G>A maps to NM_001141980.1 I919I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:43773210 T>G maps to NM_001141980.1 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr15:43784618 G>A maps to NM_001141980.1 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr15:43748204 T>C maps to NM_001141980.1 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr15:43784582 G>A maps to NM_001141980.1 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:223981106 C>T maps to NM_001031685.2 E920E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7N-01A-11D-A391-08 chr1:223991954 C>T maps to NM_001031685.2 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr1:223983974 G>A maps to NM_001031685.2 Q756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:223986193 C>T maps to NM_001031685.2 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:223983916 G>T maps to NM_001031685.2 S775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr1:224008928 A>G maps to NM_001031685.2 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:223994609 G>A maps to NM_001031685.2 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:223971978 G>A maps to NM_001031685.2 V1067V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:223983916 G>C maps to NM_001031685.2 S775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:223976730 G>A maps to NM_001031685.2 Q1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr11:44957159 G>A maps to NM_006034.3 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr11:44956506 G>C maps to NM_006034.3 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr17:27899298 C>G maps to NM_138349.2 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr2:24305782 G>A maps to NM_147184.1 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr2:24305842 G>T maps to NM_147184.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr8:95952429 G>C maps to NM_033285.3 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr8:95952398 G>A maps to NM_033285.3 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr8:95952365 G>C maps to NM_033285.3 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr20:33296548 C>T maps to NM_021202.1 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr20:44005931 C>T maps to NM_014477.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr20:44006241 C>T maps to NM_014477.2 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr3:189604228 C>T maps to NM_003722.4 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:189526266 C>T maps to NM_003722.4 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:189612185 C>G maps to NM_003722.4 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr3:189597921 C>T maps to NM_001114979.1 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:189584543 C>T maps to NM_003722.4 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr3:189586404 G>C maps to NM_003722.4 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr3:189608622 G>C maps to NM_003722.4 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr1:3644230 C>T maps to NM_005427.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr1:3640002 G>A maps to NM_005427.2 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr1:3645961 G>A maps to NM_005427.2 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr1:3624129 G>A maps to NM_005427.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr6:83075790 C>T maps to NM_006670.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr6:83075163 C>T maps to NM_006670.4 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr12:113705697 C>T maps to NM_001143819.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr12:113704127 C>T maps to NM_001143819.1 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr12:113710475 C>T maps to NM_001143819.1 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr11:68835029 G>A maps to NM_139075.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:68838872 C>T maps to NM_139075.3 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr11:68835068 C>T maps to NM_139075.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr8:80992660 C>A maps to NM_001025252.1 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr6:125578273 G>A maps to NM_003287.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr20:62505085 C>G maps to NM_199360.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:18057566 C>T maps to ENST00000341556 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:18048080 A>C maps to ENST00000341556 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr11:18057506 A>G maps to ENST00000341556 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr12:72388269 G>A maps to ENST00000389376 K337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:72425081 G>A maps to ENST00000389376 K409K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr12:72372842 C>G maps to ENST00000389376 S312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr12:72335386 A>G maps to ENST00000389376 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr12:72338187 C>T maps to ENST00000389376 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr12:6976717 C>T maps to NM_001159287.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr7:144320257 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:63363287 G>C did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr9:35684255 G>A maps to ENST00000329305 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:154130138 G>C maps to NM_001043351.1 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:154141836 C>T maps to ENST00000328159 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr1:154163691 C>T maps to ENST00000271850 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr1:154142874 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:154130120 C>T maps to NM_001043351.1 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr19:16178466 G>A maps to NM_001145160.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr2:1520730 C>T maps to NM_000547.5 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr2:1499949 G>A maps to NM_000547.5 W732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr2:1460026 G>A maps to NM_000547.5 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr2:1497622 C>T maps to NM_000547.5 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr2:1507831 C>T maps to NM_000547.5 D833D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr2:1459993 C>T maps to NM_000547.5 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr11:6638064 G>C maps to ENST00000453338 S247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr11:6638643 C>G maps to ENST00000453338 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr11:6637564 G>A maps to ENST00000453338 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr11:6636536 C>G maps to ENST00000453338 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr13:103298649 G>A maps to ENST00000376052 V800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr13:103279420 C>A maps to ENST00000376052 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr13:103286386 G>A maps to ENST00000376052 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr13:103301810 C>G maps to ENST00000376052 S976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr13:103268774 T>C maps to ENST00000376052 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr5:677902 C>G maps to NM_007030.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr14:21499233 G>A maps to NM_173846.4 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:67424426 G>A maps to NM_016140.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr16:67424498 G>A maps to NM_016140.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr1:186292874 T>C maps to NM_003292.2 P2080P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:186319406 G>C maps to NM_003292.2 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:186322837 C>T maps to NM_003292.2 E772E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:186296752 C>A maps to NM_003292.2 E1910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr1:186283841 G>A maps to NM_003292.2 Q2319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr1:186325562 G>A maps to NM_003292.2 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr3:127298696 G>C maps to NM_001136053.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr3:127294259 G>A maps to NM_001136053.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:127295477 C>T maps to NM_001136053.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr3:127294071 G>A maps to NM_001136053.1 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:127294059 G>A maps to NM_001136053.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr3:188933082 G>A maps to NM_198485.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr3:188925280 G>C maps to NM_198485.3 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:188925321 C>G maps to NM_198485.3 S50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr3:188925177 C>G maps to NM_198485.3 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr3:188925347 C>T maps to NM_198485.3 Q59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:3544177 G>A maps to NM_182752.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:3542276 G>A maps to NM_182752.3 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr2:73957856 C>A maps to ENST00000409716 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr9:140093629 G>A maps to NM_001128228.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr9:140093441 C>T maps to NM_001128228.2 K574K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr9:140086969 G>A maps to NM_001128228.2 F633F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr16:1291301 G>A maps to ENST00000461509 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr16:1291637 C>G maps to ENST00000461509 S153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr16:1306598 G>C maps to NM_012217.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:65705933 C>T maps to NM_003596.3 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr21:10951348 A>G maps to NM_199261.2 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr21:10934120 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:10933879 G>A maps to NM_199261.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr21:10951281 G>T maps to NM_199261.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr21:10910342 A>T maps to NM_199261.2 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr21:10942750 G>T maps to NM_199261.2 Y230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr21:10944738 A>G maps to NM_199261.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr21:10951327 A>G maps to NM_199261.2 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr21:10920137 C>T maps to NM_199261.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr21:10942759 T>C maps to NM_199261.2 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr21:10920139 T>G maps to NM_199261.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr21:10920164 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr21:10908854 C>T maps to NM_199261.2 W497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr21:10933879 G>A maps to NM_199261.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr13:20041438 G>T maps to NM_199254.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr13:20039687 G>A maps to NM_199254.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr13:20012234 G>T maps to NM_199254.2 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr13:20012282 C>T maps to NM_199254.2 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr13:20048103 A>G maps to NM_199254.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr13:20012252 G>A maps to NM_199254.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr20:30365344 C>T maps to ENST00000340513 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr22:50635683 G>C maps to NM_025204.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr9:139814837 G>A maps to ENST00000359662 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr9:139815554 C>T maps to ENST00000359662 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr14:103369713 G>A maps to NM_145725.2 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SW-01A-11D-A42E-08 chr14:103336771 G>A maps to NM_145725.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr2:239234476 C>T maps to NM_015650.3 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr6:111901574 G>A maps to ENST00000340026 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr6:111912577 G>A maps to ENST00000340026 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr6:111896844 C>A did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr6:111913237 G>A maps to ENST00000340026 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr6:111887763 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr1:209936212 C>T maps to NM_025228.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr1:209933677 C>G maps to NM_025228.2 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:27076070 C>T maps to NM_004295.3 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr17:27071270 C>G maps to NM_004295.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr1:211529791 T>A maps to ENST00000427925 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr11:36512194 C>T maps to NM_145803.1 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:2215899 C>T maps to NM_032271.2 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr16:2222351 C>T maps to NM_032271.2 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47S-01A-11D-A23U-08 chr12:112572631 T>C maps to NM_006700.2 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:112585912 C>T maps to NM_006700.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr12:112578768 G>T maps to NM_006700.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr3:49867473 C>T maps to NM_005879.2 K355K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr3:49867148 C>T maps to NM_005879.2 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:49893847 G>A maps to NM_005879.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr3:42243996 G>T maps to NM_001042646.1 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr3:42166927 C>T maps to NM_001042646.1 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:42226216 C>A maps to NM_001042646.1 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:42226283 C>T maps to NM_001042646.1 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:42234640 G>T maps to NM_001042646.1 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr2:202245817 G>A maps to NM_015049.2 S731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:202272279 C>A maps to NM_015049.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr8:71510490 C>T did not map to a codon.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr8:71508502 C>G maps to NM_014294.5 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr8:71520341 C>A maps to NM_014294.5 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:118006500 C>A maps to NM_152402.2 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr4:118005595 G>A maps to NM_152402.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:36872832 G>C maps to NM_014831.2 V2703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr3:36872484 T>C maps to NM_014831.2 V2819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:36897242 C>A maps to NM_014831.2 E1280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:36874734 G>T maps to NM_014831.2 C2069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr3:36873093 G>T maps to NM_014831.2 V2616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:36899291 G>A maps to NM_014831.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:36897516 G>A maps to NM_014831.2 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:36880168 C>T maps to NM_014831.2 E1729E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr3:36898548 G>C maps to NM_014831.2 L844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr3:36873953 T>G maps to NM_014831.2 R2330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr16:3739138 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:3740849 G>A maps to NM_016292.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:7834867 G>C maps to NM_001166621.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr21:45518305 C>G maps to NM_003274.4 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr21:45522806 C>T maps to NM_003274.4 F1165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr21:45503017 G>C maps to NM_003274.4 T691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr21:45503078 C>T maps to NM_003274.4 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr21:45496467 G>T maps to NM_003274.4 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr21:45497581 C>T maps to NM_003274.4 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr21:45499916 C>G maps to NM_003274.4 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr21:45479021 C>T maps to NM_003274.4 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr21:45518369 C>T maps to NM_003274.4 L1101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr16:88923572 C>T maps to NM_016209.3 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:45681424 G>A maps to NM_024108.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr14:39627490 G>A maps to NM_001079537.1 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr8:140922486 C>T maps to NM_031466.5 E1054E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr3:108568094 T>A maps to NM_016388.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr10:17191110 C>T maps to NM_004412.5 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr6:123892117 G>C maps to NM_006073.2 S61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:118529681 G>A maps to ENST00000264029 Q493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr11:118529629 G>T maps to ENST00000264029 S510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr6:41126513 C>T maps to NM_018965.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:41121534 G>A maps to NM_178174.2 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr6:41162314 C>G maps to ENST00000373108 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr6:41166030 C>T maps to ENST00000373108 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:41160554 C>T maps to ENST00000373108 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr6:41196515 C>G maps to NM_198153.2 S43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr6:42236136 G>A maps to NM_033502.2 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr6:42237183 G>A maps to NM_033502.2 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:42235917 G>A maps to NM_033502.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr6:42224507 T>C maps to NM_033502.2 E846E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr6:42227197 C>T maps to NM_033502.2 P716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr6:42222654 C>A maps to NM_033502.2 E864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr6:42236620 G>A maps to NM_033502.2 Y236Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr3:48508314 G>C maps to NM_016381.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:152710200 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr12:72667109 T>C maps to NM_013381.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr12:72680476 C>T maps to NM_013381.2 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:72666767 G>C maps to NM_013381.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr12:72666920 G>T maps to NM_013381.2 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:72666689 C>T maps to NM_013381.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr12:73012709 C>T maps to NM_013381.2 I742I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr12:72667205 C>G maps to NM_013381.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr8:110100397 C>T maps to NM_003301.4 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr8:110100121 C>T maps to NM_003301.4 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr8:110131362 C>T maps to NM_003301.4 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr8:126448616 C>T maps to NM_025195.2 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:126448547 C>G maps to NM_025195.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr2:12863642 C>T maps to NM_021643.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:12880799 C>T maps to NM_021643.3 D304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr2:12880460 C>T maps to NM_021643.3 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr2:12858570 G>A maps to NM_021643.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr6:30121746 C>G maps to NM_006778.3 *482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:30128417 C>T maps to NM_006778.3 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr6:30128254 G>A maps to NM_006778.3 H127H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:228582711 C>T maps to NM_145214.2 E367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr1:228589811 C>T maps to NM_145214.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:228588853 G>A maps to NM_145214.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:228594193 G>A maps to NM_145214.2 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr13:50587215 C>T maps to NM_001007278.1 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:100862211 C>T did not map to a codon.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr9:100862389 T>C maps to NM_033219.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:30131830 C>T maps to NM_033229.2 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr17:15532387 G>A maps to ENST00000455584 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:15532171 C>T maps to NM_006470.3 E484E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:15532043 G>C maps to NM_006470.3 S527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr1:228596063 G>A maps to NM_016102.3 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:228602725 G>A maps to NM_016102.3 C16C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr4:154215531 C>T maps to NM_015271.3 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:154245281 C>T maps to NM_015271.3 F668F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:154243968 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:154216910 C>T maps to NM_015271.3 N411N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:5717803 C>A maps to NM_006074.4 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:64890415 C>A maps to NM_001656.3 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr5:64892899 G>A maps to NM_001656.3 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr7:138189077 G>A maps to NM_015905.2 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr7:138255723 T>C maps to NM_015905.2 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr17:54990863 C>G maps to NM_005082.4 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:54991172 C>T maps to NM_005082.4 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:54981705 C>T maps to NM_005082.4 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr17:54978834 G>C maps to NM_005082.4 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr6:30153742 G>A maps to NM_003449.3 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr6:28891283 G>A maps to NM_006510.4 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr6:28872290 G>A maps to NM_006510.4 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr6:28875039 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr6:28889710 C>T maps to NM_006510.4 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr19:59057193 C>T maps to NM_005762.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr19:59059180 C>T maps to NM_005762.2 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:120008355 G>C maps to NM_012101.3 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:30080561 C>T maps to NM_007028.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr9:119461343 G>A maps to NM_012210.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr9:119460353 C>T maps to NM_012210.3 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr1:114970426 G>A maps to NM_015906.3 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr1:114969901 C>T maps to NM_015906.3 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:115006169 A>C maps to NM_015906.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:5655896 G>T maps to NM_001003819.3 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr8:27151742 G>A maps to NM_171982.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr8:27145408 G>A maps to NM_171982.3 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr5:114466548 A>G maps to NM_018700.3 N524N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:57089712 C>A maps to NM_015294.3 G891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr17:57157118 C>T maps to NM_015294.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr17:57076820 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr6:25972266 C>T maps to NM_006355.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr6:25967106 A>G maps to NM_006355.2 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr6:25972224 G>A maps to NM_006355.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:25983671 C>A maps to NM_006355.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr7:99490166 A>G maps to NM_033017.3 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:180660708 C>T maps to NM_033549.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr5:180661585 G>A maps to NM_033549.3 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr5:180659708 G>C maps to NM_033549.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:180661492 C>A maps to NM_033549.3 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr5:180661765 C>G maps to NM_033549.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr5:180661961 C>T maps to NM_201627.1 Q500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr3:140407314 C>T maps to NM_152616.4 N597N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr3:140409904 C>T maps to NM_152616.4 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr3:140401939 C>T maps to NM_152616.4 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr3:140419752 G>A maps to NM_152616.4 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr3:140401603 C>A maps to NM_152616.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr3:140401615 C>A maps to NM_152616.4 Y218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:140397168 C>G maps to NM_152616.4 S33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr3:140407236 C>G maps to NM_152616.4 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:117663655 C>T maps to NM_025188.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr1:155149753 G>A maps to NM_025058.3 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr1:155154487 C>T maps to NM_025058.3 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr7:72738497 G>C maps to NM_178125.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr5:180687502 G>C maps to NM_032765.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr2:27505676 C>T maps to NM_032546.3 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr8:67047318 C>T maps to NM_184085.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr8:67040612 T>C maps to NM_184085.1 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr8:67049349 C>T maps to NM_184085.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr7:100732227 G>A maps to NM_030961.1 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr7:100732140 C>T maps to NM_030961.1 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr7:100731303 G>A maps to NM_030961.1 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:100730634 G>A maps to NM_030961.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:100732689 C>T maps to NM_030961.1 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:248039262 C>T maps to NM_015431.3 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:248028104 G>A maps to NM_015431.3 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr1:248039322 A>G maps to NM_015431.3 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:248020676 C>T maps to NM_015431.3 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:160156856 G>A maps to ENST00000483754 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:160156350 G>A maps to ENST00000483754 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:160155933 G>A maps to NM_173084.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr11:5626755 C>T maps to NM_001003819.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:5624475 G>A maps to NM_001003819.3 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:5624859 C>G maps to NM_001003819.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr4:165962175 C>T maps to NM_152620.2 R318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr4:165962442 C>T maps to NM_152620.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:33613175 C>A maps to NM_018207.2 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:33613110 G>A maps to NM_018207.2 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:26387812 C>T maps to NM_032588.2 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr1:26385114 C>A did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr1:26384976 G>A maps to NM_032588.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr1:26385054 G>A maps to NM_032588.2 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr17:73892976 G>A maps to NM_173547.2 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr17:73887138 G>C maps to NM_173547.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:231298822 G>A maps to NM_001004342.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:231337117 G>A maps to NM_001004342.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:4626602 C>T maps to NM_018073.5 W44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr11:4621769 C>G maps to NM_018073.5 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:4623474 G>A maps to NM_018073.5 N230N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr15:45047417 C>G maps to NM_182985.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr15:45059618 A>G maps to NM_182985.3 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr5:180625768 G>A maps to NM_203293.1 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr3:32927520 G>A maps to NM_001039111.1 K372K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr3:32933230 C>T maps to NM_001039111.1 S845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr3:32932055 C>T maps to NM_001039111.1 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:32932216 C>A maps to NM_001039111.1 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:32932039 G>A maps to NM_001039111.1 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr3:32915443 G>A maps to NM_001039111.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr3:32932658 C>T maps to NM_001039111.1 R655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:31235661 C>G maps to NM_001008274.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr16:31226445 C>T maps to NM_001008274.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr7:75028276 G>A maps to ENST00000430211 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr7:75028289 G>T maps to ENST00000430211 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr14:51464807 G>A maps to ENST00000338969 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr14:51475821 G>A maps to ENST00000338969 Q428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr14:51446212 A>G maps to ENST00000338969 N735N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr4:189068279 C>G maps to NM_178556.3 Y387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr4:189068456 C>A maps to NM_178556.3 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr4:189026056 C>G maps to ENST00000326754 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr5:14358312 G>A maps to NM_007118.2 Q691Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr5:14498738 G>C maps to NM_007118.2 L2774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr5:14336673 G>A maps to NM_007118.2 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr5:14399068 C>T maps to NM_007118.2 R1502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr5:14358453 C>T maps to NM_007118.2 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr5:14291045 G>A maps to NM_007118.2 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:14492920 C>G maps to NM_007118.2 L2626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr5:14406741 C>T maps to NM_007118.2 I1640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr22:38120209 C>T maps to NM_001039141.2 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr22:38121577 C>G maps to NM_001039141.2 T1005T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr22:38164096 G>A maps to NM_001039141.2 K2163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr22:38119891 C>G maps to NM_001039141.2 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr22:38120038 C>G maps to NM_001039141.2 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr22:38150985 G>T maps to NM_001039141.2 E1828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr22:38121881 C>T maps to NM_001039141.2 Q1107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr19:6750314 G>T maps to ENST00000313244 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr19:6741136 G>A did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr14:92466416 T>A maps to NM_004239.3 A1531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr14:92471336 G>A maps to NM_004239.3 Q995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:230656621 G>A maps to ENST00000389044 L1432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr2:230661453 G>A maps to ENST00000389044 V1196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:230636273 G>C maps to ENST00000389044 V1896V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr2:230668933 G>C maps to ENST00000389044 S860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr2:230723894 G>C maps to ENST00000389044 S207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:230673085 C>G did not map to a codon.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr2:230656915 C>A maps to ENST00000389044 E1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr2:230661445 G>C maps to ENST00000389044 S1199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:230662471 A>G maps to ENST00000389044 D1159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr5:908552 G>A maps to NM_004237.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr7:100469280 C>T maps to NM_003302.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr7:100468337 G>A maps to NM_003302.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr1:40349154 G>A maps to ENST00000316891 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:40309839 C>T maps to ENST00000316891 E389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr19:13221039 G>A maps to NM_001136035.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:13218410 G>A maps to NM_001136035.2 F520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:13220476 C>A maps to NM_001136035.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:126320718 G>A maps to NM_001031712.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr6:126342383 A>T maps to NM_001031712.2 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr6:126319270 G>A maps to NM_001031712.2 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr11:64084437 C>T maps to NM_016404.1 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr22:20100674 G>A maps to ENST00000439169 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr22:20102493 G>A maps to ENST00000439169 H333H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr22:20100530 C>A did not map to a codon.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr23:100275517 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr23:100273981 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr23:100276964 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:100296326 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr23:100275491 C>G did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr14:61442400 G>A maps to NM_020810.2 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr20:5927103 C>T maps to NM_015939.3 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:5924672 C>A maps to NM_015939.3 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:29074091 G>A maps to NM_017910.3 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:29084013 G>A maps to NM_017910.3 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:29092606 G>T maps to NM_017910.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:3189209 G>A maps to NM_182916.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:54956579 T>C did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr23:54949136 A>G did not map to a codon.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr23:54955642 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr23:54957053 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr23:54954193 G>A did not map to a codon.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr23:54954189 G>A did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr23:54951478 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:54957732 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:49719323 C>T maps to NM_005480.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr12:49724690 C>G maps to NM_005480.3 S688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:72977733 A>T maps to NM_007332.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr8:72959439 T>C maps to NM_007332.2 V636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr8:72964949 C>T maps to NM_007332.2 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr8:72975701 C>T maps to NM_007332.2 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr8:72951099 C>T maps to NM_007332.2 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr8:72964942 G>A maps to NM_007332.2 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr4:122831315 G>A maps to NM_001130698.1 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:122853554 C>T maps to NM_001130698.1 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr4:122801034 T>A did not map to a codon.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr13:38211240 A>G maps to NM_003306.1 H916H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr13:38320156 G>A maps to NM_003306.1 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:38225497 C>T maps to NM_003306.1 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:38320180 C>A maps to NM_003306.1 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:38357146 G>A maps to NM_003306.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr13:38320373 G>T maps to NM_003306.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr13:38211282 C>T maps to NM_003306.1 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr13:38320316 G>A maps to NM_003306.1 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr20:33609025 G>C maps to NM_015638.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:33632446 G>A maps to NM_015638.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr20:33637719 C>T maps to NM_015638.2 K202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:33591401 G>C maps to NM_015638.2 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:33596492 C>T maps to NM_015638.2 K523K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr23:111095601 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:111019658 G>A did not map to a codon.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr23:111155556 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr23:111090495 C>G did not map to a codon.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr23:111019558 T>C did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:111095543 C>T did not map to a codon.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr23:111090394 C>A did not map to a codon.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr23:111090619 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:111020172 T>A did not map to a codon.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr23:111155827 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr23:111019792 T>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:111019634 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr11:101359739 G>A maps to NM_004621.5 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr11:101362285 C>G did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr11:101342891 G>A maps to NM_004621.5 I727I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr5:135549200 C>G maps to NM_020389.2 L837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:135549149 C>T maps to NM_020389.2 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr5:135693044 G>A maps to NM_020389.2 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr15:31358300 G>A maps to NM_002420.4 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:31360133 G>A maps to NM_002420.4 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr15:31332491 C>T maps to NM_002420.4 Q693Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr15:31354886 G>A maps to NM_002420.4 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr15:31324990 C>A maps to NM_002420.4 V929V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr15:31294287 G>A maps to NM_002420.4 R1517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr15:31327778 G>A maps to NM_002420.4 I868I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr15:31320533 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr15:31340142 C>T did not map to a codon.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr21:45861639 C>G maps to ENST00000397932 L1534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:45811153 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr21:45861675 C>T maps to ENST00000397932 A1546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr21:45837923 C>T maps to ENST00000397932 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr21:45786734 C>T maps to ENST00000397932 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr21:45789213 G>C maps to ENST00000397932 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr21:45844772 G>A maps to ENST00000397932 R1246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr21:45799046 C>T maps to ENST00000397932 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr9:73233872 G>A maps to ENST00000419692 H710H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr9:73235172 C>A maps to ENST00000419692 E604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr9:73478028 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr9:73213433 G>T maps to ENST00000419692 V937V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr19:49674872 C>T maps to NM_017636.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr19:49713573 C>T maps to NM_017636.3 I1080I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:49692257 C>G maps to NM_017636.3 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:49661513 G>A maps to NM_017636.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:2432684 C>G maps to ENST00000452833 A895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:2436596 C>T maps to ENST00000452833 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:2432723 C>A maps to ENST00000452833 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr11:2428415 G>A maps to ENST00000452833 L1019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr9:77448961 G>A maps to NM_017662.4 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:77416816 G>C maps to NM_017662.4 S669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr9:77397393 T>A did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr9:77400852 C>T maps to NM_017662.4 R952R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr9:77377182 G>A maps to NM_017662.4 I1468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:77365632 G>C maps to NM_017662.4 L1668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr9:77386740 G>T maps to NM_017662.4 L1138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr9:77415293 G>T maps to NM_017662.4 S705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr15:50888504 G>C maps to NM_017672.4 V1079V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr15:50911947 G>C maps to NM_017672.4 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:50867259 G>T maps to NM_017672.4 S1603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr2:234923249 C>T maps to NM_024080.4 I1103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr2:234879063 G>C maps to NM_024080.4 V783V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr2:234878871 G>A maps to NM_024080.4 K719K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:234905160 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr8:116599539 C>T maps to NM_014112.2 E796E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr8:116599371 C>A maps to NM_014112.2 A852A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr8:116631649 C>A maps to NM_014112.2 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr8:116599776 A>T maps to NM_014112.2 T717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr8:116430557 C>T maps to NM_014112.2 S941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr8:116631649 C>T maps to NM_014112.2 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr8:116599643 G>A maps to NM_014112.2 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr8:116632045 C>G maps to NM_014112.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr17:3494636 G>A maps to ENST00000399756 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr17:3475543 C>T did not map to a codon.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr17:3495467 G>A maps to ENST00000399756 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:3491561 G>A maps to ENST00000399756 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr17:16330067 G>A maps to NM_016113.4 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr17:16327059 C>T maps to NM_016113.4 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr17:16321005 A>T maps to NM_016113.4 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:3458045 C>T maps to ENST00000381913 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr17:3445954 C>G maps to ENST00000381913 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr17:3432258 G>A maps to ENST00000381913 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr17:3438936 G>A maps to ENST00000381913 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr12:110230225 G>A maps to NM_021625.4 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr12:110238504 G>A maps to NM_021625.4 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr12:110230174 G>A maps to NM_021625.4 Y628Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr12:110226306 G>A maps to NM_021625.4 Y702Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr12:110230582 G>C maps to NM_021625.4 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:110236472 G>A maps to NM_021625.4 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr7:142626152 C>A maps to NM_019841.4 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr7:142627452 G>A maps to NM_019841.4 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr7:142605799 C>T maps to NM_019841.4 R690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:142612711 G>A maps to NM_019841.4 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:142571844 G>A maps to NM_018646.2 I501I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr7:142574199 G>C maps to NM_018646.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr7:142574307 G>C maps to NM_018646.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr7:142569513 A>T maps to NM_018646.2 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:98528284 C>T maps to ENST00000359863 I1141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr7:98563391 G>A maps to ENST00000359863 R2343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr7:98547452 G>A maps to ENST00000359863 L1701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr7:98507926 G>A maps to ENST00000359863 K533K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:98534848 G>A maps to ENST00000359863 L1394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:98533268 C>G maps to ENST00000359863 S1361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:116734975 A>T maps to NM_139169.4 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr10:116732025 C>T maps to NM_139169.4 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr9:131073220 C>A maps to NM_015679.1 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr9:135781385 G>A maps to NM_000368.4 Q527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr9:135781404 G>A maps to NM_000368.4 H520H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr9:135797313 G>C maps to NM_000368.4 Y185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr9:135782757 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr9:135781357 A>T maps to NM_000368.4 L536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:135786886 G>A maps to NM_000368.4 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FH-01A-11D-A38G-08 chr9:135772831 C>A maps to NM_000368.4 E931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:135781418 G>A maps to NM_000368.4 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr9:135781235 C>A maps to NM_000368.4 E577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr9:135802691 C>A did not map to a codon.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr9:135776219 G>C maps to NM_000368.4 S836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr9:135782757 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:135776114 G>C maps to NM_000368.4 S871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr9:135778174 C>G did not map to a codon.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr9:135798754 G>T maps to NM_000368.4 S163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr9:135786886 G>A maps to NM_000368.4 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr9:135777086 C>A did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr9:135801021 A>G maps to NM_000368.4 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr9:135804160 G>T maps to NM_000368.4 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr9:135772844 C>T maps to NM_000368.4 Q926Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr9:135779171 G>A maps to NM_000368.4 R692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr9:135772891 C>A maps to NM_000368.4 E911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr16:2098702 G>A maps to NM_000548.3 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr16:2121803 G>T maps to NM_000548.3 E656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr16:2136339 C>T maps to NM_000548.3 D1603D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr16:2130276 C>A maps to NM_000548.3 S1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr16:2098648 G>A maps to NM_000548.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr16:2129297 C>T maps to NM_000548.3 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:2115599 G>A maps to NM_000548.3 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr16:2138121 G>A maps to NM_000548.3 Q1714Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr16:2129414 C>T maps to NM_000548.3 S1090S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:2110795 G>A maps to NM_000548.3 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr16:2124382 C>T maps to NM_000548.3 F846F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr16:2131629 G>A maps to NM_000548.3 P1215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr13:45147766 G>C maps to NM_183422.2 S815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:45147905 G>A maps to NM_183422.2 Q769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:45149589 C>T maps to NM_183422.2 Q207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr13:45010653 C>T maps to NM_006022.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr13:45148764 C>T maps to NM_183422.2 E482E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr3:150127593 C>T maps to NM_014779.2 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr3:150127841 G>T maps to NM_014779.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:150140898 C>G maps to NM_014779.2 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr3:150176289 C>G maps to NM_014779.2 S737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:107018394 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:106957958 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr7:100064707 C>T maps to NM_030935.3 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr7:100064707 C>T maps to NM_030935.3 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr3:12560568 G>A maps to NM_025265.3 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr3:12545186 C>T maps to NM_025265.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:54695739 G>T maps to NM_001077446.2 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr17:73512920 C>T maps to NM_207346.2 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr17:73515089 G>A maps to NM_207346.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:58177059 C>G maps to NM_001172696.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr11:18503373 C>A maps to NM_006292.2 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr11:18502152 G>A maps to NM_006292.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr2:99722091 C>T maps to NM_025244.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr11:65713199 G>A maps to NM_152762.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr11:65714976 G>A maps to NM_152762.2 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr7:130353956 G>T maps to NM_052933.2 S242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:130357608 C>T maps to NM_052933.2 S165S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CF-A9FL-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr7:130044469 C>A maps to NM_018718.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr14:81606085 G>C maps to NM_000369.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr18:72999587 C>T maps to NM_005786.4 F697F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr18:72999152 G>A maps to NM_005786.4 Q552Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:72999404 G>A maps to NM_005786.4 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr18:72999302 G>A maps to NM_005786.4 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:51871959 G>T maps to NM_173485.5 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr20:51871953 G>T maps to NM_173485.5 E653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr20:51872072 C>T maps to NM_173485.5 I692I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr20:51872204 C>T maps to NM_173485.5 V736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr20:51872503 C>A maps to NM_173485.5 S836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:51870953 G>A maps to NM_173485.5 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr20:51871673 T>A maps to NM_173485.5 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr20:51871205 T>C maps to NM_173485.5 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr19:31768736 G>A maps to NM_020856.2 I654I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:31768940 C>T maps to NM_020856.2 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr19:31770236 A>G maps to NM_020856.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:31768676 C>T maps to NM_020856.2 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr19:31769042 G>A maps to NM_020856.2 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:31768031 C>T maps to NM_020856.2 Q889Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr19:31768367 G>A maps to NM_020856.2 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr19:31769795 T>C maps to NM_020856.2 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr19:31769711 C>T maps to NM_020856.2 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr19:31770002 G>A maps to NM_020856.2 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr19:31769549 C>T maps to NM_020856.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr19:31768817 C>T maps to NM_020856.2 K627K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:50248468 G>A maps to NM_021733.1 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr11:76506761 C>T maps to NM_015516.3 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr11:76507493 G>A maps to NM_015516.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr5:110407680 C>T maps to NM_033035.4 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr2:122513375 C>T maps to NM_004622.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr8:143427113 G>A maps to ENST00000445818 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:143396399 G>C maps to ENST00000445818 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr8:143425519 C>A maps to ENST00000445818 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr1:231700377 G>C maps to NM_005999.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr1:46650907 T>C maps to NM_005727.3 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr17:79612040 C>T maps to NM_031945.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr17:79612271 C>T maps to NM_031945.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr12:31132580 C>T maps to NM_001080509.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:31106946 C>T maps to NM_001080509.2 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr7:120446674 G>A maps to NM_012338.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr10:82269118 G>A maps to NM_030927.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr10:82269070 C>A maps to NM_030927.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr10:82269103 C>G maps to NM_030927.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr10:71243547 C>T maps to NM_012339.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr10:71243520 T>C maps to NM_012339.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr10:71264210 C>T maps to NM_012339.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr5:176079892 C>G maps to NM_012171.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr11:44950726 T>C maps to NM_130783.4 *249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:115601536 T>C maps to NM_005725.4 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr1:115600187 A>G maps to NM_005725.4 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr15:77348524 C>A maps to NM_005724.5 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr15:77345241 T>G maps to NM_005724.5 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr15:77348408 G>A maps to NM_005724.5 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr12:58140802 C>A maps to NM_005981.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:58139981 C>G maps to NM_005981.3 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:58140799 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:128802295 C>T maps to NM_178562.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr7:128802277 G>T maps to NM_178562.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr11:862608 C>T maps to ENST00000409531 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:99888411 A>T did not map to a codon.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr23:99888428 C>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr23:38534988 A>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:38525536 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr22:43557147 G>T maps to NM_000714.4 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:41011325 G>C maps to NM_001159726.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr6:41010862 T>C maps to NM_001159726.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr23:53115485 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:53114926 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:53115044 G>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:116575045 C>G maps to ENST00000368611 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr8:98288923 C>T maps to NM_033512.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr2:54482376 G>A maps to NM_001003937.2 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr2:54482250 G>A maps to NM_001003937.2 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr17:2234306 C>T maps to NM_018128.4 Q531Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr23:54470497 C>G did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr23:54470514 C>T did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:112769840 G>A maps to NM_032028.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr5:112769744 G>A maps to NM_032028.3 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr5:112769768 G>A maps to NM_032028.3 D256D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-4Z-AA7M-01A-11D-A391-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr22:19118989 C>A maps to NM_053006.4 V26V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-E7-A7PW-01A-11D-A34U-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:32828366 C>G maps to NM_052841.3 S22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:24677183 G>A maps to NM_001184739.1 Q283Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr14:24677228 C>A maps to NM_001184739.1 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr22:37414344 G>A maps to NM_003312.4 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr22:37414713 G>A maps to NM_003312.4 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr9:100388270 G>T maps to NM_139246.4 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr6:43221098 C>T maps to NM_032538.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:43251282 G>A maps to NM_032538.1 E935E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr6:43223527 G>T maps to NM_032538.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr15:43044919 C>A maps to ENST00000263802 E1247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr15:43109247 G>A maps to ENST00000263802 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr15:43038151 G>A maps to ENST00000263802 P1597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr15:43045157 A>G maps to ENST00000263802 H1167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:113210176 G>C maps to NM_017868.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:113187035 C>T maps to NM_017868.3 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr11:113194053 C>T maps to NM_017868.3 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr11:113215138 C>T maps to NM_017868.3 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr11:113235555 G>C did not map to a codon.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr11:113235701 T>G maps to NM_017868.3 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:231061311 C>G maps to NM_024525.4 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr9:130482602 G>T maps to NM_144965.1 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr9:130488526 G>A maps to NM_144965.1 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr9:130493028 C>A maps to NM_144965.1 S656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr11:43380572 C>T maps to NM_018259.5 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr11:43465052 G>A maps to NM_018259.5 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:43380572 C>T maps to NM_018259.5 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr11:43436142 C>T maps to NM_018259.5 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:75056798 C>T did not map to a codon.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr10:75029410 A>G maps to NM_145170.3 N1066N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr10:75051134 C>T maps to NM_145170.3 Q766Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr10:75107978 G>A maps to NM_145170.3 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr10:75013810 C>A maps to NM_145170.3 L1096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr10:75051148 C>A maps to NM_145170.3 E762*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-A2I4-01A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:15902869 C>G maps to NM_017775.2 S24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr17:15928486 T>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:15928355 C>T maps to NM_017775.2 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr3:39170377 C>T maps to ENST00000301819 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr3:39178762 C>G maps to ENST00000301819 S1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr3:39180206 C>T maps to ENST00000301819 L1298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43U-01A-11D-A23U-08 chr3:39174682 G>T maps to ENST00000301819 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:39162528 C>T maps to ENST00000301819 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:39162591 C>T maps to ENST00000301819 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:166805936 G>A maps to NM_024753.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:55266752 C>T maps to NM_001114108.1 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:55266611 G>A maps to NM_001114108.1 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr15:99696484 C>T maps to NM_022905.4 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:34867122 G>A maps to NM_144725.3 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:34867122 G>A maps to NM_144725.3 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr5:34867122 G>A maps to NM_144725.3 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr5:34850408 G>T maps to NM_144725.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr5:34867122 G>A maps to NM_144725.3 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:40117263 A>G maps to ENST00000377543 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr7:138863035 C>G maps to NM_024926.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr7:138845755 C>T maps to NM_024926.2 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr7:138853112 C>T maps to NM_024926.2 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMJ-01A-11D-A42E-08 chr7:138865895 C>T maps to NM_024926.2 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr2:33012107 G>A maps to NM_017735.4 Q630Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr2:33012170 T>C maps to NM_017735.4 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr4:147741315 C>G maps to ENST00000513335 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr4:147754964 G>A maps to ENST00000513335 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr4:147795907 G>T maps to ENST00000513335 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr4:147796038 G>A maps to ENST00000513335 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr21:38461128 G>A maps to NM_003316.3 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr21:38463618 G>C maps to NM_003316.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr21:38560803 A>G maps to NM_003316.3 V1644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr2:178417115 C>A maps to NM_152517.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr2:178417479 C>G maps to NM_152517.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr2:74717815 G>T maps to NM_022492.4 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr2:74719338 C>T maps to NM_022492.4 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr2:74717851 C>T maps to NM_022492.4 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr2:20101519 G>T maps to NM_001008237.1 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr5:94858954 G>A maps to NM_014639.3 R570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr5:94876438 G>A maps to NM_014639.3 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr5:94878949 G>A maps to NM_014639.3 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr5:94803601 A>G maps to NM_014639.3 L1530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr5:94861309 G>T maps to NM_014639.3 S401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr5:94849304 G>C maps to NM_014639.3 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr22:46664424 G>A maps to NM_017931.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr1:51754578 C>T maps to ENST00000447632 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:51770784 G>A maps to ENST00000447632 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr9:15187021 C>T maps to NM_152574.2 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:15188059 C>T maps to NM_152574.2 W435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr9:15182307 G>A maps to NM_152574.2 Q574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr14:20768969 G>C maps to NM_138376.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr14:20767553 C>T maps to NM_138376.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:47300851 G>A maps to ENST00000394850 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr2:47206028 G>C maps to ENST00000394850 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr2:47301005 G>T maps to ENST00000394850 E865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:91196426 G>A maps to NM_001010854.1 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr14:91252588 G>A maps to NM_001010854.1 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr14:91007864 C>T maps to NM_001010854.1 V793V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:71137850 G>A maps to NM_015351.1 Q216Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr14:71134434 G>C maps to NM_015351.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:40723190 G>A maps to NM_152479.5 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr19:40724186 G>C maps to NM_152479.5 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr11:62496385 G>A maps to NM_173810.3 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr9:135276960 G>A maps to NM_007344.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr9:135275527 C>T maps to NM_007344.2 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr9:135278022 G>A maps to NM_007344.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr9:135278022 G>C maps to NM_007344.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:117633210 G>T maps to NM_003594.3 E852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:117629134 C>G maps to NM_003594.3 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:117618441 C>A maps to NM_003594.3 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:117633951 C>G maps to NM_003594.3 S864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr1:117634535 C>G maps to NM_003594.3 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:117603116 G>A maps to NM_003594.3 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr1:117638918 C>T maps to NM_003594.3 Q1062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr6:80723065 G>T maps to NM_003318.4 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr6:80721189 C>G maps to NM_003318.4 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr6:80747682 G>A did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr22:43459893 C>T maps to NM_012263.4 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr22:43442435 G>A maps to NM_012263.4 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr22:43442528 G>C maps to NM_012263.4 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:43447824 C>T maps to NM_012263.4 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr22:43459908 G>A maps to NM_012263.4 C219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr22:43460229 G>A maps to NM_012263.4 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr9:124751554 C>T maps to NM_001139442.1 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr22:43575732 G>A maps to NM_015140.3 Y244Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr22:43575865 C>G maps to NM_015140.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr15:90796577 C>G maps to ENST00000438251 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr15:90799462 C>T maps to ENST00000438251 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr15:90794784 G>A did not map to a codon.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr6:167755004 G>A maps to NM_031949.4 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:167754886 C>G maps to NM_031949.4 S500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:167754002 G>A maps to NM_031949.4 K205K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr6:167755013 G>C maps to NM_031949.4 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr3:9877037 C>T maps to NM_001025930.3 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr3:9854766 G>A maps to NM_001025930.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:219602554 C>T maps to NM_014640.4 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr2:219611748 C>T maps to NM_014640.4 F666F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr2:219610930 C>T maps to NM_014640.4 R651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr2:219618350 G>C maps to NM_014640.4 V1101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:76249832 C>T maps to NM_015072.4 I982I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:76211451 C>G maps to NM_015072.4 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:76232589 G>T maps to NM_015072.4 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr14:76219286 C>G maps to NM_015072.4 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr17:46862466 C>A maps to NM_001130918.1 E620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:46862407 G>A maps to NM_001130918.1 F639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:84387004 T>G maps to NM_024686.4 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:84412873 C>A maps to NM_024686.4 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr1:84387030 G>A maps to NM_024686.4 Q397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr1:84399295 G>A maps to NM_024686.4 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr22:50470354 G>A maps to NM_001080447.1 H489H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr20:30496505 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr20:30522625 C>T maps to NM_001008409.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr2:179498311 T>C maps to NM_133378.4 V11690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr2:179456847 G>C maps to NM_133378.4 S17360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr2:179640860 C>T maps to NM_133378.4 V1910V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr2:179412923 G>A maps to NM_133378.4 S28575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr2:179429787 G>T maps to NM_133378.4 S24456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr2:179481630 G>T maps to NM_133378.4 T13427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr2:179566788 G>A maps to NM_133378.4 I8928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr2:179604999 G>A maps to NM_133437.3 V4149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr2:179414018 T>A maps to NM_133378.4 T28210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr2:179638745 A>G maps to NM_133378.4 S2383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr2:179641727 G>T maps to NM_133378.4 V1621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr2:179399245 A>G maps to NM_133378.4 Y31464Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr2:179616158 A>C maps to ENST00000375038 T3658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr2:179475789 G>A maps to NM_133378.4 A14454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:179584462 G>C maps to NM_133378.4 S6675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:179422795 A>G maps to NM_133378.4 I26527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:179629029 C>G did not map to a codon.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr2:179596191 G>A maps to NM_133378.4 S4523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr2:179426876 C>A maps to NM_133378.4 V25426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr2:179566961 C>T maps to NM_133378.4 S8904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:179481948 C>A maps to NM_133378.4 E13357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr2:179413247 C>T maps to NM_133378.4 L28467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:179489390 C>T maps to NM_133378.4 L12304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:179433785 A>G maps to NM_133378.4 D23123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr2:179575376 G>A maps to NM_133378.4 Q8239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:179478784 G>A maps to NM_133378.4 Q13879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:179419843 C>A maps to NM_133378.4 E26880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:179421584 G>A maps to NM_133378.4 I26864I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:179435389 G>A maps to NM_133378.4 R22589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:179558366 G>A maps to NM_133378.4 A9277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:179591847 G>A maps to NM_133378.4 S5504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:179593505 C>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:179656914 C>A maps to NM_133378.4 E516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr2:179498206 A>T maps to NM_133378.4 L11725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr2:179478566 T>G maps to NM_133378.4 P13913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr2:179403717 C>A maps to NM_133378.4 E30414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr2:179540672 C>T maps to NM_133378.4 K10203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr2:179584712 G>A maps to NM_133378.4 L6642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:179647611 C>T maps to NM_133378.4 A1007A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:179659275 C>T maps to NM_133378.4 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr2:179631276 G>A maps to NM_133378.4 H3178H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr2:179453643 G>A maps to NM_133378.4 F18368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr2:179629317 G>C maps to NM_133378.4 V3308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr2:179474564 C>T maps to NM_133378.4 K14627K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:179472308 A>C maps to NM_133378.4 P15134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:179398126 G>A maps to NM_133378.4 L31837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr2:179455905 C>A maps to NM_133378.4 L17614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr2:179482789 A>T maps to NM_133378.4 L13195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr2:179539825 T>A maps to NM_133378.4 K10217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr2:179594394 C>T maps to NM_133378.4 V4951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:179399305 G>A maps to NM_133378.4 I31444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:179472970 C>A maps to NM_133378.4 E14979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:179577888 G>C maps to NM_133378.4 S7747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:179591901 G>A maps to NM_133378.4 L5486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:179605086 G>C maps to NM_133437.3 V4120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr2:179392356 G>A maps to NM_133378.4 F33264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr2:179590329 G>A maps to NM_133378.4 A5623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:179471895 C>T maps to NM_133378.4 W15243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr2:179605359 C>T maps to NM_133437.3 E4029E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:179403928 C>T maps to NM_133378.4 K30343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:179617849 C>A did not map to a codon.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr2:179600721 T>C maps to NM_133378.4 T3573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr2:179622542 G>T maps to NM_133432.3 I3422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr2:179444735 G>A maps to NM_133378.4 F19858F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr2:179597383 G>A maps to NM_133378.4 C4224C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr2:179640985 G>A maps to NM_133378.4 Q1869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr2:179497729 G>A maps to NM_133378.4 I11808I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:179587112 A>G maps to NM_133378.4 T6223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:179451490 G>A maps to NM_133378.4 T18811T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:179482572 G>A maps to NM_133378.4 A13267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:179577066 G>T maps to NM_133378.4 S7950S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr2:179404370 G>A maps to NM_133378.4 D30239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr2:179425246 C>A maps to NM_133378.4 E25970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr2:179579809 G>A maps to NM_133378.4 H7457H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr2:179425409 G>A maps to NM_133378.4 I25915I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr2:179428166 C>A maps to NM_133378.4 A24996A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr2:179644784 A>T maps to NM_133378.4 L1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr2:179644786 G>T maps to NM_133378.4 A1223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr2:179411949 G>A maps to NM_133378.4 H28866H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr2:179582432 G>A maps to NM_133378.4 Q7146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:179429552 G>T maps to NM_133378.4 T24534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr2:179474919 G>T maps to NM_133378.4 L14543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr2:179634498 G>A maps to NM_133378.4 Q2937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr2:179442901 G>C maps to NM_133378.4 L20212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:179399172 C>A maps to NM_133378.4 E31489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:179578816 G>C maps to NM_133378.4 T7612T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr2:179457373 C>T maps to NM_133378.4 L17218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr2:179474259 C>T maps to NM_133378.4 V14691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr2:179590530 C>A maps to NM_133378.4 G5596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr2:179641975 G>A maps to NM_133378.4 R1572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr2:179665392 G>A maps to NM_133378.4 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr2:179623720 C>T maps to NM_133378.4 L3431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:179639675 G>A maps to NM_133378.4 V2254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr2:179442545 A>G maps to NM_133378.4 G20301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr2:179464158 A>T maps to NM_133378.4 P16219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr2:179642656 A>G maps to NM_133378.4 S1418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr2:179441725 G>A maps to NM_133378.4 F20544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr2:179553470 C>T maps to NM_133378.4 K9466K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr2:179479480 C>A did not map to a codon.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr2:179482205 G>C maps to NM_133378.4 S13301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr2:179636043 A>G maps to NM_133378.4 D2670D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr2:179440538 G>A maps to NM_133378.4 L20872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:179422474 C>T maps to NM_133378.4 L26634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:179590359 G>A maps to NM_133378.4 V5613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr2:179485017 G>A maps to NM_133378.4 F12842F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:179434503 C>T maps to NM_133378.4 W22884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:179441668 G>A maps to NM_133378.4 V20563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:179546385 A>G did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:179600439 T>A maps to NM_133378.4 V3667V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:179666961 C>A maps to NM_133378.4 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr2:179594421 C>T maps to NM_133378.4 T4942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr2:179451513 T>A maps to NM_133378.4 K18804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:179454354 T>A maps to NM_133378.4 P18131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:179570023 G>C maps to NM_133378.4 L8583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:179641730 A>G maps to NM_133378.4 T1620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr2:179432813 G>A maps to NM_133378.4 V23447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr2:179404285 G>T maps to NM_133378.4 R30268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr2:179431832 C>T maps to NM_133378.4 V23774V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr2:179485544 G>A maps to NM_133378.4 L12696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr2:179590571 G>C maps to NM_133378.4 S5582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:179391762 C>T maps to NM_133378.4 V33416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:179477942 A>G maps to NM_133378.4 A13963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:179466073 G>A maps to NM_133378.4 F15982F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr2:179482767 C>T maps to NM_133378.4 V13202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr2:179574560 G>A maps to NM_133378.4 F8251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr2:179612804 C>T maps to ENST00000375038 K4776K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr2:179417406 C>A maps to NM_133378.4 E27506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr2:179397024 A>G maps to NM_133378.4 L32205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr2:179622548 G>A maps to NM_133432.3 S3420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr2:179641877 G>A maps to NM_133378.4 I1604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr2:179566961 C>A maps to NM_133378.4 S8904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr2:179595718 T>G maps to NM_133378.4 G4647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr2:179425196 G>A maps to NM_133378.4 P25986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr2:179547541 A>G maps to NM_133378.4 Y9748Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:179466259 G>A maps to NM_133378.4 V15920V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:179597027 C>T maps to NM_133378.4 K4312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr2:179600730 G>A maps to NM_133378.4 F3570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr2:179422058 G>A maps to NM_133378.4 F26742F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr2:179621090 C>T maps to NM_133437.3 E3533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr2:179542527 G>A maps to NM_133378.4 L10127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr2:179464413 G>C maps to NM_133378.4 V16170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr2:179429610 G>C maps to NM_133378.4 S24515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr2:179569666 C>T maps to NM_133378.4 E8633E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr8:63998554 G>T maps to NM_000370.3 S9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr8:63976764 C>G maps to NM_000370.3 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:43113070 G>A maps to NM_024331.3 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr20:43118019 A>G maps to NM_024331.3 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr20:43115336 A>T maps to NM_024331.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr18:29178547 C>T maps to ENST00000432547 N156N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:54942275 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr19:54942065 C>T maps to ENST00000391739 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:54937897 C>G maps to ENST00000391739 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr19:54942065 C>T maps to ENST00000391739 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr19:54942065 C>T maps to ENST00000391739 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr17:72233572 C>G maps to NM_032646.5 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:72239551 C>A maps to NM_032646.5 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:72246432 G>A maps to NM_032646.5 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr17:72249947 C>A maps to NM_032646.5 I500I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr17:72248458 C>G maps to NM_032646.5 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr17:72249218 G>C did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:8120356 C>T maps to NM_003320.4 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr12:49523286 G>T maps to NM_006082.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr12:49666206 G>T maps to NM_032704.3 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr13:19751447 G>A maps to NM_006001.1 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr13:19752451 G>A maps to NM_006001.1 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:132238009 G>A maps to NM_080386.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr2:132240419 G>A maps to NM_080386.2 *451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr2:132240252 C>T maps to NM_080386.2 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr2:130951670 C>T maps to NM_207312.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:130951526 G>A maps to NM_207312.2 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr22:18609758 G>A maps to NM_018943.2 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr10:5437319 G>A maps to NM_024803.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr10:5436343 G>C maps to NM_024803.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr6:30691627 C>G maps to NM_178014.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr6:30691513 G>C maps to NM_178014.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr6:30691798 G>A maps to NM_178014.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr6:30692053 G>A maps to NM_178014.2 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr20:57599207 C>T maps to NM_030773.3 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:57598817 G>C maps to NM_030773.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:57599348 C>G maps to NM_030773.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr6:3154783 C>G maps to NM_001069.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr16:90001482 C>T maps to ENST00000304984 Y555Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr16:90002145 G>A maps to ENST00000304984 T776T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr19:6496224 G>A maps to NM_006087.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr19:6496044 G>A maps to NM_006087.2 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr18:12325597 C>T maps to NM_032525.1 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr18:12308768 C>T maps to NM_032525.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr10:95169 C>T maps to NM_177987.2 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr10:94558 G>A maps to NM_177987.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr17:57955629 G>A maps to NM_016261.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr17:57941182 A>C maps to NM_016261.3 Y367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr17:40762123 A>T did not map to a codon.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr17:40767057 G>A maps to NM_001070.4 *452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:40818471 C>G maps to NM_016437.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr17:40818465 C>T maps to NM_016437.2 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr17:40817805 C>T maps to NM_016437.2 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr17:40815490 C>G maps to NM_016437.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr10:135111587 G>A maps to NM_006659.2 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr10:135098626 G>A maps to NM_006659.2 N662N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr10:135103334 G>A maps to NM_006659.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr10:135093395 G>A maps to NM_006659.2 F861F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr10:135098647 G>C maps to NM_006659.2 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr10:135101641 G>A maps to NM_006659.2 D571D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr13:113208460 G>C maps to NM_006322.4 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr13:113200084 G>A maps to NM_006322.4 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr13:113158411 G>A maps to NM_006322.4 I747I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr13:113173333 C>T maps to NM_006322.4 W635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr13:113219480 G>A maps to NM_006322.4 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr15:43695942 G>A maps to ENST00000399460 Q599Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr15:43678470 C>G maps to ENST00000399460 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:43675566 C>G maps to ENST00000399460 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr15:22845768 A>G maps to NM_052903.4 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr15:22867602 C>T maps to NM_052903.4 F893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr15:22872422 A>G maps to NM_052903.4 E984E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr15:22848928 C>T maps to NM_052903.4 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr15:22866949 C>T maps to NM_052903.4 Q823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr15:22840332 A>G maps to NM_052903.4 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr22:50659211 A>G maps to NM_020461.3 S1192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr22:50682165 G>C maps to NM_020461.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr22:50682725 G>A maps to NM_020461.3 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr22:50660231 C>T maps to NM_020461.3 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr22:50658875 T>C maps to NM_020461.3 S1304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr22:50682549 G>A maps to NM_020461.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr22:50682350 G>A maps to NM_020461.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:28857542 G>A maps to NM_003321.4 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr1:151546837 C>T maps to NM_020127.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:35478695 C>G maps to NM_003322.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:35478695 C>G maps to NM_003322.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr6:35466226 G>A maps to NM_003322.3 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr19:49384273 G>A maps to NM_003323.2 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr19:49391422 G>A maps to NM_003323.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr19:49391497 C>T maps to NM_003323.2 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr12:3039494 C>G maps to NM_001160408.1 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr12:3040252 C>T maps to NM_001160408.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr6:158834167 G>A maps to NM_020245.3 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:158735143 G>A maps to NM_020245.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr6:158923364 C>A maps to NM_020245.3 T890T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr6:158922866 G>A maps to NM_020245.3 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr6:158922809 G>A maps to NM_020245.3 Q705Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:158870053 G>A maps to NM_020245.3 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr17:1183552 G>A maps to NM_172367.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr11:62343414 G>A maps to NM_022830.2 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:62358933 G>A maps to NM_022830.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:62348891 G>C maps to NM_022830.2 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr11:62344705 G>C maps to NM_022830.2 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr12:44196142 C>T maps to NM_002822.3 Q110Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr3:52265546 C>G maps to NM_007284.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:52264888 C>T maps to ENST00000494383 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:52263175 G>C maps to NM_007284.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr7:19156467 G>A maps to NM_000474.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr7:19738145 G>A maps to NM_001002926.1 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr18:9396404 C>T maps to NM_020648.5 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:48096181 C>T maps to NM_003328.2 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr4:48078436 G>C maps to NM_003328.2 S407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr4:48106973 T>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:48073623 G>C maps to NM_003328.2 V475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr4:48096192 G>A maps to NM_003328.2 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr4:48114451 C>T maps to NM_003328.2 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr1:32650144 G>A maps to NM_175852.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr1:32660670 G>T maps to NM_175852.3 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:32647029 G>A maps to NM_175852.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr6:139564324 C>A maps to ENST00000358430 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr23:16850771 G>A did not map to a codon.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr23:16846328 C>T did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:16859632 A>G did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:16857986 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:16846366 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:16857973 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:52490247 C>A maps to NM_015913.2 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B0-01A-11D-A31L-08 chr1:52489169 G>T maps to NM_015913.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr5:134235318 C>T maps to NM_024715.3 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr5:134232071 C>T maps to NM_024715.3 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr14:52899096 A>G maps to NM_020784.2 N801N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:52936857 C>T maps to NM_020784.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:52899116 G>A maps to NM_020784.2 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr14:52949609 C>A maps to NM_020784.2 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr14:52899138 G>A maps to NM_020784.2 V787V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr7:37901703 T>C maps to NM_016616.4 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr7:37916592 C>G maps to NM_016616.4 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:7899901 G>A maps to NM_030810.3 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:7886243 G>A maps to NM_030810.3 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:7891865 G>A maps to NM_030810.3 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr6:7891940 C>T maps to NM_030810.3 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr3:138023785 G>A maps to ENST00000333911 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr1:145438894 G>C maps to NM_006472.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr1:145439608 G>C maps to NM_006472.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:145440908 C>G maps to NM_006472.3 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr1:145439042 C>T maps to NM_006472.3 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:145440987 C>T maps to NM_006472.3 Q359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:145440398 A>G maps to NM_006472.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr18:54278229 G>A maps to NM_004786.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr18:77733765 G>A maps to NM_006701.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:104719162 C>T maps to NM_001093771.1 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr22:19868213 C>A maps to NM_006440.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr22:19870907 C>T maps to NM_006440.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr22:19864726 C>T maps to NM_006440.3 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr22:19882960 C>A maps to NM_006440.3 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:126291278 G>A maps to NM_001039783.1 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr19:10475634 G>A maps to NM_003331.4 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:10488944 G>A maps to NM_003331.4 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:10461568 G>A maps to NM_003331.4 L1169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:10476363 C>G maps to NM_003331.4 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:10478978 G>A maps to NM_003331.4 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:10488944 G>A maps to NM_003331.4 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr19:10477208 C>T maps to NM_003331.4 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr19:10477148 G>C maps to NM_003331.4 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr19:10461510 C>T maps to NM_003331.4 *1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr19:10476223 C>T maps to NM_003331.4 W327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr19:10476530 G>A maps to NM_003331.4 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr18:672882 C>T maps to NM_001071.2 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr18:670746 G>A maps to NM_001071.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr11:88911795 G>A maps to NM_000372.4 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr11:89028452 G>A maps to NM_000372.4 K503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:88911262 C>T maps to NM_000372.4 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr15:41853505 C>G maps to NM_006293.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr15:41864734 C>T maps to NM_006293.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr15:41860466 C>T maps to NM_006293.3 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr10:71905216 G>T maps to NM_173555.2 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr10:71905919 C>A maps to NM_173555.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr7:66479464 C>T maps to NM_018264.2 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:66482976 C>T maps to NM_018264.2 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr7:72093913 C>T maps to NM_001145440.1 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr7:72285990 C>A maps to NM_001145440.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr7:72081773 A>G maps to NM_001145440.1 H556H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr7:72193852 G>A maps to NM_001145440.1 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr7:72040575 G>A maps to NM_001145440.1 H638H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr7:72081773 A>G maps to NM_001145440.1 H556H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:75198987 C>T maps to NM_138467.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr21:44521542 C>T did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:56175099 C>G maps to NM_007279.2 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr19:56172437 C>T maps to NM_007279.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr19:56179915 C>T maps to NM_007279.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr19:56171956 C>T maps to NM_007279.2 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr15:70961770 G>A maps to NM_018003.2 Q418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr15:70979930 G>A maps to NM_018003.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr15:70961666 G>A maps to NM_018003.2 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr15:70994233 A>C maps to NM_001008224.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:162535884 G>A maps to ENST00000367925 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:162549314 C>T maps to ENST00000367925 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr1:162549265 C>T maps to ENST00000367925 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr9:139975311 C>G maps to NM_207309.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr23:47062395 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:34919420 C>T maps to NM_005499.2 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr19:34949726 A>G maps to NM_005499.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr19:34942883 A>C did not map to a codon.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr19:34942934 G>A maps to NM_005499.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr3:69126978 G>A maps to NM_003968.3 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:69113225 G>A maps to NM_003968.3 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:132390937 T>C maps to NM_024818.3 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr19:18684148 C>T maps to NM_003333.3 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:18684187 C>G maps to NM_003333.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:18684537 C>G maps to NM_003333.3 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr4:68514896 G>A maps to NM_018227.5 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr4:68539450 G>A maps to NM_018227.5 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr4:68539450 G>A maps to NM_018227.5 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr3:49845267 C>T maps to NM_003335.2 V872V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr9:138847183 C>T maps to NM_016172.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr13:100037587 G>A maps to NM_001144072.1 *345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr9:34249793 C>T maps to NM_001171201.1 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:33948388 G>T maps to NM_018449.2 S418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr9:33943440 G>A maps to NM_018449.2 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:154229705 G>A maps to NM_014847.3 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr1:154209610 G>A maps to NM_014847.3 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr1:154228193 C>A maps to NM_014847.3 S707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:154228193 C>G maps to NM_014847.3 S707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:154234111 G>A maps to NM_014847.3 V947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr21:43867302 G>T maps to NM_018961.2 *662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr21:43867193 G>T maps to NM_018961.2 E626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr21:43838514 G>A maps to NM_018961.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:122647791 C>T maps to NM_032873.4 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN4-01A-11D-A42E-08 chr11:122659875 C>T maps to NM_032873.4 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr17:16285490 C>T maps to NM_018955.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr17:16285577 C>A maps to NM_018955.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr17:16285559 T>C maps to NM_018955.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr17:16285559 T>C maps to NM_018955.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SH-01A-11D-A391-08 chr17:16285559 T>C maps to NM_018955.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:16285352 C>T maps to NM_018955.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr12:125397099 G>C maps to NM_021009.5 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr12:125396364 C>T maps to NM_021009.5 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:125398074 C>T maps to NM_021009.5 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr12:125396469 C>T maps to NM_021009.5 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr12:125397651 T>C maps to NM_021009.5 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr6:29523935 G>T maps to NM_006398.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr6:29523822 G>C maps to NM_006398.3 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr23:118708894 G>A did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr23:118708870 G>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr20:44442090 G>A maps to NM_007019.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr20:44442073 A>G did not map to a codon.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr4:103747656 C>T maps to NM_181890.1 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr7:43982599 T>C maps to NM_015983.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:4200036 G>A maps to NM_003342.4 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:1203255 C>T maps to NM_194315.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr22:21965298 G>T maps to ENST00000458578 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr11:57319863 G>A maps to NM_004223.3 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr11:57322054 G>A maps to NM_004223.3 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr19:59068510 C>T maps to NM_003969.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr19:59069643 C>T maps to NM_003969.3 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr19:59067688 G>C maps to NM_003969.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr19:59068070 G>C maps to NM_003969.3 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr23:142967426 A>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:142967293 A>G did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:74387281 G>A maps to NM_022066.3 G1207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr17:74388107 G>A maps to NM_022066.3 I1011I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:74387650 G>A maps to NM_022066.3 F1084F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr17:74387188 T>C maps to NM_022066.3 R1238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:154527950 G>A maps to NM_017582.6 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:154524586 T>C maps to NM_017582.6 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:33886925 C>T maps to NM_017811.3 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:55912935 G>A maps to NM_014501.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr19:55918210 G>T maps to NM_014501.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:55918273 C>A maps to NM_014501.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:55918273 C>T maps to NM_014501.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr1:64680523 G>A maps to ENST00000371077 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:48732031 A>G maps to NM_021988.4 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr8:48955642 C>T maps to NM_003350.2 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr15:25616709 G>C maps to NM_000462.2 S207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr12:109959262 G>A maps to NM_183415.1 E757E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:109945372 C>G maps to NM_183415.1 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr12:109927778 C>G maps to NM_183415.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr12:109937444 C>G maps to NM_183415.1 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr12:109939196 G>A maps to NM_183415.1 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr12:109921379 G>A maps to NM_183415.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr7:157023792 G>A maps to NM_014671.2 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr7:157023792 G>T maps to NM_014671.2 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr7:157000604 G>A maps to NM_014671.2 Q595Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr11:118245801 G>C maps to NM_004788.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr11:118245785 C>G maps to NM_004788.2 S438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:10186931 C>G maps to NM_001105562.2 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:10166290 C>T maps to NM_001105562.2 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr1:10166512 C>T maps to NM_001105562.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr1:10166257 C>G maps to NM_001105562.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:10239489 C>G maps to NM_001105562.2 T1239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr1:10207130 G>A maps to NM_001105562.2 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr1:10197128 C>T maps to NM_001105562.2 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:10132130 C>T maps to NM_001105562.2 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:10190616 G>T maps to NM_001105562.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:10231365 G>A maps to NM_001105562.2 A1168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:11333644 C>T maps to NM_013319.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:11345734 C>T maps to NM_013319.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr1:11333719 G>A maps to NM_013319.2 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr13:30346272 G>A maps to NM_007106.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr23:153714225 C>T did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr23:153713942 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr23:153714158 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr23:153713946 G>C did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr23:153714278 G>C did not map to a codon.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr23:153714207 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:153714141 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:74749004 G>T maps to NM_201265.1 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr5:158710290 C>T maps to NM_145049.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr5:158696066 C>G maps to NM_145049.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:4924306 G>C maps to NM_016936.3 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr16:4903130 C>T maps to NM_016936.3 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr16:4908645 C>T maps to NM_016936.3 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr16:4924864 G>A maps to NM_016936.3 T818T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr7:138958775 G>A maps to NM_173569.3 E643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr7:138966755 G>C maps to NM_173569.3 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:138978024 C>T maps to NM_173569.3 L1239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:138978696 C>T maps to NM_173569.3 L1322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:33458291 C>G maps to NM_001128161.1 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr3:33458306 C>A maps to NM_001128161.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr9:86284122 G>A maps to NM_013438.4 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr9:86281339 C>A maps to NM_013438.4 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr9:86292876 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr9:86284242 C>G did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:56591245 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr23:56590881 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr23:56590916 T>C did not map to a codon.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr23:56591909 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr23:56591563 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr23:56590552 G>C did not map to a codon.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr23:56590640 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:56591016 T>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr23:56590813 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:5530515 G>A maps to NM_017481.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr1:156020907 G>A maps to NM_020131.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:156013834 C>T maps to NM_020131.3 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr11:5537101 G>A maps to NM_145053.4 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr11:5537401 G>A maps to NM_145053.4 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:5537229 G>A maps to NM_145053.4 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr15:43339378 G>A maps to NM_174916.2 Q550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr15:43339471 G>A maps to NM_174916.2 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:43294804 G>A maps to NM_174916.2 L1203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr15:43317140 G>A maps to NM_174916.2 F875F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr15:43313565 T>C maps to NM_174916.2 G949G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr15:43328426 C>T maps to NM_174916.2 Q713Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:43330393 G>C maps to NM_174916.2 S629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr15:43328410 C>A maps to NM_174916.2 E719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr6:42647460 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:42532120 G>T maps to NM_015255.2 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr6:42625825 T>G maps to NM_015255.2 A979A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr6:42637865 G>A maps to NM_015255.2 T1306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:42655959 G>A maps to NM_015255.2 P1620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr6:42600450 C>G maps to NM_015255.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr6:42658906 T>A maps to NM_015255.2 L1755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:42643843 G>A maps to NM_015255.2 G1434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr6:42571354 G>A maps to NM_015255.2 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr6:42658808 G>A maps to NM_015255.2 K1722K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:42541689 T>A maps to NM_015255.2 C99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr2:170917626 G>A maps to ENST00000442603 L1637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:170871818 C>T maps to ENST00000442603 R1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:19441917 C>T maps to ENST00000375267 E3679E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:19449356 G>C maps to ENST00000375267 S3262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:19454158 G>A maps to ENST00000375267 F3062F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:19473458 G>A maps to ENST00000375267 L2555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:19487578 C>T maps to ENST00000375267 Q1746Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4XJ-01A-11D-A26M-08 chr1:19513091 G>A maps to ENST00000375267 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr1:19447815 C>T maps to ENST00000375267 L3336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr1:19420618 C>T maps to ENST00000375267 L4587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:19439181 G>A maps to ENST00000375267 V3879V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr1:19491417 C>T maps to ENST00000375267 V1462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:19441310 C>T maps to ENST00000375267 R3732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:19447914 G>A maps to ENST00000375267 F3303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:19524273 C>T maps to ENST00000375267 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:19525422 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:19511655 G>A maps to ENST00000375267 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr8:103323974 G>A maps to NM_015902.4 F802F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr8:103301749 G>T maps to NM_015902.4 I1548I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:103341573 G>A maps to NM_015902.4 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr8:103266529 C>G maps to NM_015902.4 *2800Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr8:103311098 A>G maps to NM_015902.4 Y1101Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr8:103324467 G>C maps to NM_015902.4 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr8:103291095 C>T maps to NM_015902.4 G2082G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr8:103324049 T>C maps to NM_015902.4 K777K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr8:103284976 G>A maps to NM_015902.4 L2251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr8:103293698 T>A maps to NM_015902.4 G1915G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr14:93693380 G>C maps to NM_175748.3 *426Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr10:99327761 C>T maps to NM_024954.3 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:42289311 G>C maps to NM_014233.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:42290268 G>T maps to NM_014233.2 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr17:42295582 G>A maps to NM_014233.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr11:62444393 G>A maps to NM_015853.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr11:62444339 G>A maps to NM_015853.3 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr1:26610894 G>A maps to NM_183008.2 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr1:26609155 G>A maps to NM_183008.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr8:59358621 A>G maps to NM_001077619.1 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr2:136519443 C>T maps to NM_014607.3 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr19:4447593 C>A maps to NM_025241.2 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:4446588 G>C maps to NM_025241.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:4453978 C>T maps to NM_025241.2 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr3:196089366 C>T maps to NM_015562.1 E342E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr8:30620853 C>T maps to ENST00000265616 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr8:30612198 G>A maps to ENST00000265616 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr4:41263745 C>T maps to NM_004181.4 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr13:76124113 C>T maps to NM_006002.3 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:193020926 C>A maps to ENST00000367450 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:193028360 G>A maps to ENST00000367450 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr9:134405893 G>A maps to NM_031432.2 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr9:134405927 C>T maps to NM_031432.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr1:165859511 C>T maps to NM_012474.4 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr1:165865489 C>T maps to NM_012474.4 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:165860505 C>T maps to NM_012474.4 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:165875180 C>T maps to NM_012474.4 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:62571632 G>A maps to NM_017859.3 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr20:62572545 C>T maps to NM_017859.3 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:5415748 C>T maps to NM_053049.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr4:141489010 G>A maps to NM_021833.4 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:73686630 C>T maps to NM_003355.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:73718075 C>T maps to NM_003356.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:18586471 G>A maps to NM_001040697.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr1:161128199 A>T did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr22:19459218 G>C maps to ENST00000399525 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr22:19462609 G>A maps to ENST00000399525 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr7:100486856 C>T maps to NM_001015072.3 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr4:186329121 C>T maps to NM_018359.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr4:39512008 G>C maps to NM_003359.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr4:39506908 C>T maps to NM_003359.3 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr2:128938564 C>T maps to NM_020120.3 I1334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr2:128880799 G>T maps to NM_020120.3 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr2:128896401 T>C maps to NM_020120.3 Y565Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:128913069 C>T maps to NM_020120.3 F715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr2:128934438 C>A maps to NM_020120.3 L1197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr2:128855036 C>T maps to NM_020120.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr2:128903399 G>A maps to NM_020120.3 Q625Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr13:96506723 C>A maps to NM_020121.3 V1338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr13:96665586 G>A maps to NM_020121.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr13:96505889 G>C maps to NM_020121.3 L1397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr13:96508534 C>T maps to NM_020121.3 R1295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr13:96624900 G>A maps to NM_020121.3 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr13:96506729 C>G did not map to a codon.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr2:64085068 C>A maps to NM_006759.3 S85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr2:64114601 G>T maps to NM_006759.3 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr2:64083558 G>T maps to NM_006759.3 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr2:234669200 G>T maps to NM_000463.2 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr2:234669391 C>T maps to NM_000463.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr2:234669121 C>T maps to NM_000463.2 D63D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr2:234680955 G>A maps to ENST00000373460 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr2:234545236 C>T maps to NM_019075.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:234545482 A>C maps to NM_019075.2 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:234621762 C>G maps to NM_019078.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr2:234622084 C>T maps to NM_019078.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr2:234622134 G>C maps to NM_019078.1 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr2:234526523 A>T maps to NM_019076.4 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr2:234526406 G>C maps to NM_019076.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:234580785 C>A maps to ENST00000373460 S69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:70455265 C>A maps to ENST00000514019 G636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:70513236 C>T maps to ENST00000514019 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr4:69798422 G>A maps to NM_024743.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr4:69817334 C>T maps to NM_024743.3 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr4:69692211 C>T maps to NM_001075.4 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr4:69696435 C>T maps to NM_001075.4 R476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr4:70066402 G>A maps to NM_001073.1 Q449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr4:69535708 C>A maps to NM_001076.2 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:69434193 C>T maps to NM_001076.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr4:69403561 C>T maps to NM_001076.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr4:69520864 A>C maps to NM_001076.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr4:70146226 G>A maps to NM_053039.1 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr4:70359495 C>T maps to NM_021139.2 W262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:70346408 T>C maps to NM_021139.2 K510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr4:70359470 G>C maps to NM_021139.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr4:70361309 G>A maps to NM_021139.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr4:70361045 G>A maps to NM_021139.2 Y178Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:69962753 C>T maps to NM_001074.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:35957425 G>C maps to NM_152404.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr5:35954390 G>A maps to NM_152404.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:36035958 G>A maps to NM_174914.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr5:36049522 C>T did not map to a codon.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr5:36038077 C>T maps to NM_174914.3 Q372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr4:115544701 C>T maps to NM_003360.3 Y222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:162468056 C>T maps to NM_175866.4 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:162467948 C>T maps to NM_175866.4 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:4944428 C>T maps to ENST00000398240 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr19:4941877 C>T maps to ENST00000398240 C349C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:4910992 C>A maps to ENST00000398240 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:4911004 C>T maps to ENST00000398240 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr19:4944247 C>G maps to ENST00000398240 S406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr19:4929328 C>G maps to ENST00000398240 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr6:34824634 C>T maps to NM_017754.3 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr6:34802628 C>G maps to NM_017754.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr6:34826145 G>A maps to NM_017754.3 Q671Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr6:34826514 G>A maps to NM_017754.3 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr6:34824634 C>T maps to NM_017754.3 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr6:34838658 G>A maps to NM_017754.3 L1249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr6:34838883 C>T maps to NM_017754.3 I1324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr6:34827249 C>T maps to NM_017754.3 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr6:34789558 C>A maps to NM_017754.3 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr6:34840211 C>G maps to NM_017754.3 L1440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr12:100452660 A>C maps to NM_015054.1 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr12:100476854 G>C maps to NM_015054.1 S449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:100452765 C>T maps to NM_015054.1 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr12:100452654 C>G maps to NM_015054.1 S800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr12:100502271 T>C maps to NM_015054.1 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:100433481 C>T maps to NM_015054.1 L1389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr9:6413597 C>T maps to NM_152896.1 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr5:176335532 C>T maps to ENST00000377219 K614K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:150387241 G>A maps to NM_024518.1 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:150387101 C>T maps to NM_024518.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr12:132403818 G>A maps to NM_003565.2 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:132380332 G>A maps to NM_003565.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr12:132404536 G>C maps to NM_003565.2 L939L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:132404620 C>G maps to NM_003565.2 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr17:19741843 G>A maps to NM_014683.3 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr15:75134484 G>A maps to NM_001099436.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr15:75132944 C>T maps to NM_001099436.1 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:41746764 C>T maps to NM_017886.2 T889T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:41877424 G>A maps to NM_017886.2 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr3:41938430 C>T maps to NM_017886.2 Q471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr16:20357600 C>T maps to ENST00000424589 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr16:20352630 G>A maps to ENST00000424589 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr16:20352497 G>A maps to ENST00000424589 R531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr16:20344665 G>T maps to ENST00000424589 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr16:20359620 C>T maps to ENST00000424589 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr21:43535989 G>C maps to NM_173568.3 R918R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:43543260 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr21:43510465 A>G maps to NM_173568.3 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr21:43504215 C>T maps to NM_173568.3 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr21:43543118 C>T maps to NM_173568.3 I1130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr21:43510537 G>A maps to NM_173568.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr21:43522336 C>T maps to NM_173568.3 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr21:43524189 C>T maps to NM_173568.3 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr21:43510516 G>A maps to NM_173568.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr21:43529670 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:124456778 C>G maps to NM_000373.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:124456863 C>T maps to NM_000373.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr3:124449458 G>A maps to NM_000373.3 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr3:124458995 G>T maps to NM_000373.3 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:26879508 G>A maps to NM_005148.3 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr17:26874857 G>A maps to NM_005148.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr17:26874707 G>A maps to NM_005148.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr12:121154714 G>T maps to NM_001080533.1 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr19:17729717 G>A maps to ENST00000428389 L1530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr19:17759245 G>A maps to ENST00000428389 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr19:17756807 G>A maps to ENST00000428389 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:17737461 G>A maps to ENST00000428389 I1439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr19:17752224 G>A maps to ENST00000428389 V959V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr19:17752248 G>A maps to ENST00000428389 D951D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr9:35382428 C>T maps to ENST00000396787 I840I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr9:35396569 C>T maps to ENST00000396787 V1065V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr9:35377477 G>A maps to ENST00000396787 K546K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr9:35381167 G>T maps to ENST00000396787 E746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr15:54306222 C>T maps to ENST00000260323 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr15:54306930 C>T maps to ENST00000260323 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr15:54435218 C>T maps to ENST00000260323 S996S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr15:54586191 T>C maps to ENST00000260323 D1306D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr15:54527297 C>T maps to ENST00000260323 R1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr15:54306189 G>T maps to ENST00000260323 G364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr17:73832316 G>A maps to ENST00000412096 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:73839335 G>C maps to ENST00000412096 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:73830497 G>A maps to ENST00000412096 Q736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:73840376 G>A maps to ENST00000412096 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr17:73830164 C>G maps to ENST00000412096 L786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr15:91491882 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:91483661 C>T maps to NM_018671.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr15:91496416 C>T maps to NM_018671.3 D818D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr15:91491501 C>T maps to NM_018671.3 Q576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:33482389 C>T maps to NM_173167.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr17:33495334 C>A maps to NM_173167.2 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr17:33475380 G>A maps to NM_173167.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:33486490 G>A maps to NM_173167.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr2:99234706 G>A maps to ENST00000409347 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr2:99226440 G>A maps to ENST00000409347 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr5:176305280 C>T maps to NM_133369.2 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:176304244 G>A maps to NM_133369.2 E477E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr5:176295921 C>T maps to NM_133369.2 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr10:73051480 C>T maps to NM_170744.3 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr10:73050726 C>T maps to NM_170744.3 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr4:96140353 G>A maps to NM_003728.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr4:96123971 G>C maps to NM_003728.3 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr4:96090503 G>A maps to NM_003728.3 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr4:96090483 C>T maps to NM_003728.3 Q899Q. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-ZF-A9R7-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr4:96106199 G>A maps to NM_003728.3 Q762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr6:41002619 G>C maps to NM_173561.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr6:41001720 G>A maps to NM_173561.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr6:41001768 G>C maps to NM_173561.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr8:35579726 G>C did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:35541108 C>T maps to ENST00000416672 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr8:35406936 G>A maps to ENST00000416672 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:35631842 C>T maps to ENST00000416672 F840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr8:35583707 C>T maps to ENST00000416672 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr8:35624514 C>A maps to ENST00000416672 S808S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr8:35583865 G>A maps to ENST00000416672 E505E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:167709657 G>A maps to NM_018974.3 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr6:167704997 C>T maps to NM_018974.3 N7N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr6:167711430 A>G did not map to a codon.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr6:167719500 C>T maps to NM_018974.3 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr11:67770562 G>T maps to NM_030930.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr12:109536370 C>T maps to NM_080911.2 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr12:109536205 C>G maps to NM_003362.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr12:109536301 G>A maps to NM_080911.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:73813468 C>T maps to NM_001080419.1 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr17:73780918 G>C maps to NM_001080419.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr17:73814728 C>T maps to NM_001080419.1 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr17:73812971 G>A maps to NM_001080419.1 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:1416390 G>A maps to ENST00000508903 I684I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr16:1417785 C>G maps to ENST00000508903 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr22:24916414 C>T maps to NM_016327.2 C284C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:18968268 G>C maps to ENST00000418384 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:18963839 G>A maps to ENST00000418384 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr19:18971667 G>T maps to ENST00000418384 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:18956811 G>A maps to ENST00000418384 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr19:18967816 C>T maps to ENST00000418384 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:18965702 G>A maps to ENST00000418384 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:18968283 C>G maps to ENST00000418384 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:18965817 C>T maps to ENST00000418384 Q477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr19:18963050 C>T maps to ENST00000418384 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr19:18968214 C>T maps to ENST00000418384 F696F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:12071354 T>C maps to NM_015542.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr10:12070787 C>A maps to NM_015542.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr13:115057171 G>T maps to NM_023011.2 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr23:118968907 C>T did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:118977196 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr23:118985778 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr23:118972484 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr23:118971835 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr23:118971858 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:36159495 C>T maps to NM_007000.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr19:36159434 C>G maps to NM_007000.2 S55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr3:118906761 C>T maps to NM_006952.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr3:118906731 G>A maps to NM_006952.3 W60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:118827611 C>G maps to NM_006760.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:118827674 C>T maps to NM_006760.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr11:118828035 C>A maps to NM_006760.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr22:45689062 C>G maps to NM_006953.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr22:45689101 G>A maps to NM_006953.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:76143380 C>T maps to NM_030570.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr2:158980393 C>G maps to NM_001135098.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr23:74494353 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr23:74494399 G>A did not map to a codon.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr23:74513343 C>T did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:74519604 C>G did not map to a codon.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr23:74494185 G>T did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:33891805 G>A maps to NM_018244.4 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr20:33891824 C>T maps to NM_018244.4 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr22:30163498 C>T maps to ENST00000406782 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:48641042 G>A maps to NM_003365.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr3:48642087 C>T maps to NM_003365.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:21991876 G>C maps to NM_003366.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr16:21968617 G>A maps to NM_003366.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr19:29698895 A>G maps to NM_006003.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr19:29698511 G>C maps to NM_006003.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr1:46775858 G>A maps to NM_006004.2 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:229771853 C>T maps to NM_014777.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:229773837 C>T maps to NM_014777.2 Q1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:229773863 C>T maps to NM_014777.2 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:229773885 C>T maps to NM_014777.2 Q1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:229779296 C>T maps to NM_014777.2 Q1218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr1:229773662 C>A maps to NM_014777.2 L1101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:43917867 C>G maps to NM_001077663.1 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:43916934 G>C maps to NM_001077663.1 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr7:43918317 C>T maps to NM_001077663.1 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr7:43916400 G>A maps to NM_001077663.1 P887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr7:43917823 G>C maps to NM_001077663.1 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr7:43918485 G>A maps to NM_001077663.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr9:131151577 G>A maps to NM_001135947.1 W76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr3:126208203 C>T maps to NM_001165974.1 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:126208125 G>A maps to NM_001165974.1 F627F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr3:126224594 C>G maps to NM_001165974.1 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr3:126202238 C>T maps to NM_001165974.1 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:45480181 C>T maps to NM_000374.4 Y236Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr10:127486690 G>A maps to NM_000375.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:17330598 C>T maps to NM_018467.3 R253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:17327007 C>T maps to NM_018467.3 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr1:161010080 G>A maps to NM_007122.3 Q252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr11:17538983 A>G maps to NM_005709.3 D416D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr11:17548812 G>A maps to NM_153676.3 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:17542915 C>T maps to NM_153676.3 E354E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr11:17544787 G>A maps to NM_153676.3 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr11:17552801 C>A maps to NM_153676.3 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr17:72916237 G>A maps to NM_173477.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:216591899 G>A maps to ENST00000366943 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:215916587 G>A maps to ENST00000366943 Q3827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:215955511 G>A maps to ENST00000366943 R3538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:216108114 C>T maps to ENST00000366943 L2381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr1:215953233 T>C maps to ENST00000366943 K3630K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr1:215807815 C>T maps to ENST00000366943 P5094P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr1:216052314 C>T maps to ENST00000366943 L2783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:216052272 T>A maps to ENST00000366943 S2797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:215901488 C>T maps to ENST00000366943 L3983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr1:215901488 C>T maps to ENST00000366943 L3983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:216498862 C>A maps to ENST00000366943 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:215848733 C>T maps to ENST00000366943 L4173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr1:215990452 T>C maps to ENST00000366943 P3152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr1:216595618 C>T maps to ENST00000366943 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:216017647 G>A maps to ENST00000366943 I3082I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr19:17370490 G>A maps to NM_031941.3 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr19:17367353 G>A maps to NM_031941.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:17373411 C>T maps to NM_031941.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:17373468 C>T maps to NM_031941.3 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr1:62914229 C>T maps to NM_003368.4 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr16:84778353 A>G maps to NM_005153.2 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr16:84792991 C>T maps to NM_005153.2 C436C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr23:47092404 C>T did not map to a codon.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr23:47104310 G>A did not map to a codon.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr23:47100680 C>A did not map to a codon.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr23:47092357 C>T did not map to a codon.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr23:47092453 C>T did not map to a codon.
Sequencing variant TCGA-K4-A5RI-01A-11D-A289-08 chr23:47101902 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr23:47104476 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr23:47102075 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:47101873 G>C did not map to a codon.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr13:27669914 T>C maps to NM_182488.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr13:27680081 C>G did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:179448466 C>G maps to NM_003940.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr3:179458160 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:179371084 C>T maps to NM_003940.2 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:179470093 C>T maps to NM_003940.2 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr18:209993 G>A maps to NM_005151.3 Q396Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr18:163450 A>T maps to NM_005151.3 K54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr12:62783260 A>G maps to ENST00000280377 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr12:62777938 A>G maps to ENST00000280377 K443K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:62785201 G>A maps to ENST00000280377 R742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:62790134 G>C maps to ENST00000280377 L877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:62785090 G>C maps to ENST00000280377 T705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr21:30426151 C>G maps to NM_006447.2 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr8:11996071 C>T maps to NM_201402.2 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr8:11995858 G>A maps to NM_201402.2 H137H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr8:11995990 A>T maps to NM_201402.2 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr3:49152978 G>A maps to ENST00000434032 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:119228515 C>A maps to NM_004205.4 R484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr11:119243761 T>C maps to NM_004205.4 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr11:119244115 C>T maps to NM_004205.4 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:132630420 G>C maps to NM_001008563.3 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr9:132642524 G>A maps to NM_001008563.3 K906K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:132618638 G>A maps to NM_001008563.3 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr9:132637006 G>A maps to NM_001008563.3 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:161132480 C>T maps to NM_012475.4 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr1:161132714 G>A maps to NM_012475.4 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr1:161132741 C>G maps to NM_012475.4 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr17:20907527 G>A maps to ENST00000455117 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:20919101 G>C maps to ENST00000455117 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr17:20916183 G>A maps to ENST00000455117 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr17:20931927 G>C maps to ENST00000455117 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr1:55555413 C>G did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:55566514 C>T maps to NM_015306.2 W1756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr1:55622626 C>T maps to NM_015306.2 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr1:55562760 G>A maps to NM_015306.2 R1934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr21:17150260 C>T maps to ENST00000285681 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr21:17150310 G>A maps to ENST00000285681 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr21:17203739 C>T maps to ENST00000285681 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr21:17250766 C>T maps to ENST00000285681 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr21:17205838 G>A maps to ENST00000285681 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr23:132161287 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr23:132161711 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:132162128 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr23:132160984 C>T did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:132160658 A>G did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:132161615 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:132161944 G>A did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr11:113686081 G>A maps to NM_020886.2 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:113697973 G>A maps to NM_020886.2 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:113683112 G>A maps to NM_020886.2 I619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr11:113679917 G>C maps to NM_020886.2 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:113674599 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr11:113674599 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr11:113679871 C>A maps to NM_020886.2 E693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr11:113711319 C>T maps to NM_020886.2 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr19:57641056 G>A maps to NM_020903.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr15:63852115 G>A maps to NM_006537.2 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr15:63882937 G>C maps to NM_006537.2 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr16:23099152 A>G maps to NM_020718.3 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:23119405 G>C maps to NM_020718.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr16:23098410 A>C did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr16:23085190 C>T maps to NM_020718.3 K729K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr17:58260574 C>G maps to NM_032582.3 L1358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr17:58348773 G>A maps to NM_032582.3 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:58313540 G>A maps to NM_032582.3 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:58422943 C>T maps to NM_032582.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:58288741 G>C maps to NM_032582.3 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:58260691 G>A maps to NM_032582.3 L1319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr17:58282945 G>A maps to NM_032582.3 F1037F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr17:58275712 C>T maps to NM_032582.3 R1114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr17:58275805 C>T did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:58285485 C>G maps to NM_032582.3 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr17:58365901 G>A maps to NM_032582.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr17:58365911 G>A maps to NM_032582.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:58289432 C>A maps to NM_032582.3 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr17:58300840 C>T maps to NM_032582.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:78163602 A>G maps to NM_015017.3 P872P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:78177466 T>A maps to NM_015017.3 K822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:78204947 A>G did not map to a codon.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr2:61607464 G>A maps to NM_014709.3 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr2:61417468 C>T maps to NM_014709.3 Q3270Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr2:61441806 G>T maps to NM_014709.3 S2690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:61416072 C>T maps to NM_014709.3 E3335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr2:61528240 G>A maps to NM_014709.3 Q1325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr2:61473532 T>A maps to NM_014709.3 G2158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:61415237 C>G maps to NM_014709.3 *3547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:61575065 G>A maps to NM_014709.3 R742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr2:61607486 G>T maps to NM_014709.3 C277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr11:77924858 A>G maps to NM_020798.2 *1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr11:77924750 G>T maps to NM_020798.2 P983P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr11:77907437 C>T maps to NM_020798.2 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr11:77919931 C>G maps to NM_020798.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr11:77921513 T>A maps to NM_020798.2 A871A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr11:77911808 C>T maps to NM_020798.2 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr11:77909063 C>T maps to NM_020798.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr11:77921318 C>T maps to NM_020798.2 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:77917003 G>A maps to NM_020798.2 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr17:76794516 G>A maps to NM_025090.3 L1119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:76831482 G>A maps to NM_025090.3 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:76810610 G>A maps to NM_025090.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr17:76816040 C>T maps to NM_025090.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr17:76832340 G>A maps to NM_025090.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr2:219360634 C>A maps to NM_020935.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr2:219339479 C>G maps to NM_020935.2 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr2:219414541 G>C maps to NM_020935.2 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr2:219423303 C>A maps to NM_020935.2 G25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr4:144127184 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:144124644 G>T maps to NM_032557.5 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr4:144134959 G>T maps to NM_032557.5 E611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr4:144107019 G>A maps to NM_032557.5 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr2:85866453 C>T maps to NM_006590.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:85843586 G>A did not map to a codon.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr3:49365237 G>A maps to NM_003363.3 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr3:49323706 G>C maps to NM_003363.3 S675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr3:49363262 G>A maps to NM_003363.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr3:49336022 C>A maps to NM_003363.3 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr3:49321490 G>A maps to NM_003363.3 V823V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:234460030 A>G maps to NM_018218.2 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:234386115 G>A maps to NM_018218.2 I1222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:6189332 C>T maps to ENST00000404835 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr17:9631803 G>T maps to NM_153210.3 E957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr17:9559743 C>T maps to NM_153210.3 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:9580107 C>T maps to NM_153210.3 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr12:95918478 G>C maps to NM_032147.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr12:95926830 G>T maps to NM_032147.2 S401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr6:99885182 C>G maps to NM_001080481.1 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr11:11955431 G>T maps to ENST00000399455 E614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr11:11963916 G>A maps to ENST00000399455 Q790Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr11:11913615 C>T maps to ENST00000399455 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:11957848 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:11958016 G>A maps to ENST00000399455 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr11:11972016 G>T maps to ENST00000399455 E1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:11964243 C>G maps to ENST00000399455 L899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr11:11964063 G>T maps to ENST00000399455 V839V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr1:22056205 G>A maps to NM_032236.5 Q431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:22048159 C>T maps to NM_032236.5 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:22048201 C>T maps to NM_032236.5 K568K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr1:22055167 C>A maps to NM_032236.5 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr6:41766415 C>T maps to NM_018561.3 *641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr6:41774067 G>A maps to ENST00000373009 D218D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr12:6965238 G>A maps to NM_001098536.1 K121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:6973992 C>T maps to NM_001098536.1 I784I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:6968693 C>T maps to NM_001098536.1 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr23:55514286 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr23:55514286 C>G did not map to a codon.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr23:55515339 G>A did not map to a codon.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr4:120193093 C>T maps to NM_019050.2 H693H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr4:120213549 C>A maps to NM_019050.2 P802P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr4:120169948 C>G maps to NM_019050.2 S95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr10:75277426 G>A maps to NM_152586.3 A919A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr10:75279709 C>A maps to NM_152586.3 T841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:75289663 C>A maps to NM_152586.3 E612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr10:75258707 G>A maps to NM_152586.3 G1578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr10:75283446 C>T maps to NM_152586.3 A752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr10:75279564 G>A maps to NM_152586.3 Q890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr10:75301467 G>A maps to NM_152586.3 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr10:75277408 T>C maps to NM_152586.3 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:5037246 G>A maps to NM_004505.2 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:5041506 C>T maps to NM_004505.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:5074101 C>T maps to NM_004505.2 G1282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:5037201 G>A maps to NM_004505.2 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr17:5039176 C>T maps to NM_004505.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr17:5073858 G>A maps to NM_004505.2 G1201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr17:5039968 G>C maps to NM_004505.2 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr10:11505381 G>A maps to NM_001080491.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:8996317 G>A maps to NM_003470.2 R621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:9014214 C>T did not map to a codon.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr16:8989599 T>A did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:8999044 C>T maps to NM_003470.2 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:9017103 G>A maps to NM_003470.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:50769683 G>A maps to NM_005154.3 K402K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:50769146 C>T maps to NM_005154.3 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr15:50773823 C>T maps to NM_005154.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr15:50785036 T>C maps to NM_005154.3 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr23:41027316 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr23:41047251 G>C did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:41077662 A>T did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr23:41075731 A>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:41010203 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr23:41025164 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:41007693 G>A did not map to a codon.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr23:41057841 G>A did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:41027282 T>G did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:41027292 T>G did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:41088554 G>C did not map to a codon.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr23:41029730 A>T did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:41060454 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:41029373 T>C did not map to a codon.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr23:41060385 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:41084103 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr23:41056736 G>A did not map to a codon.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr24:14848136 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr24:14832566 C>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr24:14885573 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr24:14885803 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr24:14885823 G>T did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr24:14898190 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr24:14958274 C>A did not map to a codon.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr24:14952194 G>T did not map to a codon.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr24:14952493 G>T did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr24:14958934 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr24:14847562 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr24:14837149 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr24:14838583 T>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr24:14952352 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr13:31216886 C>T maps to NM_005800.4 Q369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr13:31205592 C>T maps to NM_005800.4 Q284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:31233465 C>T maps to NM_005800.4 F1084F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr13:31231833 C>G maps to NM_005800.4 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr13:31221067 G>A did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr6:149262464 G>A maps to NM_005715.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr1:38489279 C>T maps to NM_016037.3 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr23:129041399 G>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr23:129042092 G>C did not map to a codon.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr23:129042667 G>A did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr23:129059058 C>G did not map to a codon.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr23:129045884 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:129053375 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr23:129055394 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr23:129058891 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr23:129058885 G>A did not map to a codon.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr13:52604241 C>T maps to NM_021645.5 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr13:52604155 G>T maps to NM_021645.5 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr17:49340654 G>C maps to NM_016001.2 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr17:49340654 G>C maps to NM_016001.2 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr17:49365434 C>T maps to NM_016001.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr17:49374339 C>G maps to NM_016001.2 S554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr17:49371316 G>A maps to NM_016001.2 K519K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr12:101731837 T>C maps to NM_014503.2 P1217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:101699773 A>T maps to NM_014503.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:117782535 G>C maps to NM_032334.2 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr4:71554784 C>T maps to NM_020368.2 Q131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:71555248 G>T maps to NM_020368.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:30195094 G>A maps to NM_018428.2 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:30192427 T>C maps to NM_018428.2 E531E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr17:30205745 G>C maps to NM_018428.2 S341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:144803391 C>T maps to NM_007124.2 L1185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:145160370 G>A maps to NM_007124.2 L3376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr6:144820448 G>A maps to NM_007124.2 K1550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:144782331 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:144832184 G>T maps to NM_007124.2 E1624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr6:144869905 G>T maps to NM_007124.2 L2242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr6:144800974 G>T maps to NM_007124.2 E1122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr6:145051533 G>C maps to NM_007124.2 L2617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr6:144613023 T>C maps to NM_007124.2 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr6:144860467 C>G maps to NM_007124.2 L2136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr6:144814559 C>T maps to NM_007124.2 L1521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr6:144783999 G>T maps to NM_007124.2 E1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr6:144835910 G>A maps to NM_007124.2 L1733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr6:145156990 C>T maps to NM_007124.2 S3247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr6:144999631 G>T maps to NM_007124.2 E2524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr6:144844192 A>T maps to NM_007124.2 A1925A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:144803403 C>T maps to NM_007124.2 I1189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:7907828 G>C maps to NM_006786.3 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr1:7913461 G>A maps to NM_021995.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr3:190993106 C>A maps to NM_198152.3 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr17:80333363 G>A maps to NM_018949.1 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr24:15591421 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr24:15478204 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr24:15467872 C>G did not map to a codon.
Sequencing variant TCGA-E7-A519-01A-11D-A26M-08 chr24:15438104 A>G did not map to a codon.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr24:15469784 G>T did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr24:15582005 G>C did not map to a codon.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr24:15435626 G>C did not map to a codon.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr24:15466933 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr24:15591140 A>G did not map to a codon.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr11:75672571 C>G maps to NM_003369.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:106729127 G>A maps to ENST00000283148 Q285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr23:47518320 C>T did not map to a codon.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr16:70834773 G>T maps to NM_018052.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr16:70817457 C>A did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:70778473 C>T maps to NM_018052.3 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr16:70815874 C>T maps to NM_018052.3 W281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:6575145 C>G maps to ENST00000396308 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr17:8064982 G>T maps to ENST00000488857 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:85818939 G>C maps to NM_006634.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:155169447 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:155171705 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr23:155171702 G>C did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr1:116227976 G>A maps to NM_001172412.1 Q381Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:116206871 C>T maps to NM_001172412.1 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr1:160394990 G>A maps to NM_020335.2 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:160389331 C>T maps to NM_020335.2 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:160388961 C>G maps to NM_020335.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:160389174 C>T maps to NM_020335.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:160388871 C>T maps to NM_020335.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:56993381 C>T maps to NM_004738.4 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr20:57014065 A>T maps to NM_004738.4 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr6:31750903 G>A maps to NM_006295.2 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr6:30884991 G>A maps to NM_001167734.1 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr14:77242312 C>T maps to NM_014909.4 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr14:77242468 G>A maps to NM_014909.4 K255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:4432842 C>G maps to NM_138440.2 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:4431069 C>T maps to NM_138440.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:46026925 G>A maps to NM_003370.3 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:41174208 G>T maps to NM_006373.3 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr17:41168326 C>T maps to NM_006373.3 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr17:41169885 C>T maps to NM_006373.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr16:77910311 G>T maps to NM_020927.1 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr16:77859261 C>T maps to NM_020927.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr16:77896682 C>T maps to NM_020927.1 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:6829859 C>T maps to NM_005428.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr19:6836571 G>A maps to NM_005428.2 W636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:6843174 C>T maps to NM_005428.2 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr19:6772886 G>C maps to NM_005428.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr9:136804248 G>T maps to NM_001134398.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr9:136634578 G>A maps to NM_001134398.1 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr9:136857250 G>C maps to NM_001134398.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr9:136671207 C>T maps to NM_001134398.1 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:108185291 G>A maps to NM_006113.4 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:118891966 C>A maps to NM_199131.2 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:101194672 T>C maps to NM_001078.3 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr1:101190237 C>T maps to NM_001078.3 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:101200295 A>G maps to NM_001078.3 Q677Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr1:101198218 G>T maps to NM_001078.3 E591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:101194768 C>T maps to NM_001078.3 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr5:82789628 C>T maps to NM_004385.4 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr5:82849279 C>T maps to NM_004385.4 C3197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:82835571 G>A maps to NM_004385.4 E2250E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:82850805 C>T maps to NM_004385.4 L3228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr5:82835421 T>A maps to NM_004385.4 T2200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr5:82833906 A>G maps to NM_004385.4 Q1695Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr5:82836782 C>G maps to NM_004385.4 S2654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr5:82817721 C>T maps to NM_004385.4 I1199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr5:82789631 C>T maps to NM_004385.4 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr10:75849104 C>T maps to NM_014000.2 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr9:35059693 G>A maps to NM_007126.3 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr9:35062087 G>A maps to NM_007126.3 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr9:35062057 C>T maps to NM_007126.3 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr8:67577612 T>C maps to NM_025054.4 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr8:67578332 C>T maps to NM_025054.4 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr8:67563732 C>T maps to NM_025054.4 Q919Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr23:7811786 G>A did not map to a codon.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr23:7811697 G>A did not map to a codon.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr23:6451815 C>T did not map to a codon.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr23:8433507 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr5:133326752 C>T maps to NM_003374.2 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr10:76978943 C>T maps to NM_001184783.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr10:76990692 G>A maps to NM_001184783.1 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr8:42260957 G>A maps to ENST00000417062 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr12:48250913 G>C maps to NM_001017535.1 S194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr12:48272842 C>G maps to NM_001017535.1 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:43748496 C>T maps to NM_001025366.2 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr6:43738905 G>T maps to NM_001025366.2 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:43752297 G>C maps to NM_001025366.2 *413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr4:177713369 G>A maps to NM_005429.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr4:177608516 G>C maps to NM_005429.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr4:177608357 G>A maps to NM_005429.2 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr10:135053698 G>A maps to NM_014468.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:135053569 C>T maps to NM_014468.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr3:157099132 C>T maps to NM_001167912.1 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr3:156983383 G>A maps to NM_001167912.1 F732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:157081390 C>T maps to NM_001167912.1 E499E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr3:156983395 G>A maps to NM_001167912.1 V728V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:156983404 C>T maps to NM_001167912.1 E725E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr3:157177908 G>C maps to NM_001167916.1 S197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr12:95656755 G>T maps to NM_017599.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:95660223 C>T maps to NM_017599.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr12:95676321 G>T maps to NM_017599.3 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:100806759 G>A maps to NM_003378.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr7:100806714 G>A maps to NM_003378.3 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr7:100808034 C>T maps to NM_003378.3 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A5UA-01A-11D-A289-08 chr6:117591919 G>A maps to NM_182645.2 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr6:117589355 T>A maps to NM_182645.2 Y31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr6:117589355 T>C maps to NM_182645.2 Y31Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:87018079 A>G maps to NM_016206.2 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:10183797 C>T maps to NM_000551.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:10191495 C>T maps to NM_000551.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:156268785 G>A maps to NM_001004319.2 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr2:219290519 C>T maps to NM_007127.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr2:219292747 C>T maps to NM_007127.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:219305491 C>G maps to NM_007127.2 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr2:219294198 C>G maps to NM_007127.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr3:38047992 C>A maps to NM_015873.3 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr3:38039652 G>A maps to NM_015873.3 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr3:38042960 G>A maps to NM_015873.3 Q399Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr3:38043071 G>T maps to NM_015873.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr3:38043287 G>A maps to NM_015873.3 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A8S6-01A-31D-A38G-08 chr3:38038626 G>A maps to NM_015873.3 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:17276804 C>T maps to NM_003380.3 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:17277883 G>A maps to NM_003380.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:17277193 T>C maps to NM_003380.3 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr10:17275815 C>T maps to NM_003380.3 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr10:17277883 G>C maps to NM_003380.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr6:153073416 C>T maps to NM_003381.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr6:153075324 G>A maps to NM_003381.2 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr14:77894752 G>C maps to ENST00000445370 S500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr14:77909468 C>G maps to ENST00000445370 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr14:77896089 C>T maps to ENST00000445370 K426K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:42573762 C>T maps to NM_004624.3 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr3:42577694 G>T maps to NM_004624.3 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr3:42568980 C>T maps to NM_004624.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:42573804 G>A maps to NM_004624.3 K330K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr3:42576580 C>T maps to NM_004624.3 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:42573309 C>A maps to NM_004624.3 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr7:158824560 C>T did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr7:158826992 G>A maps to ENST00000402066 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr7:158824637 C>T maps to ENST00000402066 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr7:158827297 G>A maps to ENST00000402066 R426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr7:158935194 G>A maps to ENST00000402066 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr7:158824527 C>T maps to ENST00000402066 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr2:36994238 G>T maps to NM_053276.3 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:37041502 G>A maps to NM_053276.3 *694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:36994258 G>A maps to NM_053276.3 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr7:65338471 G>A maps to NM_173517.3 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr7:65419175 C>T maps to NM_173517.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr23:150573405 A>G did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr17:4689473 G>A maps to NM_182566.2 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:57967071 G>A maps to NM_020633.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr19:53762815 A>G maps to NM_173856.2 *396W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr19:53770825 G>A maps to NM_173857.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr6:133004431 C>T maps to NM_004666.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:133070890 C>T maps to NM_004665.2 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr6:133072385 G>A maps to NM_004665.2 C366C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr6:133070832 C>A did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr3:51457414 C>A maps to ENST00000273612 T1003T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr22:24095143 G>T maps to ENST00000405618 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr11:118948932 G>A maps to NM_021729.4 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr11:118949690 C>G maps to NM_021729.4 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr11:118949690 C>T maps to NM_021729.4 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr9:79960013 C>G maps to ENST00000376646 L2415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr9:79890499 A>C maps to ENST00000376646 R867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr9:79898508 C>T maps to ENST00000376646 N1094N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr9:79852954 T>C maps to ENST00000376646 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr9:79934556 G>T maps to ENST00000376646 E1795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr9:79973271 G>T did not map to a codon.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr8:100847779 T>C maps to NM_017890.3 F3277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr8:100403870 G>A maps to NM_017890.3 K1007K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:100454825 G>A maps to NM_017890.3 E1136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:100874103 G>T maps to NM_017890.3 R3740R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr8:100729480 G>A maps to NM_017890.3 L2204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr8:100866425 G>A maps to NM_017890.3 A3628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr8:100654523 A>G maps to NM_017890.3 S1927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr8:100443873 G>A maps to NM_017890.3 V1064V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr8:100866425 G>A maps to NM_017890.3 A3628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr8:100133669 C>T maps to NM_017890.3 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr8:100832283 A>G maps to NM_017890.3 L3001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr8:100654271 A>T maps to NM_017890.3 A1843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr8:100791180 G>A maps to NM_017890.3 V2592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr8:100829775 C>A maps to NM_017890.3 I2727I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr8:100832241 C>T maps to NM_017890.3 P2987P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:62167120 T>C maps to NM_020821.2 A3456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr15:62176468 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:62210340 G>T maps to NM_020821.2 S2585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:62217668 C>A maps to NM_020821.2 E2199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:62223290 C>T maps to NM_020821.2 S2012S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr15:62182380 G>A maps to NM_020821.2 S3108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr15:62325657 G>A maps to NM_020821.2 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr15:62209731 G>C maps to NM_020821.2 V2621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr15:62254673 C>A maps to NM_020821.2 E1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr15:62219319 G>C maps to NM_020821.2 L2162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:62226530 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr15:62254953 A>G maps to NM_020821.2 H1143H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr15:62237951 G>A maps to NM_020821.2 Q1704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:12333104 C>T maps to NM_015378.2 Q717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:12337496 C>G maps to NM_015378.2 L1284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:12405436 C>T maps to NM_015378.2 T2964T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr1:12463959 C>G maps to NM_015378.2 L3988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr1:12336627 G>T maps to NM_015378.2 E995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:12304592 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:12387711 G>A maps to NM_015378.2 L2666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:12322039 G>A maps to NM_015378.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:12415987 G>T maps to NM_015378.2 E3238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr1:12317072 C>G maps to NM_015378.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr1:12461716 C>G maps to NM_015378.2 L3947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr1:12378314 G>T maps to NM_015378.2 V2445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr1:12371681 T>C maps to NM_015378.2 H2274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:12557565 G>A maps to NM_015378.2 Q4225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:12401927 C>T maps to NM_015378.2 T2906T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr1:12476780 G>A maps to NM_015378.2 L4078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:12429572 G>T maps to NM_015378.2 E3542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr1:12460347 G>T maps to NM_015378.2 V3915V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr1:12337331 C>T maps to NM_015378.2 N1229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr1:12327055 C>T maps to NM_015378.2 V571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:12446338 C>T maps to NM_015378.2 H3860H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr1:12443177 C>T maps to NM_015378.2 I3778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:12336611 G>A maps to NM_015378.2 K989K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr15:41192560 C>G maps to NM_020857.2 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr11:134114895 C>T maps to NM_052875.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr8:145649188 C>G maps to NM_016208.2 *222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr12:122729211 A>G maps to NM_022916.4 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr12:122720407 C>T maps to NM_022916.4 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr12:122717470 G>A maps to NM_022916.4 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr12:122723262 A>G maps to NM_022916.4 N391N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr15:91545328 G>A maps to NM_018668.3 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr16:46697017 G>A maps to NM_018206.4 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr16:46694416 G>A maps to NM_018206.4 S786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr16:46696328 G>A maps to NM_018206.4 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr16:46694553 G>A maps to NM_018206.4 Q741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr16:46716045 A>G maps to NM_018206.4 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr13:53024699 G>A maps to NM_016075.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:123380579 G>A maps to NM_024667.2 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr12:123355587 G>A maps to NM_024667.2 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr12:123355595 G>A maps to NM_024667.2 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr12:123380552 G>A maps to NM_024667.2 N19N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr15:42462050 C>T maps to ENST00000348544 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr15:42459725 G>A maps to ENST00000348544 Q426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:38860834 C>A maps to NM_014396.3 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr7:38813787 A>C maps to NM_014396.3 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr7:38805224 G>C maps to NM_014396.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr1:150053425 G>A maps to NM_007259.3 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:69354157 G>A maps to NM_013245.2 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr18:61078763 C>G maps to NM_004869.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr6:33238054 A>G maps to NM_022553.4 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:33236338 C>T maps to NM_022553.4 Q212Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr6:33235698 C>G maps to NM_022553.4 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr17:465900 G>A maps to NM_001128159.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:556595 C>T maps to NM_001128159.2 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr17:617915 C>A maps to NM_001128159.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr2:64208890 G>A maps to NM_016516.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr2:64160936 G>A maps to NM_016516.2 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr2:64189562 C>A maps to NM_016516.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr2:64148363 G>C maps to NM_016516.2 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:64189553 C>A maps to NM_016516.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr2:64148439 G>C maps to NM_016516.2 S590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr2:64174579 C>T maps to NM_016516.2 K394K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr3:184557484 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:184633238 G>T maps to ENST00000437079 E787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr3:184675242 C>T maps to ENST00000437079 F1039F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:184566951 C>G maps to ENST00000437079 S212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:97313615 T>C maps to NM_003384.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr2:58311246 A>T maps to NM_001130480.2 K54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:50519311 G>T maps to NM_016440.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:107310213 G>A did not map to a codon.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr23:107301400 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr23:107319442 A>G did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:107316517 A>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:107319305 G>T did not map to a codon.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr23:107288383 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:118511774 C>T maps to NM_019086.5 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:118533367 G>A maps to NM_019086.5 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr12:118533469 C>A maps to NM_019086.5 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr11:124620667 G>T maps to NM_014312.3 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KQ-01A-11D-A38G-08 chr23:65253601 G>A did not map to a codon.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr23:65253340 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr23:65242173 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr23:65253366 C>G did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:65253644 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:159827691 C>A maps to NM_001013661.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr1:159825826 G>A maps to NM_001013661.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:159825785 G>A maps to NM_001013661.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:54545203 G>A maps to NM_198481.3 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr19:54561827 G>A maps to NM_198481.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr19:54545035 G>A maps to NM_198481.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:54544223 C>T maps to NM_198481.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:54561594 G>C maps to NM_198481.3 S107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr7:54617615 G>T maps to ENST00000404951 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr20:36572408 C>T maps to NM_080607.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr20:25059383 G>A maps to NM_199425.1 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr20:25059419 G>A maps to NM_199425.1 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FM-01A-11D-A38G-08 chr1:117695791 G>A maps to NM_024626.2 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:117699367 C>A maps to NM_024626.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr14:68118198 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:26696646 G>C maps to NM_000638.3 S137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr1:1374464 G>A maps to NM_022834.4 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr1:1374635 C>T maps to NM_022834.4 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr1:1372364 C>T maps to NM_022834.4 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:1374719 G>T maps to NM_022834.4 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:1372337 G>A maps to NM_022834.4 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr10:116049057 C>T maps to NM_198496.1 G644G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:22157564 G>C maps to NM_173615.3 V913V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr16:22143019 C>A maps to NM_173615.3 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr2:98846527 C>A maps to NM_144992.4 I722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:98779341 C>T maps to NM_144992.4 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr2:98828415 G>A maps to NM_144992.4 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr2:98920259 A>T maps to NM_144992.4 P1172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:98916600 T>G maps to NM_144992.4 P1114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr2:98804562 C>A maps to NM_144992.4 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr11:124007357 T>A maps to NM_014622.4 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr11:124006840 C>T maps to NM_014622.4 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr11:124007309 C>T maps to NM_014622.4 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:61026230 G>C maps to NM_152718.2 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:61058811 G>A maps to NM_152718.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:61039179 C>T maps to NM_152718.2 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr11:61034933 C>T maps to NM_152718.2 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr11:61026746 G>T maps to NM_152718.2 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:6161923 C>T maps to NM_000552.3 V657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr12:6078421 G>A maps to NM_000552.3 Q2562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr12:6091020 G>A maps to NM_000552.3 P2406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:6143928 G>A maps to NM_000552.3 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr12:6184555 C>T maps to NM_000552.3 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr12:6128365 C>T maps to NM_000552.3 K1406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RE-01A-11D-A38G-08 chr12:6182826 C>A maps to NM_000552.3 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:28897266 C>T maps to NM_016628.3 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr10:28899734 C>T maps to NM_016628.3 Q425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr10:28900788 C>T maps to NM_016628.3 Q459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr10:28903603 C>T maps to NM_016628.3 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr10:28824569 C>A maps to NM_016628.3 S53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr10:28897141 C>G maps to NM_016628.3 S316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr10:28908492 G>A maps to NM_016628.3 K634K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr10:28903527 G>T maps to NM_016628.3 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr10:28884770 C>T maps to NM_016628.3 H240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr10:88232507 G>C maps to ENST00000342368 S670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr14:100835427 G>C maps to NM_173701.1 S32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr14:100813089 G>A maps to NM_173701.1 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:119588230 G>A maps to NM_015836.3 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr23:48546836 G>A did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:48542301 G>C did not map to a codon.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr23:48542334 G>A did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr23:48547078 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr23:48547058 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr23:48547078 G>C did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr6:110423399 C>A maps to NM_003931.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr6:110434534 C>A maps to NM_003931.2 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr1:27734816 C>A maps to NM_006990.2 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BU-01A-31D-A26M-08 chr13:27257046 G>A maps to NM_006646.5 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr13:27216529 G>A maps to NM_006646.5 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr13:27256893 G>T maps to NM_006646.5 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr13:27246114 A>C maps to NM_006646.5 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr7:123388671 C>A maps to NM_003941.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:74686772 C>T maps to ENST00000452361 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr2:74687690 G>T maps to ENST00000393972 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr12:14943497 G>A maps to NM_016312.2 Q401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:42422776 C>G maps to NM_152613.2 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr22:42394845 C>T maps to NM_152613.2 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr22:42422821 C>T maps to NM_152613.2 Y189Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr23:102612723 G>A did not map to a codon.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr7:74486508 C>T maps to NM_030798.3 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr7:73275562 G>A maps to NM_182504.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr7:73279450 A>G maps to NM_182504.3 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr7:73275586 C>G maps to NM_182504.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:224782692 G>A maps to NM_020830.3 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr13:52158915 G>C maps to NM_052950.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr4:85611687 C>A maps to NM_014991.4 E3112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WY-01A-11D-A22Z-08 chr4:85617302 T>C maps to NM_014991.4 L2907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr4:85636458 G>C maps to NM_014991.4 V2651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr4:85722827 G>A maps to NM_014991.4 Q933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr4:85701311 G>C maps to NM_014991.4 V1438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr4:85742699 G>A maps to NM_014991.4 H376H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr4:85594021 C>T maps to NM_014991.4 *3527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr4:85634392 C>T did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr4:85634325 C>A maps to NM_014991.4 T2676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr4:85600101 C>A maps to NM_014991.4 E3373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PA-01A-11D-A38G-08 chr4:85645707 T>A maps to NM_014991.4 K2438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr4:85611799 T>C maps to NM_014991.4 E3074E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr4:85612876 C>T maps to NM_014991.4 Q3037Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr14:55424326 G>A maps to NM_007086.3 R910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr14:55462392 C>A maps to NM_007086.3 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr14:55462424 G>C maps to NM_007086.3 S350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr14:55467707 G>T maps to NM_007086.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr14:55411116 G>C maps to NM_007086.3 S1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr4:10100689 G>A maps to NM_017491.3 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr4:10083019 G>A maps to NM_017491.3 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr4:10100746 C>T maps to NM_017491.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr4:10084737 C>A maps to NM_017491.3 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr4:10079466 G>A maps to NM_017491.3 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr10:122622424 G>A maps to NM_018117.11 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr10:122664180 G>T maps to NM_018117.11 L1017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr10:122626259 C>A maps to NM_018117.11 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr10:122661813 G>A maps to NM_018117.11 Q911Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr10:122622379 T>A maps to NM_018117.11 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:203748981 A>G maps to NM_018256.3 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr23:48460203 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr23:48457330 C>T did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr23:48458083 G>C did not map to a codon.
Sequencing variant TCGA-FD-A6TI-01A-11D-A32B-08 chr23:48460451 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:48460561 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:9501560 C>T maps to NM_145054.4 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:9515733 T>C maps to NM_145054.4 D321D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:9541998 C>T maps to NM_145054.4 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:177083256 G>T maps to NM_170710.4 E952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr4:177058702 C>T maps to NM_170710.4 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr4:39233497 C>T maps to NM_025132.3 H688H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:39254831 G>C maps to NM_025132.3 L932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:39269685 C>A maps to NM_025132.3 I1111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr4:39229849 G>A maps to NM_025132.3 E550E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr14:102606454 C>G maps to ENST00000454394 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:102606454 C>T maps to ENST00000454394 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr14:102675931 G>A maps to ENST00000454394 E506E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr16:735418 G>C maps to ENST00000248142 V749V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr16:735980 C>A maps to ENST00000248142 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr14:100847803 A>G maps to NM_001161476.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr14:100996169 C>G maps to NM_001161476.1 S476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr1:224619464 G>A maps to NM_025160.6 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr1:224586673 C>T maps to NM_025160.6 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr6:170033159 G>A maps to NM_182552.3 I702I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr1:118477208 G>C maps to NM_006784.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:118496157 G>A maps to NM_006784.2 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:118486189 C>T maps to NM_006784.2 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:118485123 G>T maps to NM_006784.2 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr9:116094290 G>A maps to NM_001012361.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr2:128477564 C>T maps to NM_018383.4 Q678Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr2:128471203 G>A maps to NM_018383.4 F1087F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:128522768 G>A maps to NM_018383.4 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr9:131397155 G>A maps to NM_052844.3 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr9:131396646 G>A maps to NM_052844.3 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:131396189 C>A maps to NM_052844.3 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr9:131397987 C>A maps to NM_052844.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:20138059 G>A maps to NM_001006657.1 Q688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr2:20130163 C>T maps to NM_001006657.1 L1049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:20145701 G>A maps to NM_001006657.1 R575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr2:20114009 G>A maps to NM_001006657.1 I1061I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr5:110462532 C>T maps to NM_139281.2 F936F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr10:1123866 G>T maps to ENST00000416775 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr10:1142134 C>T maps to ENST00000416775 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr9:127617982 C>T maps to NM_001045476.1 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr21:44274682 G>C maps to NM_018669.4 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr5:76736793 G>A maps to NM_018268.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:117543581 A>G did not map to a codon.
Sequencing variant TCGA-CF-A9FF-01A-11D-A38G-08 chr23:117578405 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr23:117566846 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:117576549 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr23:117570745 C>G did not map to a codon.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr23:117526818 A>T did not map to a codon.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr23:117578413 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr23:117527215 A>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr23:117576205 G>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr23:48933318 C>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr23:48933319 T>G did not map to a codon.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr23:48933233 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:48933302 G>C did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr23:48932867 G>A did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:48932854 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr23:48933036 G>C did not map to a codon.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr23:48933375 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr23:48933236 A>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:80574487 G>A maps to NM_019613.3 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr6:33254943 C>T maps to NM_005452.5 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr6:33256754 C>T maps to NM_005452.5 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr6:33255416 G>A maps to NM_005452.5 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr6:33248648 G>A maps to NM_005452.5 Q411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:109533887 C>A maps to NM_001142550.1 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr3:39108241 C>T maps to NM_020839.2 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr3:39126134 G>A did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:167277881 A>G maps to NM_178824.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr3:167218046 C>A maps to NM_178824.3 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr3:167250741 G>A maps to NM_178824.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr3:113145000 G>C maps to NM_001164496.1 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:113098283 G>A maps to NM_001164496.1 Q723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr3:113085025 C>A maps to NM_001164496.1 G859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:113135450 G>A maps to NM_001164496.1 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr3:113098265 T>A maps to NM_001164496.1 K729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr3:113098266 C>T maps to NM_001164496.1 E728E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr3:196281453 C>A maps to NM_182627.1 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R5-01A-12D-A42E-08 chr3:196281408 G>A maps to NM_182627.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:74649499 C>T maps to NM_032118.2 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:74650037 C>T maps to NM_032118.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr5:140047878 C>T maps to NM_017706.4 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr5:140048529 C>G maps to NM_017706.4 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr16:74955919 A>G maps to NM_030581.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr16:74943791 C>T maps to NM_030581.3 Q471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr16:74949824 C>T maps to NM_030581.3 Q389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr16:74920260 C>T maps to NM_030581.3 W818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:74920243 C>A maps to NM_030581.3 E824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr3:49049836 C>T maps to NM_018031.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr3:49051450 C>T maps to NM_018031.3 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:49049461 G>A maps to NM_018031.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr3:49050913 C>T maps to NM_018031.3 H679H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr3:49052719 G>C maps to NM_018031.3 *1152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr7:158715119 C>G maps to NM_018051.4 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:158723186 C>T maps to NM_018051.4 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr7:158662583 C>G maps to NM_018051.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr19:36593976 G>A did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr19:36558746 C>T maps to NM_001083961.1 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:85561639 C>A maps to NM_145172.3 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:85561675 C>A maps to NM_145172.3 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr1:241920613 G>T maps to NM_144625.4 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr1:241951204 C>G maps to NM_144625.4 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:241951318 G>A maps to NM_144625.4 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:241929605 T>C maps to NM_144625.4 N668N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr1:241946629 C>A maps to NM_144625.4 I874I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:43638510 C>T maps to NM_001195831.1 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:122396387 G>A maps to NM_144668.4 E647E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr12:122437827 C>T maps to NM_144668.4 F1071F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:122396424 G>T maps to NM_144668.4 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:122359364 G>T maps to NM_144668.4 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA56-01A-31D-A391-08 chr12:122437839 C>T maps to NM_144668.4 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr8:124154593 A>G maps to NM_145647.3 L911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr18:54591252 C>T maps to NM_015285.2 F1209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr18:54694284 G>A maps to NM_015285.2 Q1440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr18:54361958 C>G maps to NM_015285.2 S359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr18:54629744 G>A maps to NM_015285.2 R1383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr18:54361852 C>T maps to NM_015285.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:37703083 C>G maps to NM_018034.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:37516653 C>T maps to NM_018034.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr5:37379633 C>T maps to NM_018034.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN1-01A-31D-A42E-08 chr5:37725072 G>T maps to NM_018034.2 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr15:53908140 A>G maps to NM_182758.2 D754D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr15:53908308 G>C maps to NM_182758.2 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:54003546 A>G maps to NM_182758.2 Y281Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr15:53907988 C>T maps to NM_182758.2 W805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr15:54005007 A>C maps to NM_182758.2 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr15:54008833 A>T maps to NM_182758.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr15:54003678 C>G did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr15:53907945 G>C maps to NM_182758.2 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:85186741 G>A maps to NM_032856.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr15:85191832 G>A maps to NM_032856.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr15:85189044 C>T maps to NM_032856.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr11:62603001 C>A maps to NM_018093.2 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:190333284 G>A maps to NM_032168.1 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr15:44149181 C>T maps to NM_024908.3 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:111989759 C>T maps to NM_024102.2 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:111991709 C>A maps to NM_024102.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:67288117 G>A maps to NM_024763.4 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:67288097 T>A maps to NM_024763.4 G814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:67293581 G>A maps to NM_024763.4 I675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:3547607 G>A maps to NM_017818.3 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:3548888 A>G maps to NM_017818.3 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr17:1635760 C>T maps to NM_001163809.1 Q1434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr17:1635657 G>A maps to NM_001163809.1 V1399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr17:1637094 G>C maps to NM_001163809.1 V1588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:1636081 G>A maps to NM_001163809.1 L1482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr3:52294511 G>A maps to NM_025222.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr19:12780827 G>A maps to NM_032332.3 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr19:12786389 C>T maps to NM_032332.3 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr9:140472030 G>A maps to NM_138778.2 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr9:140449837 C>T maps to NM_138778.2 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr19:33663288 T>C maps to NM_173479.3 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr19:33623140 C>T maps to NM_173479.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:33666476 G>A maps to NM_173479.3 *473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr16:703598 G>A maps to NM_145294.4 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:716289 C>T maps to NM_145294.4 F1560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr16:700001 G>A maps to NM_145294.4 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr16:712822 C>T maps to NM_145294.4 L1430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr16:715957 C>G maps to NM_145294.4 L1481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr16:700264 C>T maps to NM_145294.4 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr7:134894411 G>A maps to NM_014149.3 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr7:134893696 G>C maps to NM_014149.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:134873229 G>A maps to NM_014149.3 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr7:134891916 C>T maps to NM_014149.3 Q183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr7:134881080 C>T maps to NM_014149.3 E353E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMW-01A-11D-A42E-08 chr7:134878388 G>C maps to NM_014149.3 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr2:68358519 T>C maps to NM_138458.2 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr15:90248797 C>A maps to NM_020212.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:160139490 C>T maps to NM_001128212.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr1:27623587 C>T maps to ENST00000319394 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr1:27614208 C>T maps to ENST00000319394 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:9608063 T>C maps to NM_003390.3 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:9597433 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr11:9606821 C>T maps to NM_003390.3 R436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr11:9598140 G>A maps to NM_003390.3 K318K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr7:141414016 G>A maps to NM_001105558.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr7:141414073 G>A maps to NM_001105558.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr20:44259561 C>T maps to NM_080753.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr20:44313471 T>C maps to NM_172131.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr20:44333209 A>G maps to NM_172005.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:44098500 G>T did not map to a codon.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr20:44181844 G>A maps to NM_130896.2 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr20:44184452 C>T maps to NM_130896.2 W111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr20:44180701 G>C maps to NM_130896.2 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr17:48918136 C>G maps to NM_175575.5 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:48917452 C>T maps to NM_175575.5 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr4:6302886 G>A maps to NM_006005.3 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:6303813 C>G maps to NM_006005.3 P764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr4:6303042 C>G maps to NM_006005.3 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr4:1957528 G>A maps to NM_133335.3 K876K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr4:1902578 C>T maps to NM_133335.3 N66N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:1940245 C>G maps to NM_133335.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr4:1955245 C>G maps to NM_133335.3 S778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr4:1957745 T>A maps to NM_133335.3 V904V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr4:1976669 C>T maps to NM_133335.3 L1151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:1932435 G>A maps to NM_133335.3 Q498Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr4:1977055 C>T maps to NM_133335.3 L1184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr4:1920004 C>G maps to NM_133335.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr8:38175524 G>C maps to NM_017778.2 V629V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr8:38133859 G>C maps to NM_023034.1 P1342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr4:1985606 G>A maps to NM_005663.3 Q435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr4:1985625 C>T maps to NM_005663.3 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr4:1991498 C>T maps to NM_005663.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr4:1985772 C>T maps to NM_005663.3 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr12:56295979 C>T maps to NM_032345.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:65514280 A>G maps to NM_007191.4 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr2:175436668 C>T maps to NM_003387.4 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:175436405 G>C maps to NM_003387.4 S376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr2:175446122 C>G maps to NM_003387.4 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr17:38420869 C>T maps to NM_133264.4 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr17:38420830 C>T maps to NM_133264.4 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr17:66429696 G>A maps to NM_017983.5 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:66430740 G>A maps to NM_017983.5 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:66423332 G>A maps to NM_017983.5 Q379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:66425046 C>T maps to NM_017983.5 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr17:66446937 G>A maps to NM_017983.5 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr17:66447038 C>G did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr8:134239871 C>T maps to NM_003882.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr8:134237735 C>T maps to NM_003882.2 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr20:43348707 C>G maps to NM_003881.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr6:112375517 G>T maps to NM_198239.1 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:15535112 C>T maps to ENST00000389282 Q1559Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:15535457 C>T maps to ENST00000389282 V1522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:15535531 C>A maps to ENST00000389282 E1498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr19:15535181 T>C maps to ENST00000389282 E1536E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:68620904 G>A maps to NM_024911.6 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:68624817 G>A maps to NM_024911.6 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:68624829 G>A maps to NM_024911.6 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr12:988794 G>A maps to NM_018979.3 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:994163 C>T maps to NM_001184985.1 L1658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr12:939307 C>T maps to NM_001184985.1 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr12:922873 C>T maps to NM_001184985.1 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr12:988981 C>T maps to NM_018979.3 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:988904 C>G maps to NM_018979.3 S847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr12:1005553 C>T maps to NM_001184985.1 I2227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr12:978033 G>T maps to NM_001184985.1 E1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr9:96051799 G>C maps to ENST00000297954 L1625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr9:95947795 C>A maps to ENST00000297954 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr9:96015213 G>A maps to ENST00000297954 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr9:95947795 C>G maps to ENST00000297954 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr23:54259292 G>A did not map to a codon.
Sequencing variant TCGA-CF-A9FH-01A-11D-A38G-08 chr23:54359889 C>A did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr23:54265376 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr23:54321193 T>G did not map to a codon.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr23:54265479 G>A did not map to a codon.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr23:54225060 G>A did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:54324642 C>T did not map to a codon.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr23:54263497 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr23:54321157 C>G did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr23:54276033 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:54275758 G>C did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:54282207 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:54275656 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:54275686 G>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr23:54264804 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr23:54259391 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr17:40948535 C>T maps to NM_032387.4 T1223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr17:40936119 C>T maps to NM_032387.4 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:40933042 G>A maps to NM_032387.4 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:40939369 C>A maps to NM_032387.4 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr17:40947766 C>G maps to NM_032387.4 L1049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr12:49374387 C>T maps to NM_005430.3 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr2:219746933 C>T maps to NM_025216.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:219745725 C>T maps to NM_025216.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr12:49359915 C>A maps to NM_003394.3 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr12:49364021 G>A maps to NM_003394.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr12:49360195 G>A maps to NM_003394.3 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr12:49364040 C>T maps to NM_003394.3 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr7:120969786 G>T maps to NM_057168.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:116937714 G>A maps to NM_003391.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:113058963 C>T maps to NM_024494.2 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:113051917 C>T maps to NM_024494.2 Q12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr17:44845996 G>A maps to NM_030753.3 R253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr17:44845958 G>A maps to NM_030753.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:228210552 G>A maps to ENST00000366753 W86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:228210568 C>T maps to ENST00000366753 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr2:219736318 C>T maps to NM_006522.3 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr2:219736441 G>A maps to NM_006522.3 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr3:13896085 C>T maps to NM_004625.3 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr3:13916515 G>A maps to NM_004625.3 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr3:13896124 G>A maps to NM_004625.3 Y158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr22:46319095 C>T maps to NM_058238.2 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr22:46319101 C>T maps to NM_058238.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr5:137426629 C>T maps to NM_058244.2 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr5:137426380 G>A maps to NM_058244.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr1:228111877 T>C maps to NM_003395.2 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:44954077 G>A maps to NM_003396.1 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr17:44954071 C>T maps to NM_003396.1 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr17:44953615 G>A maps to NM_003396.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr17:44949996 G>A maps to NM_003396.1 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr17:44952648 C>T maps to NM_003396.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:7606581 C>G maps to NM_018081.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:7606645 G>T maps to NM_018081.2 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr17:7592101 G>T maps to NM_018081.2 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr8:31015038 C>T maps to NM_000553.4 V1325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:30969306 C>G maps to NM_000553.4 V755V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BR-01A-11D-A26M-08 chr8:31024661 C>A maps to NM_000553.4 V1369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr8:30999043 G>A maps to NM_000553.4 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:2769088 G>A maps to NM_020135.2 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr6:2770475 G>A maps to NM_020135.2 K379K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:25633892 C>T maps to NM_015626.8 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr12:118480754 G>A maps to ENST00000441406 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr12:118472107 T>A maps to ENST00000441406 K387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr12:118473074 C>T maps to ENST00000441406 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr12:108620795 C>T maps to ENST00000261400 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr12:108589632 C>T maps to ENST00000261400 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr12:108626556 C>T maps to ENST00000261400 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:32410604 C>G maps to NM_024426.4 *518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr11:32410687 C>T maps to NM_024426.4 Q490Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr11:32414236 G>C maps to NM_024426.4 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr6:160169272 G>C maps to NM_004906.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr6:160163118 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:34983975 G>C maps to ENST00000270288 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:34984509 C>T maps to ENST00000270288 C562C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr5:167855089 C>T maps to NM_001161661.1 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr5:167812238 C>T maps to NM_001161661.1 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr5:167833248 G>T maps to NM_001161661.1 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:167855722 C>A maps to NM_001161661.1 S644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr5:167855778 C>T maps to NM_001161661.1 Q663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr4:184129223 G>A maps to ENST00000448232 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A871-01A-11D-A34U-08 chr4:184114757 G>A maps to ENST00000448232 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr4:184182434 C>T maps to ENST00000448232 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr4:184210769 G>A maps to ENST00000448232 L1146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:10104697 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr23:10106774 C>T did not map to a codon.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr23:10090709 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr23:10106889 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr23:10098143 C>T did not map to a codon.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr23:10102469 A>T did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr23:10090762 G>C did not map to a codon.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr23:10094174 C>A did not map to a codon.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr23:10093066 C>T did not map to a codon.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr23:10102504 C>T did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr23:10058873 G>A did not map to a codon.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr23:10102571 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr23:10092307 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr23:10047803 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr23:10094306 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RM-01A-11D-A38G-08 chr23:10046914 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:10058933 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr8:87414421 C>T maps to NM_007013.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:87442958 G>T maps to NM_007013.3 G456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr16:69942717 C>G maps to NM_007014.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr16:69973021 C>T maps to NM_007014.3 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr16:69969880 C>G maps to NM_007014.3 V656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:149290705 G>A maps to NM_001168278.1 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62N-01A-11D-A30E-08 chr19:7685556 T>C did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr19:7685743 C>T maps to NM_020196.2 Q653Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr19:7690903 G>A maps to NM_020196.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:7689192 C>A maps to NM_020196.2 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SU-01A-31D-A391-08 chr19:7685537 G>A maps to NM_020196.2 H663H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr17:6674104 A>T maps to NM_017523.2 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr23:52893893 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr23:52844215 A>C did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr23:52844141 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr23:52844173 C>T did not map to a codon.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr23:52841611 T>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr3:46062509 C>G maps to NM_005283.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:31572631 G>A maps to NM_000379.3 F963F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:31587028 G>A maps to NM_000379.3 Q876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:31598299 G>A maps to NM_000379.3 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr23:2670372 C>A did not map to a codon.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr23:2729396 G>A did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr23:2670373 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr23:2692777 C>T did not map to a codon.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:123022476 G>A did not map to a codon.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr23:123020108 G>T did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr23:123040976 G>A did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:123019710 C>T did not map to a codon.
Sequencing variant TCGA-CF-A9FL-01A-11D-A38G-08 chr3:39226127 G>A maps to NM_194293.2 V1603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr3:39225688 G>A maps to NM_194293.2 L1750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr3:39228106 G>A maps to NM_194293.2 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr3:39229229 T>C maps to NM_194293.2 E569E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr3:39227495 G>A maps to NM_194293.2 P1147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr3:39226078 C>A maps to NM_194293.2 E1620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr2:168110618 C>T maps to NM_152381.5 Q3545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr2:168099888 T>C maps to NM_152381.5 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr2:168108452 A>C maps to NM_152381.5 I3517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:168106304 C>T maps to NM_152381.5 P2801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr2:168103463 G>A maps to NM_152381.5 Q1854Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr2:168103928 A>G maps to NM_152381.5 L2009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:168102693 G>T maps to NM_152381.5 E1598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:168104375 C>T maps to NM_152381.5 S2158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr2:168067297 C>A maps to NM_152381.5 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr2:167760234 G>T maps to NM_152381.5 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr2:168100850 C>T maps to NM_152381.5 F983F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr2:168105956 A>G maps to NM_152381.5 Q2685Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:168100155 C>T maps to NM_152381.5 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr2:168103445 C>T maps to NM_152381.5 L1848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr2:168115728 C>T maps to ENST00000420519 A924A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:168103797 C>T maps to NM_152381.5 Q1966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr2:168102224 C>T maps to NM_152381.5 V1441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:168105338 G>A maps to NM_152381.5 Q2479Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr2:168115749 T>A maps to ENST00000420519 G931G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr2:168103116 G>T maps to NM_152381.5 E1739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr2:168096395 C>G maps to NM_152381.5 S297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr2:168103175 G>A maps to NM_152381.5 L1758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr2:168102264 C>T maps to NM_152381.5 L1455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr2:167760087 T>C maps to NM_152381.5 H32H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr2:168105038 C>T maps to NM_152381.5 L2379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr2:168115606 G>T maps to ENST00000420519 E884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:37587303 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr23:37587043 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr22:17288834 G>C maps to NM_175878.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:56015533 C>T maps to NM_052898.1 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:56015539 C>T maps to NM_052898.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr8:56436503 C>T maps to NM_052898.1 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr8:56015488 C>T maps to NM_052898.1 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr8:6682776 G>A maps to NM_207411.4 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr8:10782177 G>A maps to NM_173683.3 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr8:10755761 C>T maps to NM_173683.3 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr20:30585203 C>T maps to NM_001011718.1 Q562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr20:30584821 C>T maps to NM_001011718.1 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr20:30584443 C>T maps to NM_001011718.1 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr20:30584635 G>A maps to NM_001011718.1 W372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr20:30585076 G>A maps to NM_001011718.1 E519E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr20:30556313 C>T maps to NM_001011718.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr20:30556184 C>T maps to NM_001011718.1 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr20:30584812 C>T maps to NM_001011718.1 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:28290196 C>T maps to NM_018053.2 Y161Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr23:100178034 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:100177841 G>A did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:100169785 A>T did not map to a codon.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr23:100177919 G>A did not map to a codon.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr23:100169833 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr23:100170025 G>A did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr3:14207073 G>C maps to NM_004628.4 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr10:111640656 G>A maps to NM_020383.3 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr10:111631598 G>A maps to NM_020383.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr23:128887211 C>G did not map to a codon.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr23:128902391 C>T did not map to a codon.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr23:128881674 G>A did not map to a codon.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr23:128880618 G>C did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:61715380 C>T maps to NM_003400.3 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr2:61724136 C>T maps to NM_003400.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr2:61721202 T>A maps to NM_003400.3 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr2:61719259 G>A maps to NM_003400.3 F599F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:21396421 G>A maps to NM_022459.4 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr13:21381665 G>A maps to NM_022459.4 Q583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr13:21370907 C>A maps to NM_022459.4 G871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr6:43541305 G>A maps to NM_020750.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr6:43498483 G>A maps to NM_020750.2 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr6:43516010 G>A maps to NM_020750.2 Q683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr6:43516070 C>A maps to NM_020750.2 E663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr6:43521205 G>C maps to NM_020750.2 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:43492226 G>C maps to NM_020750.2 L1153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr16:28137113 C>G maps to NM_015171.2 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr16:28112859 G>A maps to NM_015171.2 F1065F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:28145185 C>T maps to NM_015171.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr16:28117726 C>T maps to NM_015171.2 Q863Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr8:21840320 G>A maps to ENST00000434536 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr8:21856689 G>A maps to ENST00000434536 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr8:21827718 T>C maps to ENST00000434536 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr12:64833038 C>T maps to NM_007235.3 Q917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr1:180651500 C>T maps to NM_004736.3 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:180775196 G>C did not map to a codon.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr1:180843063 A>G maps to NM_004736.3 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr1:180794030 C>T maps to NM_004736.3 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr1:180804089 G>A maps to NM_004736.3 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr1:180832931 C>G maps to NM_004736.3 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr1:180849373 G>A maps to NM_004736.3 K657K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr19:44050238 C>T maps to NM_006297.2 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:44050096 C>T maps to NM_006297.2 Q498Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr19:44050238 C>T maps to NM_006297.2 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:44051122 G>T maps to NM_006297.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr7:152346061 C>A maps to NM_005431.1 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr14:104174928 G>A maps to NM_005432.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:104165272 G>T maps to NM_005432.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr14:104165251 G>A maps to NM_005432.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr2:216983822 C>T maps to NM_021141.3 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr3:142116295 G>T maps to NM_019001.3 Y738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr3:142122728 C>T maps to NM_019001.3 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr3:142140316 C>T did not map to a codon.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr3:142094678 G>T maps to NM_019001.3 S980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr3:142119369 G>C maps to NM_019001.3 S708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr3:142103420 G>A maps to NM_019001.3 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr20:21321375 C>T maps to NM_012255.3 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr20:21321405 C>G maps to NM_012255.3 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:74651850 G>A maps to NM_182969.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr11:74556165 C>A maps to NM_182969.1 E619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr11:74617439 G>A maps to NM_182969.1 Q275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr3:38414168 C>G maps to NM_005108.3 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:38437042 G>T maps to NM_005108.3 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr3:38408353 C>G maps to NM_005108.3 S188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr16:17352857 G>A maps to NM_022166.3 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:17211611 C>T maps to NM_022166.3 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:17228460 C>T maps to NM_022166.3 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr16:17211623 C>T maps to NM_022166.3 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:17211524 C>T maps to NM_022166.3 S845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:48434546 G>A maps to NM_022167.2 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr17:48435843 G>T maps to NM_022167.2 E740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr17:48434546 G>A maps to NM_022167.2 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr12:42631499 G>T maps to NM_001190979.1 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:102100668 T>C maps to NM_001130145.2 *505Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:102100565 G>C maps to NM_001130145.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:102098266 C>T maps to NM_001130145.2 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:33245124 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:33252625 C>T maps to NM_003680.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:33272133 T>A maps to NM_003680.3 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:32903719 G>A maps to NM_001040436.1 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr12:32903744 G>C maps to NM_001040436.1 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr12:32908746 G>C maps to NM_001040436.1 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr17:7193037 G>A maps to NM_015982.3 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr22:21984215 G>A maps to NM_001017964.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:183503989 C>T maps to NM_018023.4 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr3:183442277 A>T maps to NM_018023.4 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr3:183528369 G>T maps to NM_018023.4 *1423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr3:183515777 C>G maps to NM_018023.4 L1055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr3:183526913 G>A maps to NM_018023.4 L1372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:724560 C>A maps to NM_005433.3 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr18:756620 C>A maps to NM_005433.3 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:54343991 G>T maps to NM_018982.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:54348949 C>T did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:11034008 G>A maps to NM_024029.3 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:11034230 C>T maps to NM_024029.3 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:11038320 G>A maps to NM_024029.3 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr6:43483805 C>A maps to ENST00000506469 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr23:67741302 C>T did not map to a codon.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr19:19648239 C>T maps to NM_198537.3 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr14:75231007 G>A maps to NM_019589.2 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr14:75230696 C>T maps to NM_019589.2 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:75276131 C>A maps to NM_019589.2 S1524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr14:75265974 A>G maps to NM_019589.2 E1325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr14:75230629 C>T maps to NM_019589.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr14:75230420 C>T maps to NM_019589.2 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr14:75230876 C>T maps to NM_019589.2 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr10:27415708 C>A maps to NM_139312.1 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr10:27431369 G>A maps to NM_139312.1 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr10:27425214 G>C maps to NM_139312.1 S234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr10:27423783 G>A maps to NM_139312.1 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr10:27437903 G>A maps to NM_139312.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr10:27437956 G>A maps to NM_139312.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr22:22064976 T>C maps to NM_013313.3 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr16:30106199 C>T maps to NM_031477.4 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr11:57413862 G>A maps to NM_145008.2 C67C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr2:135739073 G>A maps to NM_025052.3 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr2:135756416 C>T maps to NM_025052.3 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr2:135739073 G>A maps to NM_025052.3 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:69188521 G>A maps to NM_001031732.2 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:112903524 C>T maps to NM_022828.3 Q1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr5:112860755 G>A maps to NM_022828.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr5:112849732 C>T maps to NM_022828.3 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr1:29068982 C>T maps to NM_016258.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:29095439 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:29069199 C>T maps to NM_016258.2 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:29069441 C>T maps to NM_016258.2 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr8:64099963 C>T maps to ENST00000339066 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr8:64100092 C>G maps to ENST00000339066 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr8:64098992 C>T maps to ENST00000339066 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr17:1268268 T>A maps to NM_006761.4 K50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr17:1268269 A>T maps to NM_006761.4 Y49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr2:9770311 C>T maps to NM_006826.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr8:101960934 G>A maps to NM_003406.3 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr14:100705713 G>T maps to NM_003403.3 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr14:100728700 C>G maps to NM_003403.3 S247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:155629591 C>T maps to ENST00000368339 V841V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr1:155638471 C>T maps to ENST00000368339 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:155630384 G>T maps to ENST00000368339 S577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr1:155629566 G>A maps to ENST00000368339 L850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:21875390 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr23:21874978 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:21875004 C>T did not map to a codon.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr17:74076413 C>T maps to NM_180990.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:74076443 C>T maps to NM_180990.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr18:72913706 C>T maps to NM_175907.4 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:174131030 C>G maps to NM_016653.2 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr2:174130882 C>G maps to NM_016653.2 S603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr7:100382357 G>A maps to ENST00000349350 L2245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr7:100364684 C>T maps to ENST00000349350 G1555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr7:100334564 C>T maps to ENST00000349350 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr7:100373014 A>G maps to ENST00000349350 L1948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:100363104 C>T maps to ENST00000349350 F1466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr7:100364723 G>C maps to ENST00000349350 L1568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr7:100392930 C>G maps to ENST00000349350 L2746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr7:100345212 G>T maps to ENST00000349350 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr7:100361664 C>T maps to ENST00000349350 H1371H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr7:100391637 C>G maps to ENST00000349350 T2661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr7:100361432 C>T maps to ENST00000349350 Q1331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr2:98340714 C>T maps to NM_001079.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr2:98341691 G>A maps to NM_001079.3 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:98349417 C>T maps to NM_001079.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr2:98340693 C>G maps to NM_001079.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr2:98340717 C>T maps to NM_001079.3 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:98349601 G>T maps to NM_001079.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr3:167023706 G>A maps to ENST00000307529 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr3:167031855 G>A maps to ENST00000307529 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr23:2406962 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:2406873 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:2408699 C>T did not map to a codon.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr23:2407128 G>C did not map to a codon.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr23:2408601 C>G did not map to a codon.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr23:2407456 T>C did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr23:2407721 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr22:50277807 G>A maps to NM_014838.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr22:50280681 C>T maps to NM_014838.2 C1124C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr22:50279760 G>A maps to NM_014838.2 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr22:50277564 G>A maps to NM_014838.2 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr22:50280474 G>A maps to NM_014838.2 S1055S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr20:56191384 G>C maps to NM_030776.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr20:56190024 C>T maps to NM_030776.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:56191453 C>T maps to NM_030776.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:101390112 G>A maps to NM_014415.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:101390033 G>A maps to NM_014415.3 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr3:101391040 G>C maps to NM_014415.3 V109V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-UY-A9PH-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr6:31867810 G>A maps to NM_181842.2 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A678-01A-11D-A30E-08 chr6:31869058 C>T maps to NM_181842.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr11:113935158 C>T maps to NM_001018011.1 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr11:113934210 C>T maps to NM_001018011.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr11:113934474 G>A maps to NM_001018011.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr1:16268727 G>C maps to ENST00000375733 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:16269162 C>T maps to ENST00000375733 V633V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr1:16269032 G>A maps to ENST00000375733 Q677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr1:16270339 G>A maps to ENST00000375733 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KW-01A-11D-A38G-08 chr3:114069541 C>T maps to NM_001164342.1 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr3:114070333 C>T maps to NM_001164342.1 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr3:114069469 G>A maps to NM_001164342.1 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr3:114070606 T>C maps to NM_001164342.1 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr6:33284381 G>A maps to NM_001145338.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:33283234 G>A maps to NM_001145338.1 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:33284429 G>C maps to NM_001145338.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr6:33284495 C>T maps to NM_001145338.1 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:33284066 G>A maps to NM_001145338.1 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr6:33283568 G>A maps to NM_001145338.1 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr6:33284342 G>A maps to NM_001145338.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr6:33283568 G>C maps to NM_001145338.1 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr6:109803085 G>A maps to NM_014797.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr14:64954554 G>A maps to NM_006977.2 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr9:125681288 G>A maps to NM_020924.2 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr11:62520866 C>T maps to NM_024784.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:36206034 G>A maps to NM_014383.1 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr19:36206115 C>T maps to NM_014383.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:119387704 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr23:119387421 C>T did not map to a codon.
Sequencing variant TCGA-E7-A5KF-01A-11D-A289-08 chr23:119387417 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr23:119387327 A>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:119387873 C>G did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:119388378 C>G did not map to a codon.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr23:119387400 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:119387501 T>C did not map to a codon.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr9:129642679 G>A maps to ENST00000319119 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:173839951 C>T maps to NM_001122770.1 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:173839956 C>T maps to NM_001122770.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:141162246 T>G maps to NM_001080412.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr3:141163250 C>G maps to NM_001080412.2 S674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr3:141163574 C>G maps to NM_001080412.2 S782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr3:141161502 C>A maps to NM_001080412.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr3:141164049 G>A maps to NM_001080412.2 R940R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MF-01A-12D-A32B-08 chr3:141164571 G>A maps to NM_001080412.2 Q1114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:141161775 G>A maps to NM_001080412.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr3:141163026 A>C maps to NM_001080412.2 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr12:57397507 G>A maps to NM_014830.2 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:57398641 G>C maps to NM_014830.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr12:57398524 G>A maps to NM_014830.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr17:7367106 C>T maps to NM_020899.3 E398E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:7365510 G>T maps to NM_020899.3 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:7369148 C>G maps to NM_020899.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:22816494 C>T maps to NM_014870.3 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:22828865 C>T maps to NM_014870.3 Q367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr1:22846689 G>A maps to NM_014870.3 P990P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:22828001 C>T maps to NM_014870.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr1:22839531 C>T maps to NM_014870.3 T859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr1:22817959 C>G maps to NM_014870.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr1:22828849 G>C maps to NM_014870.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMR-01A-31D-A42E-08 chr1:22817052 G>A maps to NM_014870.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr1:22828016 A>G maps to NM_014870.3 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:197144230 G>A maps to NM_194314.2 Q632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr1:197147642 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr9:129595391 G>T maps to NM_014007.3 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr19:59028485 T>C maps to NM_032792.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr19:59027762 C>T maps to NM_032792.2 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:59025543 C>T maps to NM_032792.2 K471K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr19:59028838 C>A maps to NM_032792.2 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr20:62421702 G>A maps to NM_025224.2 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:62421336 C>T maps to NM_025224.2 Q258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:62378297 G>A maps to NM_025224.2 F585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr20:62422017 G>A maps to NM_025224.2 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr20:62421401 G>A maps to NM_025224.2 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G0-01A-12D-A38G-08 chr20:62407301 G>A maps to NM_025224.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr20:62421738 G>A maps to NM_025224.2 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr3:42705287 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:6640689 G>A maps to NM_005341.2 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:6640683 C>T maps to NM_005341.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr1:6641235 C>T maps to NM_005341.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:6640716 C>T maps to NM_005341.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:4303907 A>T maps to NM_145291.3 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr4:4304291 C>T maps to NM_145291.3 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr4:4303793 G>A maps to NM_145291.3 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:125674273 C>T maps to NM_006626.4 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr9:125673160 G>A maps to NM_006626.4 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:4048049 G>A maps to NM_015898.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:4048229 C>T maps to NM_015898.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:4048151 G>A maps to NM_015898.2 Y451Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr19:4055074 C>T maps to NM_015898.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:154988998 C>T maps to ENST00000417934 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr1:154988171 C>T maps to ENST00000417934 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr18:45556269 C>T maps to NM_001039360.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr18:45566388 G>A maps to NM_001039360.2 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr18:45566362 G>A maps to NM_001039360.2 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:33058580 C>T maps to NM_001040441.1 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr6:33423780 C>T maps to NM_152735.3 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr6:33422948 G>A maps to NM_152735.3 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr12:56514594 G>A maps to NM_032786.1 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr12:56515545 G>A maps to NM_032786.1 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr12:56515126 C>T maps to NM_032786.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr12:56515471 G>T maps to NM_032786.1 G376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr1:203802940 G>A maps to NM_014827.4 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr1:203816717 G>A maps to NM_014827.4 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:37947424 C>T maps to NM_025079.2 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr1:37947334 C>T maps to NM_025079.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr1:37945896 G>T maps to NM_025079.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:37941261 C>T maps to NM_025079.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr23:64708912 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr23:64722818 G>C did not map to a codon.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr23:64718934 C>T did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:64722510 G>C did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:64718883 G>C did not map to a codon.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr23:64718970 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr11:110035201 G>A maps to NM_033390.1 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr11:110007974 A>G maps to NM_033390.1 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr6:149795565 C>T maps to NM_207360.2 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr6:149795652 G>A maps to NM_207360.2 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr13:46549611 C>T maps to ENST00000242848 R758R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr13:46594681 G>C maps to ENST00000242848 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr14:89029485 C>T maps to NM_024824.4 I3I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:89061435 C>T maps to NM_207662.3 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr14:89069336 C>G maps to NM_024824.4 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:88677719 C>G maps to ENST00000452588 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:88690428 C>T maps to ENST00000452588 I643I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr16:88664597 G>A maps to ENST00000452588 W258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr8:144523268 G>A maps to NM_015117.2 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:47597705 C>T maps to NM_015168.1 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:47597283 G>A maps to NM_015168.1 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr19:47572421 C>T maps to NM_015168.1 Q775Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr19:47585483 G>A maps to NM_015168.1 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:113089650 G>A maps to NM_198581.2 R1052R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr2:113089361 C>A maps to NM_198581.2 S956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:113088858 G>A maps to NM_198581.2 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr16:11850151 G>A maps to NM_014153.3 Q835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr16:11855264 A>G maps to NM_014153.3 F772F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr16:11850212 C>T maps to NM_014153.3 E814E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr16:11859380 G>A maps to NM_014153.3 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr16:11859510 G>C maps to NM_014153.3 S518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr22:41752422 C>T maps to ENST00000351589 I836I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WY-01A-11D-A22Z-08 chr22:41752380 G>A maps to ENST00000351589 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr2:113012513 G>C maps to NM_032494.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr7:138761138 G>C maps to ENST00000464606 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr7:138738727 G>A maps to ENST00000464606 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr7:138764622 G>C maps to ENST00000464606 S355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr7:138764693 T>C maps to ENST00000464606 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr7:138758619 C>T maps to ENST00000464606 W740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr7:138764923 G>A maps to ENST00000464606 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr7:138764450 G>A maps to ENST00000464606 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr7:138768691 G>A maps to ENST00000464606 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr7:129663416 G>C maps to NM_016478.3 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr7:129680854 G>C maps to NM_016478.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:129668803 G>A maps to NM_016478.3 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr7:129658504 C>G maps to NM_016478.3 *503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr23:64139076 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:64139061 C>A did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr5:132362196 C>G maps to ENST00000509437 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr1:52896985 G>C maps to NM_001009881.2 V1470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr1:52991326 G>C maps to NM_001009881.2 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:52941061 C>T maps to NM_001009881.2 K723K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr1:52941115 C>T maps to NM_001009881.2 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr1:52889674 C>T did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr23:117960325 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:117959627 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr23:117959284 G>A did not map to a codon.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr23:73524405 G>A did not map to a codon.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr23:73524500 G>T did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:73524384 G>C did not map to a codon.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr16:87457448 T>C maps to NM_015144.2 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr16:87446452 G>C maps to NM_015144.2 S488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr16:87448967 C>T maps to NM_015144.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr16:87493734 G>A maps to NM_015144.2 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr23:111698851 G>C did not map to a codon.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr23:111698706 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:111698856 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:111698392 C>G did not map to a codon.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr23:111698850 C>A did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:31819498 G>A maps to NM_016505.2 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr1:31811808 A>G maps to NM_016505.2 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:103359456 G>T did not map to a codon.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr23:103359014 C>T did not map to a codon.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr18:60217633 G>A maps to NM_017742.4 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr18:60241917 C>T maps to NM_017742.4 I868I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr18:60242454 A>T maps to NM_017742.4 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr10:81192415 C>T maps to NM_153367.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr20:278757 C>T maps to NM_033089.6 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr20:279102 G>T maps to NM_033089.6 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr20:278844 G>A maps to NM_033089.6 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr4:25351118 C>T maps to NM_024936.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr23:77913853 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr23:77912688 T>A did not map to a codon.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr23:77912559 T>A did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr23:77912674 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr23:77912860 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr9:88955937 G>A maps to NM_024617.3 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr9:88952369 C>T maps to NM_024617.3 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20X-01A-11D-A16O-08 chr9:88958023 G>T maps to NM_024617.3 S351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr9:88953751 T>G maps to NM_024617.3 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr9:88954988 A>G maps to NM_024617.3 H390H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr9:88967718 G>T maps to NM_024617.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr12:122985351 G>C maps to NM_017612.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr12:122962439 C>T maps to NM_017612.2 Q431Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr5:80600668 A>C maps to NM_032280.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:80604426 C>T maps to NM_032280.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr7:100002661 G>A maps to NM_017984.3 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr7:100007054 G>A maps to NM_017984.3 N288N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr2:207176148 C>T maps to NM_020923.1 C2299C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:207162007 G>A maps to NM_020923.1 Q33Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:207170662 G>T maps to NM_020923.1 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:207172180 G>T maps to NM_020923.1 E977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr2:207175584 G>A maps to NM_020923.1 P2111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr2:207169442 C>G maps to NM_020923.1 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr2:207172244 C>G maps to NM_020923.1 S998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr2:207172434 G>A maps to NM_020923.1 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr16:67428778 G>A maps to NM_013304.2 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr16:67434995 G>A maps to NM_013304.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr16:67428784 G>T maps to NM_013304.2 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr16:67432116 G>A maps to NM_013304.2 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr5:819657 G>A maps to NM_024786.2 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:157803262 C>T maps to NM_024630.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:158094117 C>T maps to NM_024630.2 D477D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr6:158074649 G>A maps to NM_024630.2 Q353Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BV-01A-11D-A26M-08 chr23:74698807 A>C did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:74641728 T>A did not map to a codon.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr10:99212254 C>A maps to NM_198046.1 C174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr3:195937532 G>A maps to NM_001039617.1 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr9:14674275 G>A maps to NM_178566.4 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:77605613 G>A maps to NM_174976.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:113673210 C>A maps to NM_173570.3 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr3:113677339 C>T maps to NM_173570.3 Q391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:113673023 G>A maps to NM_173570.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr11:66313209 G>A maps to NM_207340.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:45000760 G>C maps to NM_016598.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:45000793 G>A maps to NM_016598.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:44975427 G>C maps to NM_016598.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:6624734 C>A maps to NM_018106.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:57467490 G>A maps to NM_015457.2 E712E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr11:57457839 C>T maps to NM_015457.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr11:57457549 G>C maps to NM_015457.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr11:57467430 C>T maps to NM_015457.2 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr10:114203354 G>A maps to NM_022494.1 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr16:85010831 C>G did not map to a codon.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr16:85010724 G>A maps to NM_001145548.1 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr22:20131231 C>T maps to NM_013373.3 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr22:20130669 C>G maps to NM_013373.3 S506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:128963080 G>T did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr23:128947697 G>C did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr23:128948700 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:128946731 T>C did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:128957703 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:31812997 C>T maps to NM_001174096.1 F914F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr2:145147110 C>T maps to NM_014795.3 E1184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:145161506 C>T maps to NM_014795.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr2:145147515 G>A maps to NM_014795.3 H1049H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr2:145147496 G>A maps to NM_014795.3 Q1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:145157757 C>T maps to NM_014795.3 K332K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:145274902 G>A maps to NM_014795.3 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:131517772 G>A maps to NM_006336.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:131515055 G>A maps to NM_006336.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:131503881 C>A maps to NM_006336.2 E557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr9:131504958 G>A maps to NM_006336.2 Y475Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr9:131503855 G>A maps to NM_006336.2 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr8:82630459 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr8:82626197 C>T maps to NM_024699.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr7:1195097 C>T maps to ENST00000401903 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr2:220073013 T>G maps to NM_138802.1 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:38084504 G>A maps to NM_021943.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr9:74971942 G>A maps to ENST00000437241 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr8:135615034 G>T maps to NM_020863.3 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr8:135524802 G>C maps to NM_020863.3 L1092L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr8:135669837 T>C maps to NM_020863.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr8:135614908 C>T maps to NM_020863.3 K351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:72026080 G>A maps to NM_144982.4 Q1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr12:72030287 A>G maps to NM_144982.4 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr12:72021643 G>A maps to NM_144982.4 Y1339Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr16:72821608 G>A maps to NM_006885.3 G3522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr16:72991866 G>A maps to NM_006885.3 F726F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr16:72984604 G>A maps to NM_006885.3 T993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr16:72821413 C>T maps to NM_006885.3 S3587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr16:72821497 C>G maps to NM_006885.3 T3559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr16:72923774 G>C maps to NM_006885.3 L1101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr16:72992823 G>A maps to NM_006885.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:72828401 C>A maps to NM_006885.3 E2727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:72993468 C>T maps to NM_006885.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr16:72992973 G>C maps to NM_006885.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr16:72829053 G>C maps to NM_006885.3 L2509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5ND-01A-11D-A26M-08 chr16:72829004 G>A maps to NM_006885.3 Q2526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr16:72829206 C>T maps to NM_006885.3 E2458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr16:72821596 G>A maps to NM_006885.3 G3526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr16:72992973 G>A maps to NM_006885.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr16:72831192 G>T maps to NM_006885.3 L1796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr16:72832606 G>C maps to NM_006885.3 S1325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr16:72827193 G>A maps to NM_006885.3 L3129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr16:72829013 G>A maps to NM_006885.3 L2523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:72822747 C>A did not map to a codon.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr8:77776626 C>T maps to NM_024721.4 C3559C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr8:77776410 T>C maps to NM_024721.4 V3487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr8:77764239 C>T maps to NM_024721.4 Q1695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:77618761 C>G maps to NM_024721.4 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:77776626 C>T maps to NM_024721.4 C3559C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr8:77776245 G>A maps to NM_024721.4 L3432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr8:77618233 G>A maps to NM_024721.4 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr8:77618659 C>A maps to NM_024721.4 A779A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr8:77766228 C>T maps to NM_024721.4 Q2358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BZ-01A-11D-A289-08 chr8:77763389 G>A maps to NM_024721.4 K1411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr8:77766596 G>A maps to NM_024721.4 T2480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr8:77763531 C>T maps to NM_024721.4 L1459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr8:77616898 C>T maps to NM_024721.4 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMF-01A-21D-A42E-08 chr8:77619877 C>T maps to NM_024721.4 I896I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr8:77767781 C>T maps to NM_024721.4 F2875F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr15:42736436 C>T maps to NM_022473.1 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr19:44832113 A>T maps to ENST00000412927 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr19:44832109 G>A maps to ENST00000412927 Q751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr19:44832185 G>A maps to ENST00000412927 V725V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:36851364 C>G maps to NM_020917.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr18:5290904 C>T maps to NM_003409.3 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:178359070 C>T maps to NM_030613.2 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:57058945 C>T maps to NM_020828.1 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr19:57066759 A>G maps to NM_020828.1 *869W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr17:4995010 C>G maps to NM_153018.2 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr19:38126660 G>A maps to NM_014898.2 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:39897561 C>T maps to NM_003407.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr14:69257105 G>C maps to NM_004926.2 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:69256369 G>C maps to NM_004926.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr14:69256991 G>T maps to NM_004926.2 S92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr14:69256747 G>T maps to NM_004926.2 C173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6T-01A-11D-A391-08 chr14:69259600 T>A maps to NM_004926.2 K19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr2:43452288 C>A maps to NM_006887.4 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:43451535 G>A maps to NM_006887.4 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:43451823 G>A maps to NM_006887.4 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:43452197 C>A maps to NM_006887.4 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:43452312 C>T maps to NM_006887.4 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr2:43452596 C>A maps to NM_006887.4 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:115805728 G>C maps to NM_003408.1 S390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr9:115818938 C>T maps to NM_003408.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr9:115806038 G>A maps to NM_003408.1 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr9:115806345 C>T maps to NM_003408.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr9:115805097 G>T maps to NM_003408.1 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr9:115805026 G>C maps to NM_003408.1 S624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B0-01A-11D-A31L-08 chr4:188924122 G>A maps to NM_174900.3 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr4:188924536 G>A maps to NM_174900.3 Q192Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:29640795 G>T maps to NM_001109809.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr6:29640987 G>A maps to NM_001109809.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr6:29640751 G>C maps to NM_001109809.2 S379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr6:29641013 C>A maps to NM_001109809.2 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr6:29643164 G>C maps to NM_001109809.2 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr20:50769824 G>C maps to NM_018197.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr20:50768753 C>T maps to NM_018197.2 Q659Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr20:50713924 G>A maps to NM_199427.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr19:36898789 C>G maps to NM_133466.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr16:68598450 G>A maps to NM_133458.2 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:58384282 A>G maps to NM_053023.4 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr11:58352327 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr11:58377336 T>A maps to NM_053023.4 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:64855480 C>T maps to NM_006782.3 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr11:64852678 G>A maps to NM_006782.3 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr16:88601197 G>A maps to NM_153813.2 P944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:88594546 G>T maps to NM_153813.2 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr8:106573709 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr8:106813557 C>T maps to NM_012082.3 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr8:106815511 C>T maps to NM_012082.3 Q1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr23:24225884 C>A did not map to a codon.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr23:24190907 G>C did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr23:24227092 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:24197770 C>T did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:24229409 G>C did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:24197516 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:24229188 T>C did not map to a codon.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr23:24229191 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr24:2829684 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr24:2847292 C>T did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr24:2844835 G>T did not map to a codon.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr24:2846007 G>T did not map to a codon.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr24:2847695 C>A did not map to a codon.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr24:2847297 C>T did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr24:2847549 C>G did not map to a codon.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr14:73460021 G>A maps to NM_021260.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr14:73460036 G>A maps to NM_021260.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr14:73444930 C>T maps to NM_021260.2 E477E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr14:73460036 G>A maps to NM_021260.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr14:73440853 G>T maps to NM_021260.2 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr14:73459853 C>T maps to NM_021260.2 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:79734014 C>G maps to NM_014733.3 S504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr5:79743931 C>T maps to NM_014733.3 Q938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr5:79751509 G>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr5:79768641 C>T maps to NM_014733.3 Q1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr5:79732689 C>T maps to NM_014733.3 C62C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr15:41105032 G>A maps to NM_001077268.1 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr15:41105569 T>C maps to NM_001077268.1 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr15:41099846 A>G maps to NM_001077268.1 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr15:41100002 G>A maps to NM_001077268.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:15124020 G>T maps to NM_022340.2 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr3:15137582 G>C maps to NM_022340.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr14:68251881 G>C maps to NM_015346.3 G1139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr14:68273294 C>G maps to NM_015346.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr14:68250040 C>T maps to NM_015346.3 P1276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr14:68257361 C>T maps to NM_015346.3 A894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr14:68233023 G>A maps to NM_015346.3 D1977D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr14:68228127 C>T maps to NM_015346.3 V2181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr14:68233026 C>T maps to NM_015346.3 T1976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SU-01A-31D-A391-08 chr14:68260449 G>T maps to NM_015346.3 R810R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMW-01A-11D-A42E-08 chr14:68229478 C>T maps to NM_015346.3 V2023V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr14:68257478 C>T maps to NM_015346.3 T855T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr10:99517058 G>A maps to NM_001002261.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr4:2273141 C>G did not map to a codon.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr4:2306150 G>C maps to NM_020972.2 S639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr4:2306647 G>A maps to NM_020972.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr4:2272526 C>T maps to NM_020972.2 V863V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:2273489 C>T maps to NM_020972.2 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr4:2306842 C>A maps to NM_020972.2 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:52704804 C>T maps to NM_004799.2 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:52705107 C>T maps to NM_004799.2 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:52805845 G>A maps to NM_004799.2 V1294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:52705014 C>T maps to NM_004799.2 V642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr1:52800414 C>T maps to NM_004799.2 Y1215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr1:52704315 G>A maps to NM_004799.2 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:52704087 C>G maps to NM_004799.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr16:2882134 C>A maps to NM_145252.2 S201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:62340318 G>A maps to NM_032527.4 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr20:62340258 G>A maps to NM_032527.4 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr20:62366841 G>A maps to NM_032527.4 Q461Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:124266209 C>A maps to NM_007222.3 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr8:124267127 C>T maps to NM_007222.3 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr8:124267735 G>A maps to NM_007222.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr8:123965511 G>T maps to NM_014943.3 E588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr8:123964019 G>A maps to NM_014943.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr20:39832520 C>A maps to NM_015035.3 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:39832341 G>A maps to NM_015035.3 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr3:147127910 C>T maps to NM_003412.3 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr3:147128303 G>A maps to NM_003412.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6ME-01A-22D-A32B-08 chr3:147128792 C>A maps to NM_003412.3 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr3:147128321 C>G maps to NM_003412.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr3:147128780 C>T maps to NM_003412.3 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr3:147131157 G>T maps to NM_003412.3 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr13:100637716 G>A maps to NM_007129.2 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr13:100637332 G>A maps to NM_007129.2 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr23:136651209 C>T did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr23:136649815 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr23:136651210 G>A did not map to a codon.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr23:136649665 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr23:136649614 G>C did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr3:147108797 C>T maps to NM_001168379.1 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr13:100617663 G>A maps to NM_033132.3 Y653Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr13:100622441 G>C maps to NM_033132.3 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr13:100622423 G>A maps to NM_033132.3 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr19:57286538 G>C maps to NM_001146326.1 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:57286772 C>T maps to NM_001146326.1 E289E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:57293483 C>A maps to NM_001146326.1 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:57286544 G>A maps to NM_001146326.1 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:57646566 G>A maps to NM_052882.1 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr19:57648316 G>A maps to NM_052882.1 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr19:57646840 G>A maps to NM_052882.1 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr19:57646980 G>A maps to NM_052882.1 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:99631036 G>A maps to NM_003439.1 E303E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr7:99631579 G>A maps to NM_003439.1 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr16:25251865 C>A maps to NM_001012981.4 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr16:25268076 C>T maps to NM_001012981.4 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr16:25258601 G>A maps to NM_001012981.4 Y305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr16:25255133 T>A maps to NM_001012981.4 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr6:28333832 G>A maps to NM_024493.2 W463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr6:28333424 C>G maps to NM_024493.2 S327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr6:28214834 G>C maps to NM_019110.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:99123931 C>T maps to NM_014569.3 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr7:99103870 C>T maps to NM_014569.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr7:99103921 G>A maps to NM_014569.3 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr7:99129155 G>T maps to NM_014569.3 E602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr7:99123463 C>T maps to NM_014569.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr7:99123475 G>A maps to NM_014569.3 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr23:101138729 A>C did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr23:101138750 C>T did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr23:101141648 A>G did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr23:101153124 A>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:101138779 T>A did not map to a codon.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr23:101152961 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr5:140085339 G>A maps to NM_144723.1 *200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr8:40532280 C>T maps to NM_024645.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr8:40438738 G>A maps to NM_024645.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr22:30136681 G>A maps to NM_019103.2 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr10:81037043 C>G maps to NM_020338.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:81061874 C>T maps to NM_020338.3 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr10:81070879 C>G maps to NM_020338.3 S1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr10:81050723 G>A maps to NM_020338.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr10:81049570 G>A maps to NM_020338.3 Q155Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr10:81051983 C>T maps to NM_020338.3 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr10:81065868 A>G maps to NM_020338.3 E812E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr10:81063877 C>T maps to NM_020338.3 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr7:44796035 C>T maps to NM_031449.3 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr7:44804046 C>T maps to NM_031449.3 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr7:44804951 C>T maps to NM_031449.3 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:44804987 C>A maps to NM_031449.3 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr1:40735777 G>A maps to NM_005857.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr1:35579713 A>C maps to NM_024772.3 V761V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:35579296 C>T maps to NM_024772.3 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:35579263 C>T maps to NM_024772.3 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr1:35570218 C>G maps to NM_024772.3 S219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr13:20611003 C>T maps to NM_001190965.1 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr13:20635275 T>G maps to NM_001190965.1 V941V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr23:70471084 C>A did not map to a codon.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr23:70470409 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr23:70465550 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:70471042 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr23:70470473 G>C did not map to a codon.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr23:70472590 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:70471042 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:70471051 C>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:70468609 C>G did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:70462850 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:70464169 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:70472881 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R1-01A-11D-A391-08 chr23:70465901 G>C did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr23:70467263 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:70470558 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr23:70468613 G>A did not map to a codon.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr1:35853066 C>T maps to NM_005095.2 Q709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:35851046 C>G maps to NM_005095.2 S525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr1:35824750 C>A maps to NM_005095.2 S104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr1:35836215 C>G maps to NM_005095.2 S390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr1:35873660 G>A maps to NM_005095.2 L1283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr1:35862171 C>T maps to NM_005095.2 P977P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:20425495 A>G maps to NM_001142684.1 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr13:20411690 A>G maps to NM_001039650.2 D381D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr1:35480459 C>A maps to NM_007167.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:35485179 G>A maps to NM_007167.3 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:35476589 C>T maps to NM_007167.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr1:35470788 G>C maps to NM_007167.3 S633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr3:50379129 C>T maps to NM_015896.2 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:50379108 C>T maps to NM_015896.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr3:50379287 C>T maps to NM_015896.2 Q358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr10:292744 C>G maps to NM_006624.4 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr17:4644987 C>G maps to NM_001136046.1 S235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr10:75184442 G>C maps to NM_001024593.1 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr10:75185671 T>A maps to NM_001024593.1 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr10:75185860 C>T maps to NM_001024593.1 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr20:45850113 G>A maps to ENST00000471951 Q1091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr20:45865138 G>C maps to ENST00000471951 V930V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr20:45853153 G>A maps to ENST00000471951 I1025I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr20:45912356 T>C maps to ENST00000471951 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:45850057 C>A maps to ENST00000471951 G1109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr20:45920580 C>A maps to ENST00000471951 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr20:45874930 G>C maps to ENST00000471951 S703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr20:45867644 G>C maps to ENST00000471951 S842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:133732755 C>T maps to NM_015394.4 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr12:133732510 C>T maps to NM_015394.4 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr12:133733325 C>T maps to NM_015394.4 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R9-01A-11D-A38G-08 chr12:133732598 C>G maps to NM_015394.4 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr19:19790109 C>A maps to NM_033204.2 C104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr7:64166774 G>A maps to NM_016220.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr7:64166947 C>G maps to NM_016220.3 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:64168349 A>G maps to NM_016220.3 E556E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr7:64167068 G>A maps to NM_016220.3 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr7:64167871 C>G maps to NM_016220.3 S397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:6730898 G>A maps to ENST00000330442 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:6732257 G>A maps to ENST00000330442 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:6730699 G>A maps to ENST00000330442 R682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr7:6730541 G>A maps to ENST00000330442 N734N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr7:6731445 G>C maps to ENST00000330442 S433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr7:6730880 G>C maps to ENST00000330442 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A766-01A-11D-A32B-08 chr7:6731372 C>T maps to ENST00000330442 Q457Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr7:6731480 C>T maps to ENST00000330442 Q421Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr7:6732257 G>A maps to ENST00000330442 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:9677728 G>A maps to NM_001008727.2 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:9676898 G>C maps to NM_001008727.2 S297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:247323034 G>C maps to NM_003431.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr1:247319960 C>T maps to NM_003431.2 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:43161884 A>G maps to ENST00000509156 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AB-01B-12D-A289-08 chr5:43122224 T>C maps to ENST00000509156 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:43161483 G>T maps to ENST00000509156 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:58944737 G>C maps to NM_003433.3 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr20:18297182 C>G maps to ENST00000401790 S565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:18286393 C>T maps to ENST00000401790 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr20:18296433 C>T maps to ENST00000401790 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr20:18297079 C>T maps to ENST00000401790 R531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr20:18297014 C>G maps to ENST00000401790 S509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr19:58132284 G>C maps to NM_003435.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr19:58578688 C>T maps to NM_007134.1 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr19:58574892 C>T maps to NM_007134.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr19:58578625 C>A maps to NM_007134.1 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr19:58578379 A>G maps to NM_007134.1 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr19:58579129 C>T maps to NM_007134.1 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr19:58579138 G>C maps to NM_007134.1 R453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:12296679 C>G maps to NM_003437.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:12298626 T>C maps to NM_003437.3 C478C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr7:64292294 T>C maps to ENST00000307355 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr7:64291895 G>A maps to ENST00000307355 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr19:19822820 T>C maps to NM_021030.2 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:19822553 G>A maps to NM_021030.2 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr4:338187 G>A maps to NM_003441.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:366776 C>G maps to NM_003441.2 S184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr4:367280 C>G maps to NM_003441.2 S352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr2:219514051 G>A maps to NM_001105537.1 C193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr2:219503171 G>A maps to NM_001105537.1 Q1652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr2:219507086 G>A maps to NM_001105537.1 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr2:219508868 C>T maps to NM_001105537.1 E790E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr2:219507881 C>G maps to NM_001105537.1 L1119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr11:9522677 G>T maps to NM_003442.5 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:36727470 T>G maps to NM_007145.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:36728008 C>T maps to NM_007145.2 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr19:36727427 C>G maps to NM_007145.2 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr19:36727605 T>C maps to NM_007145.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:124952080 G>A maps to NM_021964.2 Q497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:58213956 G>A maps to NM_001085384.1 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr19:58213086 C>T maps to NM_001085384.1 E410E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr19:58213187 T>A maps to NM_001085384.1 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:47270103 G>A did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:47269689 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr23:47272749 G>C did not map to a codon.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr8:146157800 C>T maps to NM_006958.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr8:146156420 T>A maps to NM_006958.2 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42F-01A-11D-A23U-08 chr8:146157490 G>A maps to NM_006958.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr8:146157788 C>T maps to NM_006958.2 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr8:146156408 G>A maps to NM_006958.2 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:146156261 G>A maps to NM_006958.2 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr8:146157800 C>T maps to NM_006958.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr8:146171545 G>C maps to NM_006958.2 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr8:146157423 G>T maps to NM_006958.2 S250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr19:53572487 G>T maps to NM_001102603.1 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:53573393 G>A maps to NM_001102603.1 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr19:53577474 C>T maps to NM_001102603.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr6:28053306 G>T maps to NM_003447.3 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:44612225 C>T maps to NM_018651.2 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr3:44611672 T>C maps to NM_018651.2 Y357Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr9:97055283 C>T maps to NM_194320.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:57932475 C>G maps to NM_006959.2 S539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6S-01A-21D-A391-08 chr19:57932314 G>A maps to NM_006959.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr16:3452306 G>A maps to NM_003450.2 E101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr19:52091119 C>T maps to NM_007147.2 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr19:52090801 C>G maps to NM_007147.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:52090204 G>A maps to NM_007147.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr19:52090204 G>C maps to NM_007147.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr19:9492323 G>C maps to NM_001172651.1 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr19:44981931 G>A maps to NM_013256.3 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:44981163 G>A maps to NM_013256.3 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr23:47842406 G>A did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr23:47836894 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr23:47842711 C>T did not map to a codon.
Sequencing variant TCGA-4Z-AA7Y-01A-11D-A391-08 chr6:27419942 C>T maps to NM_007149.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr6:27425077 T>A maps to NM_007149.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr6:27419546 C>T maps to NM_007149.2 Q597Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:152137986 C>T did not map to a codon.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr23:152128413 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr23:152128421 G>T did not map to a codon.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr23:152139013 G>T did not map to a codon.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr9:104170244 T>A maps to NM_003452.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr9:104171808 C>T maps to NM_003452.2 Q587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr9:104171828 G>A maps to NM_003452.2 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr9:104171252 A>G maps to NM_003452.2 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr16:71509743 G>A maps to NM_006961.3 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:28121158 A>G maps to NM_006298.2 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr6:28121656 C>T maps to NM_006298.2 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr11:3380509 T>C maps to NM_001130520.1 K576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr11:3380677 C>T maps to NM_001130520.1 K520K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:3380509 T>C maps to NM_001130520.1 K576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr3:44685244 G>T maps to NM_006991.3 E875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:44683587 G>A maps to NM_006991.3 K322K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr2:95847682 T>C maps to ENST00000453539 Y383Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr16:3282847 C>T maps to NM_198088.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:3273996 C>T maps to NM_198088.2 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:123597520 C>T maps to NM_003455.2 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr11:123598841 C>T maps to NM_003455.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA83-01A-11D-A391-08 chr19:22171636 C>T maps to NM_007153.3 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:22156368 T>C maps to NM_007153.3 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr19:22154531 C>A maps to NM_007153.3 E1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:22156690 G>C maps to NM_007153.3 S382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:22155222 T>C maps to NM_007153.3 K871K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:22157442 A>G maps to NM_007153.3 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr19:22154794 G>C maps to NM_007153.3 S1014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr7:148947563 C>T maps to NM_012256.3 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr7:148951223 C>T maps to NM_012256.3 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr7:148951298 C>T maps to NM_012256.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:3191254 C>T maps to NM_001134655.1 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr11:6977008 G>A maps to NM_013250.2 W267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr11:6953673 G>A maps to NM_013250.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr20:52199146 G>A maps to NM_006526.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr20:52188371 G>A maps to NM_006526.2 Q1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr20:52199197 G>C maps to NM_006526.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3F-01A-12D-A42E-08 chr20:52193385 G>C maps to NM_006526.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr20:52192656 G>A maps to NM_006526.2 I882I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr20:52198582 C>T maps to NM_006526.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr20:52192920 C>T maps to NM_006526.2 Q794Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:45499095 C>T maps to NM_006963.4 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr10:45499193 C>T maps to NM_006963.4 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:44537160 C>G maps to NM_001129996.1 S485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:44571039 C>T maps to NM_013361.4 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr19:44570882 C>G maps to NM_013361.4 S301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:44571218 C>G maps to NM_013361.4 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:44571288 G>A maps to NM_013361.4 K436K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr19:44611291 C>T maps to NM_013398.2 Q327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A76B-01A-11D-A32B-08 chr19:44611953 G>A maps to NM_013398.2 K547K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr19:44612110 G>T maps to NM_013398.2 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:44636768 A>T maps to NM_013362.2 K668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:44676254 C>T maps to NM_001032372.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A763-01A-11D-A32B-08 chr19:44679999 A>G maps to NM_001032372.1 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr19:44739863 G>A maps to NM_182490.1 Q427Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:44933650 G>A maps to NM_014518.2 C435C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:44933731 G>A maps to NM_014518.2 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr19:44936520 G>A maps to NM_014518.2 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:44936419 G>C maps to NM_014518.2 S72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OF-01A-11D-A26M-08 chr19:44934151 G>A maps to NM_014518.2 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr16:71482892 G>A maps to NM_145911.1 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr16:71482808 G>A maps to NM_145911.1 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:71482034 G>C maps to NM_145911.1 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:44514436 G>A maps to NM_006300.3 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr17:5009119 C>G maps to NM_014519.2 *445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:5009424 G>A maps to NM_014519.2 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:44778141 G>A maps to NM_181756.1 Q443Q. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FD-A62P-01A-32D-A30E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr19:44777397 G>A maps to NM_181756.1 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:44661582 C>T maps to NM_006630.2 Q472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr19:44792603 G>A maps to NM_004234.4 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:44791406 G>A maps to NM_004234.4 I727I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr19:44793182 C>T maps to NM_004234.4 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr19:44791823 G>A maps to NM_004234.4 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:44791463 C>T maps to NM_004234.4 E708E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr18:74611104 G>A maps to NM_007345.3 K605K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr18:74587571 C>T maps to NM_007345.3 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr18:74583655 G>C did not map to a codon.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr18:74639255 G>A maps to NM_007345.3 Q1397Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I3-01A-11D-A31L-08 chr18:74639026 G>A maps to NM_007345.3 G1352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr18:74617144 C>T maps to NM_007345.3 Q689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr18:74580690 G>A maps to NM_007345.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr18:74580639 G>C did not map to a codon.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr18:74672698 G>A maps to NM_007345.3 V1767V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr18:74639138 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:244218533 G>A maps to NM_205768.2 Q486Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr10:38121958 G>A maps to NM_021045.1 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr10:38121104 G>C maps to NM_021045.1 S393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr10:38121010 G>C maps to NM_021045.1 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr10:38121295 C>T maps to NM_021045.1 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr10:38120936 G>C maps to NM_021045.1 S449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr10:38241660 C>T maps to NM_145011.2 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr8:146108081 C>G maps to NM_021061.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr8:146107370 G>A maps to NM_021061.3 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr8:146115408 G>C maps to NM_021061.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr8:146107412 G>A maps to NM_021061.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr8:145979131 C>T maps to NM_138367.1 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42P-01A-11D-A23U-08 chr8:145948116 G>A maps to NM_138367.1 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr8:145947522 G>A maps to NM_138367.1 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr19:20003365 C>G maps to NM_021047.2 S437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:20003060 A>T maps to ENST00000427401 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:24310133 C>T maps to NM_203282.2 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:24309977 T>C maps to NM_203282.2 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr19:24309553 C>G maps to NM_203282.2 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:58452321 G>A maps to NM_005773.2 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:58452861 A>G maps to NM_005773.2 H438H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:58453104 C>T maps to NM_005773.2 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr19:58455311 T>G maps to NM_005773.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:58453881 G>C maps to NM_005773.2 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:22255684 G>A maps to NM_033468.2 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr19:22256298 C>T maps to NM_033468.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr19:22271464 C>T maps to NM_033468.2 Q305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr19:22272042 C>T maps to NM_033468.2 N497N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr19:22271789 C>G maps to NM_033468.2 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr19:22271841 C>G maps to NM_033468.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43S-01A-21D-A23U-08 chr11:116649763 C>T maps to NM_003904.3 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5P-01A-11D-A391-08 chr11:116652909 C>T maps to NM_003904.3 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7N-01A-11D-A391-08 chr16:3339454 C>T maps to NM_005741.4 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:3339454 C>T maps to NM_005741.4 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr16:3339742 G>T maps to NM_005741.4 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr16:3339567 G>A maps to NM_005741.4 E354E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr16:3339930 C>G maps to NM_005741.4 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr16:3339612 G>A maps to NM_005741.4 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:57703292 G>A maps to NM_003417.4 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:9526414 G>T maps to NM_006631.2 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr16:31895945 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr16:31927167 C>G maps to NM_003414.4 S533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:64377988 G>T maps to NM_021148.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr7:64363778 C>T maps to NM_021148.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr19:58724433 C>A maps to NM_133502.1 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr19:58723824 G>A maps to NM_133502.1 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:58718507 G>A maps to NM_133502.1 Q226Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr23:152612887 C>T did not map to a codon.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr23:152612685 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr23:152612854 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr23:152612275 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr16:89788954 C>T maps to NM_001113525.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:89789203 C>T maps to NM_001113525.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr16:89800435 C>T maps to NM_001113525.1 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:89799708 G>C did not map to a codon.
Sequencing variant TCGA-K4-A4AC-01A-21D-A26M-08 chr16:89788996 G>A maps to NM_001113525.1 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr7:111970159 G>A maps to NM_021994.2 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr7:111980948 G>A maps to NM_021994.2 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr7:111981065 G>A maps to NM_021994.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:53303273 C>T maps to NM_006969.3 K608K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:53303585 G>A maps to NM_006969.3 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr19:53304191 T>C maps to NM_006969.3 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr19:53304918 G>C maps to NM_006969.3 S60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr19:53303201 C>T maps to NM_006969.3 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr22:22869858 C>T maps to NM_080740.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr22:22869054 G>A maps to NM_080740.3 C300C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr23:129370576 G>C did not map to a codon.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr23:129361726 C>G did not map to a codon.
Sequencing variant TCGA-XF-A9SL-01A-11D-A391-08 chr23:129339309 G>C did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:56981643 G>C maps to NM_017661.2 S175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr15:56950641 C>T maps to NM_017661.2 K679K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr15:56924103 G>A maps to NM_017661.2 H844H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:200377313 G>C maps to NM_012482.3 S507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr7:148895585 G>A maps to NM_003575.2 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:148921657 C>G maps to NM_003575.2 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr7:148895471 C>T maps to NM_003575.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr19:44352540 G>A maps to NM_181845.1 E596E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr19:44351391 G>T maps to NM_181845.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:44590806 C>T maps to NM_001037813.2 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr19:44891095 G>A maps to NM_152354.3 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:44896513 G>A maps to NM_152354.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:44890644 C>A maps to NM_152354.3 E588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:44891095 G>A maps to NM_152354.3 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:44891131 C>T maps to NM_152354.3 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr17:15620574 C>T maps to NM_020652.2 Q513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr17:18565278 G>A maps to NM_001145045.1 Q514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:18565288 G>A maps to NM_001145045.1 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B0-01A-11D-A31L-08 chr17:18565372 A>G maps to NM_001145045.1 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr17:18566062 G>C maps to NM_001145045.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:16466490 C>G maps to NM_020653.2 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr17:16455630 G>A maps to NM_020653.2 Q609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr17:16455430 G>A maps to NM_020653.2 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr6:87865441 G>T maps to NM_015021.1 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:87970339 C>G maps to NM_015021.1 P2331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr6:87970066 C>T maps to NM_015021.1 D2240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:87966209 G>T maps to NM_015021.1 E955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:87967577 G>T maps to NM_015021.1 E1411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr6:87967336 C>T maps to NM_015021.1 F1330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr6:87943113 C>T maps to NM_015021.1 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr6:87966837 C>G maps to NM_015021.1 S1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr21:43413916 C>T maps to NM_020727.4 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr21:43412608 G>A maps to NM_020727.4 D532D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr21:43413853 G>A maps to NM_020727.4 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr21:43414180 G>A maps to NM_020727.4 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr21:43412800 C>T maps to NM_020727.4 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr21:43412265 G>A maps to NM_020727.4 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr19:45575215 C>A maps to NM_145288.1 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr19:45574924 G>A maps to NM_145288.1 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr7:99673191 C>T maps to NM_032924.3 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA53-01A-11D-A391-08 chr7:99669395 G>A maps to NM_032924.3 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:35435144 G>A maps to NM_001099438.1 E426E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr5:150275798 G>A maps to NM_001172831.1 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:35175769 G>A maps to ENST00000221282 Q355Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:35175907 C>T maps to ENST00000221282 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr6:28967309 G>A maps to NM_001010877.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr6:28964083 G>C maps to NM_001010877.2 S232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:9271031 C>T maps to NM_020933.4 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr6:43305864 A>T maps to NM_014345.2 A1957A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr6:43323835 G>C maps to NM_014345.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:43323778 C>T maps to NM_014345.2 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr6:43325118 G>A maps to NM_014345.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R0-01A-11D-A38G-08 chr6:43323421 G>A maps to NM_014345.2 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr6:43307535 G>C maps to NM_014345.2 L1400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A677-01A-11D-A30E-08 chr16:58031776 G>A maps to NM_020807.1 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:53383881 G>A maps to NM_207333.2 C499C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:53384364 G>A maps to NM_207333.2 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr19:53384400 C>T maps to NM_207333.2 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr19:53384082 C>T maps to NM_207333.2 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr19:53384991 C>T maps to NM_207333.2 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr19:53383940 G>A maps to NM_207333.2 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr19:53383916 G>A maps to NM_207333.2 Q488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr19:53432461 G>A maps to NM_203307.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:53432346 G>A maps to NM_203307.2 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr6:28297175 G>A maps to NM_030899.4 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr6:28297139 C>A maps to NM_030899.4 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr19:58982419 G>A maps to NM_014347.2 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr19:58966704 C>T maps to NM_207395.2 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr19:58966784 C>T maps to NM_207395.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr1:90473224 G>A maps to NM_182976.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr1:90463713 G>C did not map to a codon.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr19:58639721 G>A maps to NM_024620.3 N383N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr4:142147921 G>A maps to NM_014487.4 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr4:142153686 C>T maps to NM_014487.4 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr19:54074949 G>A maps to NM_001079907.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr19:54081037 G>A maps to NM_001079907.1 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr19:14830019 C>T maps to NM_032433.2 F627F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr19:14817515 C>T maps to NM_032433.2 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr19:14805829 C>T maps to NM_032433.2 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A764-01A-11D-A34U-08 chr19:14828479 C>T maps to NM_032433.2 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:45130354 C>T maps to NM_018102.3 E541E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr20:44578440 G>A maps to NM_022095.3 Q1223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr20:44580905 G>A maps to NM_022095.3 I1023I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATQ-01A-11D-A391-08 chr20:44582455 C>T maps to NM_022095.3 E858E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr20:44592576 C>T maps to NM_022095.3 E385E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr20:44586516 G>C maps to NM_022095.3 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr20:44577851 G>T maps to NM_022095.3 V1286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr20:44592114 G>C maps to NM_022095.3 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr20:44598195 G>A maps to NM_022095.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:25657488 C>T maps to NM_015655.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr20:25666701 C>T maps to NM_015655.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr20:25657158 C>T maps to NM_015655.2 Q255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr20:25656192 G>A maps to NM_015655.2 C577C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr20:25656895 G>C maps to NM_015655.2 S343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr20:25666734 G>A maps to NM_015655.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr10:38344795 G>T maps to NM_006954.1 E582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr10:38344683 G>A maps to NM_006954.1 Q544Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr10:38343585 C>T maps to NM_006954.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr10:38344083 C>T maps to NM_006954.1 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr10:38345343 C>G maps to NM_006954.1 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr10:43088105 G>A maps to NM_006955.1 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:43088105 G>A maps to NM_006955.1 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr10:43089799 G>A maps to NM_006955.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr10:43088840 A>G maps to NM_006955.1 H519H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr10:43088095 G>A maps to NM_006955.1 Q768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr10:43088813 A>T maps to NM_006955.1 Y528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:43089325 G>A maps to NM_006955.1 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr10:43088861 G>A maps to NM_006955.1 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7N-01A-11D-A391-08 chr20:32354702 C>T maps to ENST00000375200 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr20:32346549 C>G maps to ENST00000375200 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr20:32336847 G>A maps to ENST00000375200 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:32379154 G>A maps to ENST00000375200 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr20:32378875 G>A maps to ENST00000375200 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr20:32349814 G>A maps to ENST00000375200 Q392Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr20:32379085 G>A maps to ENST00000375200 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr20:32332957 G>T maps to ENST00000375200 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr20:32346561 C>T maps to ENST00000375200 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr20:2463827 G>A maps to NM_024325.4 I593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr20:2465218 G>A maps to NM_024325.4 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr20:2463998 G>A maps to NM_024325.4 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:37369174 C>T maps to NM_003419.3 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:37367914 C>T maps to NM_003419.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr5:176468220 A>T maps to ENST00000503039 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr5:176477854 G>A maps to ENST00000503039 K232K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FD-A43X-01A-11D-A23U-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:53656991 G>A maps to NM_001172674.1 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr19:53644361 C>T maps to NM_001172674.1 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr19:53643915 G>C maps to NM_001172674.1 S723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z9-01A-11D-A26M-08 chr19:53644385 T>A maps to NM_001172674.1 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:53644298 C>T maps to NM_001172674.1 E595E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr19:53644379 T>C maps to NM_001172674.1 K568K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:53644385 T>A maps to NM_001172674.1 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr19:53644385 T>A maps to NM_001172674.1 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr19:53644385 T>A maps to NM_001172674.1 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr19:53644385 T>A maps to NM_001172674.1 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr19:52477606 G>A maps to NM_021632.3 Q3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr19:52468874 G>C maps to NM_021632.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr5:178140244 T>A maps to NM_005649.2 K212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr5:178152446 C>T maps to NM_005649.2 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr5:178140035 G>A maps to NM_005649.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YC-A9TC-01A-22D-A391-08 chr5:178140128 G>A maps to NM_005649.2 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr5:178139117 G>A maps to NM_005649.2 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:178310658 A>G maps to NM_058230.2 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr5:178310671 G>T maps to NM_058230.2 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr5:178310334 G>A maps to NM_058230.2 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr5:178506305 G>C maps to NM_014594.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr5:178506443 C>T maps to NM_014594.1 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:7585297 C>A maps to NM_018083.4 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:7584148 C>T maps to NM_018083.4 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr1:33745809 G>T maps to NM_152493.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr1:33764583 G>A maps to NM_152493.2 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr10:64159307 G>A maps to NM_014951.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr10:64415127 C>G maps to NM_199452.3 S43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr10:64136365 G>A maps to NM_199451.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr5:71740032 C>T maps to NM_152625.1 Q595Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr5:71756052 G>T maps to NM_152625.1 S424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr5:71756561 C>T maps to NM_152625.1 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr5:71756825 G>C maps to NM_152625.1 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr10:38407013 C>G maps to NM_003421.2 S312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr10:38407097 C>G maps to NM_003421.2 S340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr10:38407405 C>T maps to NM_003421.2 Q443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr10:38406652 C>T maps to NM_003421.2 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:37117314 C>T maps to NM_032825.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr19:37733937 C>G maps to NM_152604.1 S267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T3-01A-11D-A42E-08 chr19:37734206 C>T maps to NM_152604.1 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr19:37733678 C>T maps to NM_152604.1 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr19:37734532 C>T maps to NM_152604.1 L465L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ZF-A9RC-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:54765455 C>T maps to NM_001130967.1 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr2:180310453 T>C maps to NM_152520.4 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:180348113 G>C maps to NM_152520.4 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr2:180634383 G>A maps to NM_152520.4 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr2:180634320 G>A maps to NM_152520.4 N54N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:180308036 C>G maps to NM_152520.4 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr3:21552383 G>T maps to NM_024697.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:21466995 C>G maps to NM_024697.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:21462821 G>A maps to NM_024697.2 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr3:21478693 G>A maps to NM_024697.2 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:99097526 G>A maps to NM_032164.2 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr8:28207617 C>T maps to NM_018660.2 W430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr18:32954037 G>C maps to NM_145756.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr18:32844028 G>A maps to NM_001166012.1 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr7:148851341 G>A maps to NM_170686.2 Q110Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr19:44378164 C>T maps to ENST00000324394 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:72343145 G>T maps to NM_017757.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:72345582 A>C maps to NM_017757.2 R870R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr18:72775505 C>T maps to NM_017757.2 V1943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr18:72345799 C>G maps to NM_017757.2 S942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr18:72345041 C>A maps to NM_017757.2 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr18:72346208 C>G maps to NM_017757.2 L1078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr18:72343703 C>G maps to NM_017757.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr18:72344990 A>G maps to NM_017757.2 K672K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr18:72346256 C>T maps to NM_017757.2 I1094I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:46727043 C>G maps to NM_024741.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:47307917 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr23:47308244 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr23:47307190 C>T did not map to a codon.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr23:47307652 G>C did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr14:74360608 C>A maps to NM_021188.1 S48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr14:74370811 C>T maps to NM_021188.1 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr19:8576364 C>T maps to NM_032370.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:53612790 G>A maps to NM_001164309.1 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:58084191 T>C maps to NM_017879.1 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr19:58423470 G>C maps to NM_152475.2 Y40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:58437660 C>A maps to NM_133460.1 E630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:58438533 C>A maps to NM_133460.1 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FN-01A-11D-A31L-08 chr19:58438719 G>A maps to NM_133460.1 Q277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr19:58005152 G>T maps to NM_001098491.1 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr19:58005131 G>T maps to NM_001098491.1 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:37619282 C>T maps to NM_144689.3 Q464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA74-01A-11D-A391-08 chr19:37618252 C>T maps to NM_144689.3 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr19:37618201 G>A maps to NM_144689.3 Q103Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr16:49672369 G>A maps to NM_015069.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr16:49671946 G>A maps to NM_015069.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr16:49672360 G>A maps to NM_015069.2 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr16:49671466 G>C maps to NM_015069.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr16:49672417 G>A maps to NM_015069.2 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr16:49671862 G>A maps to NM_015069.2 D400D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr16:49670070 G>A maps to NM_015069.2 Q998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr16:49672246 G>A maps to NM_015069.2 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:148800825 G>A maps to NM_001001661.2 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:148801777 G>A maps to NM_001001661.2 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr7:148802518 G>C maps to NM_001001661.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr7:148801423 G>A maps to NM_001001661.2 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr7:148802179 G>A maps to NM_001001661.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr7:148802380 G>T maps to NM_001001661.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr7:148802641 G>A maps to NM_001001661.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr7:148809358 G>A maps to NM_001001661.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr7:148800825 G>A maps to NM_001001661.2 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:9639181 G>A maps to NM_024106.1 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr19:9639769 G>A maps to NM_024106.1 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr19:9639898 G>A maps to NM_024106.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:9640119 G>A maps to NM_024106.1 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:21719682 G>A maps to NM_001001415.2 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr19:21720335 C>G maps to NM_001001415.2 S494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:21720804 T>C maps to NM_001001415.2 H650H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RH-01A-11D-A30E-08 chr19:21713388 A>G did not map to a codon.
Sequencing variant TCGA-XF-A8HH-01A-11D-A38G-08 chr19:21720514 C>T maps to NM_001001415.2 Q554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:21990729 C>T maps to NM_003423.2 E703E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr19:21992382 C>G maps to NM_003423.2 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr19:21239809 T>C maps to NM_025189.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr19:21239682 C>G maps to NM_025189.3 S190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr19:21366259 C>G maps to NM_133473.2 S385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr19:52537104 C>T maps to NM_014650.2 K609K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr19:52538121 G>A maps to NM_014650.2 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:52538019 G>A maps to NM_014650.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TK-01A-42D-A339-08 chr19:52538019 G>A maps to NM_014650.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr19:52538327 C>A maps to NM_014650.2 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:12126041 G>T maps to NM_001080411.1 S547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN7-01A-11D-A42E-08 chr19:12126542 G>C maps to NM_001080411.1 S380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr1:23694480 G>A maps to NM_001077195.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R3-A69X-01A-22D-A30E-08 chr1:23694480 G>A maps to NM_001077195.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr1:23688593 G>A maps to NM_001077195.1 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr10:31137575 C>T maps to NM_182755.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr19:11976997 C>G maps to NM_152262.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:12383362 G>A maps to NM_001164276.1 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:11943308 C>T maps to NM_152357.2 Q440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr19:11943140 C>T maps to NM_152357.2 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:11942431 A>G maps to NM_152357.2 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr19:11942449 C>T maps to NM_152357.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr19:11943602 C>T maps to NM_152357.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr19:11890923 G>A maps to NM_152355.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R3-01A-11D-A38G-08 chr19:11892518 C>G maps to NM_152355.2 S627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr19:12462044 G>A maps to NM_030824.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr19:12461867 T>A maps to NM_030824.2 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr19:12541768 G>C maps to NM_005815.4 S406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr3:44490076 C>T maps to NM_181489.5 K362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:44497014 G>T maps to NM_181489.5 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr3:44488828 G>A maps to NM_181489.5 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr3:44496867 G>A maps to NM_181489.5 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr3:44496870 G>A maps to NM_181489.5 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:58989020 G>C maps to NM_017908.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr23:134494462 G>A did not map to a codon.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr23:134494182 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:44417604 G>C maps to NM_003425.3 V661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:44418217 G>C maps to NM_003425.3 S457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:44418822 C>T maps to NM_003425.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:44419121 T>A maps to NM_003425.3 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr6:57025900 C>T maps to NM_001031623.2 N1030N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr6:57012190 T>C maps to NM_001031623.2 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr6:57013306 C>T maps to NM_001031623.2 F808F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr5:178392388 T>C maps to NM_182594.2 Y328Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41Q-01A-11D-A339-08 chr5:178392139 A>G maps to NM_182594.2 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr19:57803579 A>G maps to NM_006635.3 E557E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:57802863 G>T maps to NM_006635.3 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr19:37130053 G>T maps to NM_153257.2 S398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr19:37129761 T>C maps to NM_153257.2 K495K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr19:37129878 G>C maps to NM_153257.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr9:109689831 G>A maps to NM_021224.4 Q1213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:109690176 C>G maps to NM_021224.4 L1328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMH-01A-11D-A42E-08 chr9:109691913 G>A maps to NM_021224.4 L1907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr19:53352430 G>A maps to NM_001008801.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr19:57085821 G>A maps to NM_001001668.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:57088107 C>A maps to NM_001001668.3 S104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr19:57085883 C>G maps to NM_001001668.3 S61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr19:57035985 A>T maps to NM_020813.2 K184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr19:57036529 G>A maps to NM_020813.2 W365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr19:50550280 C>T maps to NM_015428.1 Q861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:50542476 C>T maps to NM_015428.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr19:50542428 C>T maps to NM_015428.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr7:57188485 G>A maps to NM_033273.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr7:57188659 G>A maps to NM_033273.1 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:57193754 T>A maps to NM_033273.1 K78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:57188412 C>A maps to NM_033273.1 G237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr7:57188185 G>A maps to NM_033273.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr7:57188185 G>A maps to NM_033273.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr16:30410010 C>T maps to ENST00000495929 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr9:114296105 G>T maps to NM_133464.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr9:114296572 C>T maps to NM_133464.2 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr9:114304978 T>C maps to NM_133464.2 F588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr9:95609542 G>C maps to NM_031486.1 S509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr9:95618146 C>A maps to NM_031486.1 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr10:44112075 G>A maps to NM_145312.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr10:44112555 G>A maps to NM_145312.3 Q355Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr10:44112170 C>G maps to NM_145312.3 S227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr19:20308649 A>T maps to ENST00000428290 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr19:12691721 G>A maps to NM_020714.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:12691748 G>A maps to NM_020714.2 H380H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:11917626 C>T maps to NM_152356.3 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr19:22847803 G>T maps to NM_020855.2 G445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr19:22847049 A>G maps to NM_020855.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:21606209 C>G maps to NM_001076678.2 S250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr19:21606924 C>G maps to NM_001076678.2 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr19:21607133 C>A maps to NM_001076678.2 S558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:247464048 C>T maps to NM_032752.1 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:247464252 G>A maps to NM_032752.1 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R2-01A-11D-A391-08 chr1:247492646 C>T maps to NM_032752.1 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr1:247464420 G>A maps to NM_032752.1 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:58868470 G>A maps to NM_198458.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr19:58867573 C>G maps to NM_198458.1 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:58868554 G>A maps to NM_198458.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr7:99227061 G>T maps to NM_145115.2 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TE-01A-12D-A339-08 chr7:99227078 C>T maps to NM_145115.2 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr7:99227357 G>T maps to NM_145115.2 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr3:44776317 A>G maps to NM_145044.2 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr3:44776195 C>T maps to NM_145044.2 Q95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:44763164 C>T maps to NM_033210.4 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr3:44763892 C>T maps to NM_033210.4 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:77158842 C>T maps to NM_032772.4 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr19:19917757 G>A maps to NM_001099269.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr19:32845769 G>A maps to NM_014910.4 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:32845802 C>T maps to NM_014910.4 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:32844194 G>A maps to NM_014910.4 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr19:32843953 C>G maps to NM_014910.4 S73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr19:32843953 C>G maps to NM_014910.4 S73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr19:32843882 G>A maps to NM_014910.4 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6M-01A-11D-A391-08 chr9:99521602 G>A maps to NM_014930.1 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr9:99521167 C>T maps to NM_014930.1 R648R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr10:135123666 G>T did not map to a codon.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr2:27838102 C>T maps to NM_032434.2 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:27825412 C>G maps to NM_032434.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr2:27821011 G>A maps to NM_032434.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:27821095 G>A maps to NM_032434.2 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr20:62597636 G>A maps to NM_020713.1 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr20:62598083 T>C maps to NM_020713.1 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:27600418 G>T maps to NM_144631.4 S540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr2:27600945 G>A maps to NM_144631.4 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr2:27602984 G>A maps to NM_144631.4 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:95815562 G>A maps to NM_032788.1 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr2:95818968 G>A maps to NM_032788.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr2:95815295 C>A maps to NM_032788.1 G312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr18:74091603 G>A maps to ENST00000443185 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr18:74091003 G>A maps to ENST00000443185 G1022G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7PW-01A-11D-A34U-08 chr18:74074473 C>T maps to ENST00000443185 V1157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr18:74091294 G>A maps to ENST00000443185 F925F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr18:74091356 G>A maps to ENST00000443185 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78M-01A-21D-A34U-08 chr18:74083446 G>A maps to ENST00000443185 L1113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr18:74153894 C>A maps to ENST00000443185 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4T-01A-11D-A38G-08 chr18:74091846 C>A maps to ENST00000443185 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr8:146033635 C>T maps to NM_213605.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr8:146029039 C>T maps to NM_213605.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A61P-01A-11D-A30E-08 chr8:146029030 G>A maps to NM_213605.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr8:146033167 C>T maps to NM_213605.2 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr10:97916861 C>G maps to NM_014803.3 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr10:97916828 G>A maps to NM_014803.3 Q250Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:10446883 G>A maps to NM_053042.2 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr4:10444948 G>A maps to NM_053042.2 Q1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr18:14105971 T>C maps to NM_145287.3 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr18:22805189 C>A maps to NM_015461.2 E898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr18:22806432 G>A maps to NM_015461.2 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr18:22806744 C>T maps to NM_015461.2 K379K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr18:22671971 C>T maps to NM_015461.2 L1244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN2-01A-11D-A42E-08 chr18:22805859 G>A maps to NM_015461.2 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr18:22671935 G>A maps to NM_015461.2 F1256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr18:22806822 G>A maps to NM_015461.2 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr19:56113615 C>G maps to NM_153219.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA51-01A-21D-A391-08 chr19:56113489 C>G maps to NM_153219.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:42729169 C>G maps to NM_133444.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:42730255 C>G maps to NM_133444.1 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:42728830 G>A maps to NM_133444.1 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SP-01A-11D-A391-08 chr19:37879586 C>G maps to NM_032453.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr19:37879872 G>T maps to NM_032453.1 G308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:52919779 C>T maps to NM_032423.2 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr19:52909829 C>T maps to NM_032423.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr19:37045698 C>A did not map to a codon.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr19:37037818 C>T maps to NM_001145649.1 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:58117276 G>A maps to NM_020880.3 W128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr18:56585881 G>A maps to NM_018181.4 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr18:56586340 C>T maps to NM_018181.4 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4U-01A-11D-A38G-08 chr18:56586091 G>A maps to NM_018181.4 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:52937205 A>G did not map to a codon.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:52942470 C>A maps to NM_001143939.1 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr19:31039639 A>G maps to NM_014717.1 T1038T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LA-01A-11D-A18F-08 chr19:30935446 C>T maps to NM_014717.1 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:31040308 G>A maps to NM_014717.1 P1261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr19:30935716 C>T maps to NM_014717.1 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:31039180 G>A maps to NM_014717.1 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B0-01A-11D-A31L-08 chr19:30936562 C>T maps to NM_014717.1 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr19:31040176 C>T maps to NM_014717.1 P1217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TH-01A-11D-A32B-08 chr19:31039429 C>T maps to NM_014717.1 S968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr19:31040188 G>T maps to NM_014717.1 L1221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr19:31039135 G>A maps to NM_014717.1 S870S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:30934885 C>T maps to NM_014717.1 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A5RJ-01A-11D-A289-08 chr19:31039238 C>T maps to NM_014717.1 Q905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr19:31039207 C>T maps to NM_014717.1 S894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr19:31038923 C>T maps to NM_014717.1 R800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr19:30935047 C>T maps to NM_014717.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr19:30936328 G>A maps to NM_014717.1 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr19:38102906 C>T maps to NM_152606.3 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:38102910 G>T maps to NM_152606.3 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:38090567 G>A maps to NM_152606.3 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr19:57832231 C>A maps to NM_213598.3 S4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr19:58773726 C>T maps to NM_014480.2 F585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr19:40519755 T>C maps to NM_178544.3 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr19:57888494 G>A did not map to a codon.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr19:57888565 C>A maps to NM_173631.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:57889441 C>T maps to NM_173631.2 H366H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:57910374 C>T maps to NM_001172773.1 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:57910012 C>T maps to NM_001172773.1 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:57908460 G>T maps to NM_001172773.1 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:58049010 C>T maps to ENST00000376233 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:58198131 G>A maps to ENST00000356715 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr19:58196671 G>T maps to ENST00000356715 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:58198068 C>T maps to ENST00000356715 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr19:58199364 C>G maps to ENST00000356715 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr19:58199364 C>G maps to ENST00000356715 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47Y-01A-11D-A23U-08 chr19:58320106 C>A maps to NM_024762.3 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr19:58324668 G>A maps to NM_024762.3 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr19:2834825 G>A maps to NM_001102651.1 Q531Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr19:2852821 G>A maps to NM_152791.4 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:2852509 A>G maps to NM_152791.4 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:2853250 T>A maps to NM_152791.4 Y396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:2851464 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:2876262 G>A maps to NM_024967.1 E101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr19:2877543 T>G maps to NM_024967.1 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr19:2877834 G>A maps to NM_024967.1 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:7083112 C>T maps to NM_024341.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:7083275 G>T maps to NM_024341.2 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:7083364 C>T maps to NM_024341.2 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr19:8922083 G>C maps to NM_144693.1 S361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr19:8932722 G>A maps to NM_144693.1 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr19:9453062 C>G maps to NM_032497.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr19:9577280 G>C maps to NM_152476.2 S781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr19:9577963 G>A maps to NM_152476.2 F553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:9583924 G>C maps to NM_152476.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr19:9581977 T>A maps to NM_152476.2 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr19:9577798 G>C maps to NM_152476.2 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:9721763 G>A maps to NM_152289.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:9764311 G>A maps to NM_001130032.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr19:12430205 T>C maps to NM_145276.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:12639429 G>C maps to NM_144976.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:36673471 G>A maps to ENST00000355114 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:36940184 G>T maps to NM_001145343.1 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA82-01A-11D-A391-08 chr19:37211101 C>T maps to ENST00000423498 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:37211047 G>A maps to ENST00000423498 E473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:37209898 A>G maps to ENST00000423498 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:37210523 C>T maps to ENST00000423498 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr19:37210585 C>T maps to ENST00000423498 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:37441803 G>A maps to NM_198539.2 E583E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:37441473 T>G maps to NM_198539.2 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:37441533 G>A maps to NM_198539.2 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr19:37916820 C>A maps to NM_152484.2 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:37903714 G>A maps to NM_152484.2 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:37916854 G>A maps to NM_152484.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr19:37903794 G>A maps to NM_152484.2 Q589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr19:37904634 G>A maps to NM_152484.2 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr19:37966851 C>T maps to NM_144694.1 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:37975904 C>T maps to NM_144694.1 Q461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr19:38055592 G>A maps to NM_016536.3 I579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr19:38055988 A>G maps to NM_016536.3 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr19:38055682 C>G maps to NM_016536.3 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr8:125989772 C>T maps to NM_152412.2 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr8:125987910 C>G maps to NM_152412.2 S10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr8:125990083 C>G maps to NM_152412.2 S525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr19:38229522 G>C maps to NM_001172690.1 S623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr19:38262255 C>T maps to NM_001172690.1 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:38231069 G>A maps to NM_001172690.1 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:38229485 C>T maps to NM_001172690.1 E635E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr19:42583493 G>T maps to ENST00000222339 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:42583876 C>T maps to ENST00000222339 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr19:42583135 C>G maps to ENST00000222339 Y216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr19:42582871 C>T maps to ENST00000222339 H128H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:52375789 C>A maps to NM_032679.2 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:52381646 G>C maps to NM_032679.2 S61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:53014287 C>G maps to NM_001099694.1 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr19:53014784 C>G maps to NM_001099694.1 S384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:56156282 G>T maps to NM_016535.3 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:56895394 G>C maps to NM_144690.1 S464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr19:56934755 T>G maps to NM_001159861.1 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:56934717 C>T maps to NM_001159861.1 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:56935484 T>C maps to NM_001159861.1 H486H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr19:37642531 G>A maps to ENST00000356958 Q757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:37647135 G>C maps to ENST00000356958 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr19:37643203 G>A maps to ENST00000356958 Q533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA89-01A-11D-A391-08 chr19:37678027 C>T maps to NM_152279.3 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:37678105 G>A maps to NM_152279.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:58291115 G>A maps to NM_017652.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:58371384 C>T maps to NM_032828.2 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr19:58361438 G>A maps to NM_032828.2 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:58370964 C>T maps to NM_032828.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:58371261 C>T maps to NM_032828.2 C494C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A6ZA-01A-12D-A339-08 chr19:58370722 C>T maps to NM_032828.2 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr19:58367497 G>T maps to NM_032828.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr3:48310140 C>T maps to NM_016089.2 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr15:85341885 C>G maps to NM_014630.2 S935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr17:5086348 C>T maps to NM_032530.1 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:5087089 T>G maps to NM_032530.1 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr17:5086480 G>A maps to NM_032530.1 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr8:195299 G>A maps to NM_001042416.1 W151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr16:3493129 G>A maps to NM_152457.1 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr16:3490852 G>A maps to NM_152457.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr16:2052219 C>T maps to ENST00000431526 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:35250829 G>A maps to NM_001007248.2 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr19:53269907 G>A maps to NM_198457.2 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr19:53270155 G>A maps to NM_198457.2 Q285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr19:53270960 G>A maps to NM_198457.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr19:58500014 C>T maps to NM_025027.3 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr19:58491153 G>A maps to NM_025027.3 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr19:58511211 C>T maps to NM_025027.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:38200663 G>A maps to NM_032689.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A5W6-01A-11D-A289-08 chr5:123979265 C>A maps to NM_020747.2 E1412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:124036908 G>A maps to NM_020747.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:124080027 G>A maps to NM_020747.2 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:124036728 G>A maps to NM_020747.2 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BY-01A-31D-A289-08 chr5:124036908 G>A maps to NM_020747.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr5:123983601 T>C maps to NM_020747.2 K825K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr5:123982615 G>C maps to NM_020747.2 S1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr5:124036743 C>A maps to NM_020747.2 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr15:64970529 C>T maps to NM_015042.1 P1206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr15:64968121 G>A maps to NM_015042.1 K1023K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr15:64970406 C>T maps to NM_015042.1 R1165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA58-01A-12D-A42E-08 chr19:52852448 G>A maps to NM_001161425.1 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr19:53209075 G>C maps to NM_001161500.1 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr19:53209408 G>T maps to NM_001161500.1 S300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3L-01A-11D-A38G-08 chr19:53208599 C>A maps to NM_001161500.1 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr19:52448419 T>C maps to NM_001031721.3 Y428Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TG-01A-11D-A32B-08 chr19:52448026 C>T maps to NM_001031721.3 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:52443460 G>A did not map to a codon.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr19:52519707 G>A maps to NM_025040.3 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:52519934 G>A maps to NM_025040.3 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:52498045 G>A maps to ENST00000354939 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:52498090 C>A did not map to a codon.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr19:52497323 C>T maps to ENST00000354939 Q346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr19:52497182 G>C maps to ENST00000354939 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr19:52498045 G>A maps to ENST00000354939 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A6MB-01A-11D-A31L-08 chr19:52496423 C>T maps to ENST00000354939 K646K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMY-01A-11D-A42E-08 chr19:52497332 A>C maps to ENST00000354939 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr19:52619319 G>C maps to NM_178523.3 S366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:52618745 G>A maps to NM_178523.3 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:52618286 G>A maps to NM_178523.3 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:52619162 G>A maps to NM_178523.3 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41S-01A-12D-A339-08 chr19:52618826 G>A maps to NM_178523.3 F530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr9:116812344 G>A maps to ENST00000374126 G921G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:40529227 C>T maps to NM_001145082.2 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TD-01A-51D-A339-08 chr3:40528372 G>A maps to NM_001145082.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr3:40553061 G>A maps to NM_175888.2 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr5:16465636 G>T maps to NM_033414.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:16453157 G>A maps to NM_033414.2 Q424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:144733611 G>T maps to NM_014789.3 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr8:144732815 G>T maps to NM_014789.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr8:144732158 G>A maps to NM_014789.3 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr17:16526921 C>T maps to NM_020787.3 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr17:16527692 C>T maps to NM_020787.3 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr19:20807107 T>C maps to NM_001076675.2 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:20807985 C>A maps to NM_001076675.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42Q-01A-11D-A23U-08 chr19:20808061 G>C maps to NM_001076675.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr19:55993618 G>T maps to NM_033113.2 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:55992895 C>T maps to NM_033113.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr19:55994179 C>T maps to NM_033113.2 C536C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr19:55995160 C>T maps to NM_033113.2 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr16:30794835 G>A maps to NM_001080417.1 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:30795475 G>C maps to NM_001080417.1 S58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:30793986 G>A maps to NM_001080417.1 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:30794556 G>A maps to NM_001080417.1 H364H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr23:47918816 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA6Q-01A-11D-A391-08 chr23:47920264 C>G did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:47919865 C>T did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr23:47919397 C>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr23:47918066 T>C did not map to a codon.
Sequencing variant TCGA-2F-A9KT-01A-11D-A38G-08 chr2:71577397 G>A maps to NM_014497.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr2:71597021 G>T maps to NM_014497.3 E718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr2:71650276 G>A maps to NM_014497.3 K1211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr2:71660292 A>G did not map to a codon.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:71658554 G>T maps to NM_014497.3 E1917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr3:179051360 C>G maps to NM_016331.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr12:48736908 C>T maps to NM_152320.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:48739258 T>A did not map to a codon.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr1:40960596 G>A maps to NM_198494.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr1:40923059 G>T maps to NM_023070.2 G129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr1:40928687 C>T maps to NM_023070.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:91405314 G>A maps to NM_201269.1 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr23:22291956 G>A did not map to a codon.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr23:22291895 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr23:22291513 C>T did not map to a codon.
Sequencing variant TCGA-K4-A6FZ-01A-11D-A31L-08 chr23:22291225 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:31088002 G>T maps to NM_014699.3 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:31090755 C>T maps to NM_014699.3 C1037C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr16:31087978 G>T maps to NM_014699.3 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr16:31090893 C>T maps to NM_014699.3 V1083V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr16:31089288 G>T maps to NM_014699.3 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:31092966 C>T maps to NM_014699.3 I1774I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:182025729 G>A maps to NM_001009992.1 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr1:182026764 G>A maps to NM_001009992.1 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X2-01A-11D-A22Z-08 chr19:52394761 G>A maps to NM_023074.3 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr19:52393871 C>T maps to NM_023074.3 *506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr17:47395036 C>T maps to NM_014897.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:47394736 G>A maps to NM_014897.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:11609126 C>T maps to NM_138783.3 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr19:11598431 A>T maps to NM_138783.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr19:11594541 G>A maps to NM_138783.3 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41P-01A-12D-A339-08 chr3:88188969 G>A maps to NM_018293.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:99170384 G>A maps to NM_001083956.1 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:99170441 G>A maps to NM_001083956.1 E272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr9:40773178 G>C maps to NM_033160.5 S699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr9:40772769 G>A maps to NM_033160.5 F835F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr3:44636002 T>G maps to NM_173658.1 Y106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RL-01A-11D-A38G-08 chr3:44636136 C>G maps to NM_173658.1 S151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr3:42956609 C>T maps to NM_001134656.1 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr12:124497234 C>T maps to NM_152437.1 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr19:53678788 G>A maps to NM_024733.3 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:53668817 G>A maps to NM_024733.3 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr19:53667756 G>C maps to NM_024733.3 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr19:53668481 G>A maps to NM_024733.3 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr19:53669302 G>T maps to NM_024733.3 S147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr19:53668145 G>A maps to NM_024733.3 Q533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:56969550 C>A maps to ENST00000342634 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr19:56953097 C>T maps to ENST00000342634 K550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr19:56972124 C>G maps to ENST00000342634 L124L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-A6B2-01A-11D-A30E-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:31075324 G>A maps to NM_001172669.1 L175L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-SY-A9G5-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-SY-A9G5-01A-11D-A38G-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr1:247202110 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:247200918 C>A maps to NM_033213.3 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA81-01A-11D-A391-08 chr19:58238812 G>A maps to ENST00000335820 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr19:58238779 C>T maps to ENST00000335820 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:58232820 C>T maps to ENST00000335820 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43N-01A-11D-A23U-08 chr19:58238842 G>T maps to ENST00000335820 C18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr19:58232718 T>C maps to ENST00000335820 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr19:58232607 C>T maps to ENST00000335820 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-AAQO-01A-11D-A38G-08 chr19:58238779 C>T maps to ENST00000335820 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr1:249142537 C>T maps to NM_024836.1 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr23:46322679 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr23:46332192 C>A did not map to a codon.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr23:46359821 G>C did not map to a codon.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr23:46359667 C>G did not map to a codon.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr23:46359692 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:23845929 C>A maps to NM_138330.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr19:23837400 G>A maps to NM_138330.2 Q112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:23836172 G>C maps to NM_138330.2 S521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KP-01A-11D-A38G-08 chr19:22364164 A>G maps to NM_001001411.2 Y118Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr19:22375855 C>T maps to NM_001001411.2 W31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr19:22375889 G>A maps to NM_001001411.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr19:53740296 A>G maps to NM_182609.2 H561H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SX-01A-21D-A391-08 chr1:227842169 G>A maps to NM_178549.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:63726502 C>A maps to NM_153363.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:23938260 C>G maps to NM_138286.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr19:23927313 G>A maps to NM_138286.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:23926434 A>G maps to NM_138286.2 N639N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:20117296 C>T maps to NM_033196.2 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr19:20118010 C>A maps to NM_033196.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:151261979 C>G maps to NM_020832.1 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:151259813 C>T maps to NM_020832.1 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:151261859 C>T maps to NM_020832.1 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr1:151260359 C>T maps to NM_020832.1 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr1:151260648 C>T maps to NM_020832.1 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr1:151259024 C>G maps to NM_020832.1 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:30581605 G>C maps to NM_145271.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:30581749 G>T maps to NM_145271.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr16:30583533 G>A maps to NM_001024683.1 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr16:30583542 C>A maps to NM_001024683.1 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62O-01A-11D-A30E-08 chr16:30616193 G>A maps to NM_138447.1 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr16:30616004 G>C maps to NM_138447.1 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr16:30620933 G>A maps to NM_138447.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:12014494 C>T maps to ENST00000429654 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr1:43317429 C>T maps to ENST00000442768 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr1:249144980 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr1:249144437 G>A maps to NM_001136036.2 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr1:247151489 C>T maps to NM_020394.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr8:144377991 C>A maps to NM_030895.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr8:144378882 G>A maps to NM_030895.2 E346E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr8:144378378 G>A maps to NM_030895.2 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr19:9407521 G>C maps to NM_198535.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr19:9408080 G>A maps to NM_198535.1 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SK-01A-11D-A42E-08 chr19:9407299 G>A maps to NM_198535.1 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97P-01A-11D-A38G-08 chr8:146067712 C>T maps to ENST00000446747 H417H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr8:146068515 C>G maps to ENST00000446747 S685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr8:146068075 C>G maps to ENST00000446747 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr8:146067296 C>T maps to ENST00000446747 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:24086953 G>C maps to NM_021916.2 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr22:24086127 G>A maps to NM_021916.2 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B2-01A-11D-A30E-08 chr22:24086358 G>A maps to NM_021916.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N6-01A-11D-A21A-08 chr22:24086628 G>A maps to NM_021916.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78L-01A-12D-A339-08 chr22:24087104 G>A maps to NM_021916.2 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:12060203 C>T maps to NM_144566.1 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr19:12059540 C>T maps to NM_144566.1 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:12059828 G>C maps to NM_144566.1 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:12060203 C>T maps to NM_144566.1 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr8:37554676 G>A maps to NM_025069.1 K86K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R4-01A-11D-A38G-08 chr8:37554778 G>A maps to NM_025069.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PF-01A-11D-A38G-08 chr8:81599685 G>A maps to NM_001033723.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A762-01A-11D-A339-08 chr8:144776540 C>T maps to NM_173831.3 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6W-01A-12D-A391-08 chr19:21477263 G>A maps to NM_021269.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA5H-01A-11D-A391-08 chr19:12575379 C>T maps to ENST00000428311 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr19:57133965 G>A maps to NM_021216.4 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:57132855 C>G maps to NM_021216.4 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A6MD-01A-41D-A34U-08 chr19:57133341 C>T maps to NM_021216.4 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr19:57133449 C>G maps to NM_021216.4 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr15:90622958 C>T maps to NM_198526.2 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr15:90617418 C>T maps to NM_198526.2 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr15:90622890 G>C did not map to a codon.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr23:84523328 G>T did not map to a codon.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr23:84510443 G>T did not map to a codon.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr23:84510755 G>A did not map to a codon.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr23:84519435 G>C did not map to a codon.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr23:84510741 T>C did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr23:84510341 G>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:56007095 C>A maps to NM_182633.1 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr19:21281117 G>A did not map to a codon.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr19:21300900 G>A maps to NM_182515.3 E477E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr19:21300015 G>A maps to NM_182515.3 K182K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr7:57528874 T>C maps to NM_001159279.1 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PE-01A-11D-A38G-08 chr7:57529051 C>A maps to NM_001159279.1 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4N-01A-11D-A38G-08 chr7:57529008 C>G maps to NM_001159279.1 S281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:435804 C>T maps to NM_133474.2 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr4:437484 G>A maps to NM_133474.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr4:435693 T>C maps to NM_133474.2 V854V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:265127 C>T maps to ENST00000419098 E506E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:266003 C>T maps to ENST00000419098 E214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr19:20728096 C>T maps to NM_001159293.1 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr19:20727611 G>C maps to NM_001159293.1 S466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr19:20728549 G>C maps to NM_001159293.1 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr22:20760363 C>T maps to NM_003426.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr22:20760951 C>T maps to NM_003426.2 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr22:20760783 C>G maps to NM_003426.2 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr22:20759740 G>T maps to NM_003426.2 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr12:53579199 G>A maps to NM_001004304.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr7:149172353 C>T maps to NM_001163474.1 E353E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr16:30545883 G>A maps to NM_023931.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr19:57955391 C>T maps to NM_001023561.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:57956148 C>T maps to NM_001023561.2 Q545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:80789061 C>T maps to NM_024702.2 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr17:80788478 G>A maps to NM_024702.2 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr17:80788248 C>T maps to NM_024702.2 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr17:80789144 C>A maps to NM_024702.2 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr17:80788040 G>A maps to NM_024702.2 R717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr23:134427832 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr23:134427902 A>T did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr23:134421721 C>T did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:134428062 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr23:134425015 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr23:134427716 A>G did not map to a codon.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr23:134425472 C>G did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:134421477 C>G did not map to a codon.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr23:134427984 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:134424952 C>G did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:134427802 G>A did not map to a codon.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr23:134425451 C>G did not map to a codon.
Sequencing variant TCGA-ZF-AA52-01A-12D-A391-08 chr23:134424952 C>G did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr6:35260388 G>A maps to NM_003427.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr6:35259395 C>T maps to NM_003427.3 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr19:53958819 T>C maps to NM_001008401.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr19:53958024 G>A maps to NM_001008401.3 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr19:53958359 C>A maps to NM_001008401.3 S200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr19:53912232 C>T maps to NM_001040185.1 F475F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SV-01A-21D-A42E-08 chr19:53911281 G>A maps to NM_001040185.1 E158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:52785368 C>T maps to NM_001010851.2 H8H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:52793452 C>T maps to NM_001010851.2 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A54R-01A-11D-A26M-08 chr19:52793745 G>A maps to NM_001010851.2 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr16:30536209 G>A maps to NM_024671.3 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:30536398 G>A maps to NM_024671.3 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr16:30536746 G>C maps to NM_024671.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr16:30537306 C>A maps to NM_024671.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:2933591 C>G maps to NM_021217.2 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LC-A66R-01A-41D-A30E-08 chr19:2933518 G>A maps to NM_021217.2 Q536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PQ-A6FI-01A-11D-A31L-08 chr19:2934746 A>C maps to NM_021217.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr19:2939324 G>C maps to NM_021217.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:35275415 G>A maps to NM_014106.3 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:58011447 G>A maps to ENST00000332030 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA76-01A-11D-A391-08 chr15:90903560 C>T maps to NM_001004309.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr15:90903738 C>T maps to NM_001004309.2 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DU-01A-11D-A32B-08 chr7:150094000 C>T maps to NM_173680.3 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr19:58265745 G>A maps to NM_173632.3 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T5-01A-11D-A42E-08 chr19:58262208 C>G maps to NM_173632.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr7:149152302 G>T maps to ENST00000440594 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr7:149129349 C>T maps to ENST00000440594 K672K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr16:89288575 G>A maps to NM_182531.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:40580723 G>C maps to NM_001142577.1 S543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KR-01A-11D-A38G-08 chr19:40540725 A>G maps to NM_001005851.2 R680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:40541189 C>A maps to NM_001005851.2 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:40542232 G>C maps to NM_001005851.2 S178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6R-01A-11D-A42E-08 chr19:40541541 C>T maps to NM_001005851.2 Q408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr19:40540935 C>T maps to NM_001005851.2 E610E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47T-01A-11D-A23U-08 chr19:38161001 A>G maps to NM_152605.3 C16C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:38160215 G>A maps to NM_152605.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA84-01A-11D-A391-08 chr9:99581011 G>A maps to NM_001001662.1 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr16:30594498 G>A maps to NM_152458.6 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr16:30594231 G>A maps to NM_152458.6 C289C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr16:30596746 G>A maps to NM_152458.6 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr16:30594114 G>C maps to NM_152458.6 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr7:148768419 G>A maps to NM_152411.3 Q482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr7:148769088 G>A maps to NM_152411.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42E-01A-11D-A23U-08 chr7:148768285 C>T maps to NM_152411.3 E526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:148769074 C>T maps to NM_152411.3 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4U1-01A-11D-A31L-08 chr7:148767619 C>A maps to NM_152411.3 A748A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr7:148769266 G>A maps to NM_152411.3 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr7:148768419 G>A maps to NM_152411.3 Q482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr7:148768942 T>C maps to NM_152411.3 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr7:99084232 G>T maps to NM_213603.2 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78N-01A-12D-A339-08 chr9:130206794 C>T maps to NM_007135.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr19:12739531 C>T maps to NM_153358.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr19:12738663 A>G maps to NM_153358.2 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:12739579 G>T maps to NM_153358.2 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:12739036 C>T maps to NM_153358.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:12735495 C>T maps to NM_153358.2 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A6I1-01A-12D-A31L-08 chr19:12740068 C>T maps to NM_153358.2 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:35449695 G>A maps to NM_175872.4 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr19:35449113 G>A maps to NM_175872.4 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41O-01A-12D-A34U-08 chr19:35448985 C>T maps to NM_175872.4 E591E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SJ-01A-11D-A391-08 chr19:35450034 C>A maps to NM_175872.4 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:38028267 C>T maps to NM_001013659.2 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMW-01A-11D-A42E-08 chr19:58806613 T>C maps to NM_021089.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PD-01A-11D-A38G-08 chr3:113955561 G>C maps to NM_007136.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr7:127014079 G>C maps to NM_176814.3 S437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr7:127014672 G>A maps to NM_176814.3 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A7I0-01A-22D-A34U-08 chr2:185802576 A>G maps to NM_194250.1 R818R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B4-01A-12D-A202-08 chr2:185800684 G>T maps to NM_194250.1 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:185803227 G>A maps to NM_194250.1 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr2:185803728 C>T maps to NM_194250.1 V1202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr2:185798460 G>T did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr2:185803314 G>A maps to NM_194250.1 K1064K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr2:185731217 A>T maps to NM_194250.1 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr2:185798353 G>T maps to NM_194250.1 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr2:185800632 G>A maps to NM_194250.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMX-01A-11D-A42E-08 chr2:185802306 A>G maps to NM_194250.1 K728K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr2:185802324 G>A maps to NM_194250.1 Q734Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62S-01A-11D-A30E-08 chr7:88964632 A>G maps to NM_181646.2 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr7:88963714 T>C maps to NM_181646.2 Y473Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr7:88847590 T>G maps to NM_181646.2 Y77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr7:88966096 C>G maps to NM_181646.2 P1267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr7:88963951 T>C maps to NM_181646.2 Y552Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr19:53057324 C>T maps to NM_001039886.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr19:53056703 C>T maps to NM_001039886.3 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr19:53056855 A>G maps to NM_001039886.3 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr19:53057056 C>T maps to NM_001039886.3 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:47774799 G>T did not map to a codon.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr23:47775380 C>G did not map to a codon.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr23:47776022 C>T did not map to a codon.
Sequencing variant TCGA-ZF-A9R7-01A-11D-A38G-08 chr23:47774576 C>T did not map to a codon.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr19:53994368 G>T maps to NM_001004301.3 G295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr19:53994028 T>G maps to NM_001004301.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr19:58384993 G>A maps to NM_001144989.1 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr19:53453509 C>T maps to NM_001031665.1 E506E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:53454541 C>T maps to NM_001031665.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr19:53454400 C>T maps to NM_001031665.1 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4V-01A-11D-A38G-08 chr19:53454142 A>G maps to NM_001031665.1 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr19:11834015 C>A maps to NM_001080493.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:146823423 C>T maps to ENST00000508784 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr4:146824008 G>A maps to ENST00000508784 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr4:146824286 C>A maps to ENST00000508784 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr13:115090579 A>G maps to NM_032436.2 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA80-01A-11D-A391-08 chr19:37382848 G>A maps to NM_001171979.1 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr19:37383320 G>A maps to NM_001171979.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:37382766 G>C maps to NM_001171979.1 S390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMJ-01A-11D-A42E-08 chr19:37383158 A>G maps to NM_001171979.1 H259H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7M-01A-11D-A391-08 chr17:33288932 G>A maps to NM_052857.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:33288629 G>A maps to NM_052857.3 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:33288629 G>C maps to NM_052857.3 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr20:57767954 G>T maps to NM_178457.1 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr20:57767396 C>T maps to NM_178457.1 D441D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr20:57768851 T>A maps to NM_178457.1 P926P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr20:57769598 C>G maps to NM_178457.1 P1175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5C0-01A-11D-A289-08 chr20:57766760 G>A maps to NM_178457.1 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr20:57829686 C>T maps to NM_178457.1 A1641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr20:57768401 C>T maps to NM_178457.1 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3C-01A-21D-A391-08 chr20:57828951 G>T did not map to a codon.
Sequencing variant TCGA-XF-AAN3-01A-11D-A42E-08 chr20:57767297 C>T maps to NM_178457.1 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RD-01A-11D-A42E-08 chr20:57767093 G>A maps to NM_178457.1 E340E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4W-01A-12D-A38G-08 chr20:57768113 C>G maps to NM_178457.1 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA86-01A-11D-A391-08 chr19:52659998 G>A maps to NM_001102657.1 Q313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:52663829 G>A maps to NM_001102657.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr19:52659357 G>A maps to NM_001102657.1 Y526Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr19:52658815 G>C maps to NM_001102657.1 S707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr19:52658462 G>A maps to NM_001102657.1 Q825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr19:52659498 G>A maps to NM_001102657.1 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:52663799 C>T maps to NM_001102657.1 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:52659765 T>G maps to NM_001102657.1 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr14:102808515 G>C maps to NM_018335.3 *928Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2F-A9KO-01A-11D-A38G-08 chr19:52569144 G>A maps to NM_001136499.1 Q664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:52568425 G>A maps to NM_001136499.1 N903N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr19:52570183 G>C maps to NM_001136499.1 Y317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:12187084 G>T maps to NM_001136501.1 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A4TZ-01A-11D-A31L-08 chr19:12187239 C>T maps to NM_001136501.1 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TA-01A-12D-A339-08 chr19:12187309 C>T maps to NM_001136501.1 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:53854451 C>G maps to NM_138374.1 S175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr19:53848761 C>T maps to NM_138374.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SY-01A-21D-A42E-08 chr19:53856111 C>T maps to NM_138374.1 F728F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr19:53855283 G>A maps to NM_138374.1 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:9873967 G>A maps to NM_001077624.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:9868233 C>A maps to NM_001077624.1 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:9868196 G>C maps to NM_001077624.1 S519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr19:9869188 C>T maps to NM_001077624.1 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:21132775 G>T maps to NM_003429.4 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:21131622 G>C maps to NM_003429.4 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr19:21131733 C>T maps to NM_003429.4 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A47X-01A-31D-A23U-08 chr3:32031023 C>T maps to NM_001137674.1 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr3:32032112 A>G maps to NM_001137674.1 E514E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr7:149557964 G>A maps to NM_001099220.1 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SZ-01A-11D-A391-08 chr7:149558882 A>T maps to NM_001099220.1 A878A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:12154850 T>C maps to NM_001080404.1 Q502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr19:12156002 G>T maps to NM_001080404.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:12154730 G>A maps to NM_001080404.1 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:12155621 G>A maps to NM_001080404.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:12156002 G>C maps to NM_001080404.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr19:12154835 G>A maps to NM_001080404.1 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr19:52887594 C>G maps to NM_001145434.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr19:20215089 G>T maps to NM_007138.1 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr19:23545342 G>T maps to NM_003430.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr19:23556628 G>C maps to NM_003430.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SM-01A-11D-A42E-08 chr19:23542760 G>C maps to NM_003430.2 S1007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr7:64863320 G>C maps to NM_152626.2 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:64863788 G>A maps to NM_152626.2 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RG-01A-21D-A42E-08 chr7:64864591 C>G maps to NM_152626.2 S522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr19:20044216 G>T maps to NM_031218.3 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YF-AA3M-01A-11D-A42E-08 chr19:20027396 C>T maps to NM_031218.3 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6P-01A-11D-A391-08 chr19:22574716 G>C maps to NM_001098626.1 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr19:22586236 A>G maps to NM_001098626.1 N36N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A541-01A-11D-A26M-08 chr19:22941018 T>G maps to ENST00000397104 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:22940550 A>C maps to ENST00000397104 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:22939879 A>T maps to ENST00000397104 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATP-01A-11D-A391-08 chr19:22939105 A>G maps to ENST00000397104 T1005T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN0-01A-11D-A42E-08 chr19:22940641 G>C maps to ENST00000397104 S599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAN5-01A-11D-A42E-08 chr19:22940046 T>G maps to ENST00000397104 R762R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A72E-01A-12D-A339-08 chr20:47888078 G>A maps to NM_021035.2 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr20:47888255 A>G maps to NM_021035.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:47865809 G>A maps to NM_021035.2 R1251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr20:47886965 G>A maps to NM_021035.2 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr20:47886896 G>A maps to NM_021035.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SY-A9G5-01A-11D-A38G-08 chr20:47864403 C>T maps to NM_021035.2 L1719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr20:47888219 G>A maps to NM_021035.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr20:47870307 C>T maps to NM_021035.2 P1000P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr11:64884236 C>A maps to NM_014205.2 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr11:64884162 C>G maps to NM_014205.2 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr17:34851109 C>T maps to NM_004773.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:86123572 C>T maps to NM_017953.3 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr7:30395342 G>A did not map to a codon.
Sequencing variant TCGA-4Z-AA7Q-01A-11D-A391-08 chr22:29442813 C>T maps to NM_032173.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SG-01A-12D-A42E-08 chr19:5456731 G>C maps to NM_181710.3 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr11:60635045 C>G maps to NM_207341.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:60636672 C>T maps to NM_207341.2 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAML-01A-11D-A42E-08 chr11:60640680 C>T maps to NM_207341.2 Q387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:21214521 C>T maps to NM_003460.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WY-01A-11D-A22Z-08 chr16:21210984 G>A maps to NM_003460.1 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr16:21211120 C>T maps to NM_003460.1 Q591Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PH-01A-11D-A38G-08 chr16:21209160 G>T maps to NM_003460.1 S674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMT-01A-11D-A42E-08 chr16:21213483 G>A maps to NM_003460.1 Q410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr7:76062300 G>A maps to NM_001110354.1 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:238048518 G>A maps to NM_021186.3 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr1:238050137 C>A maps to NM_021186.3 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:238053788 T>C maps to NM_021186.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:238049173 G>A maps to NM_021186.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:238049176 G>C maps to NM_021186.3 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A83P-01A-11D-A34U-08 chr1:238053227 G>T maps to NM_021186.3 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41N-01A-11D-A339-08 chr1:238050712 C>A maps to NM_021186.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr1:238053884 C>G maps to NM_021186.3 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RN-01A-11D-A42E-08 chr7:50121394 A>G maps to NM_007009.2 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:38027017 G>T maps to NM_199321.2 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43P-01A-31D-A23U-08 chr17:38028661 C>T maps to NM_199321.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMG-01A-11D-A42E-08 chr17:38027759 G>T maps to NM_199321.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A5KE-01A-11D-A289-08 chr3:102176675 T>G maps to NM_175056.1 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7DV-01A-11D-A339-08 chr3:102187945 C>G maps to NM_175056.1 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:126631752 C>T maps to NM_017580.2 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr2:136111038 G>A maps to NM_032143.2 Q114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:136107718 C>T maps to NM_032143.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr2:136111057 T>A maps to NM_032143.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5N-A9KI-01A-31D-A42E-08 chr23:15821823 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:15809080 G>A did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:15821883 G>A did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr23:15818000 C>G did not map to a codon.
Sequencing variant TCGA-HQ-A5NE-01A-12D-A289-08 chr23:15809080 G>A did not map to a codon.
Sequencing variant TCGA-XF-A9T6-01A-11D-A42E-08 chr23:15822262 G>C did not map to a codon.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr19:58549426 G>T maps to NM_182572.3 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3B-01A-11D-A391-08 chr19:58549410 C>G maps to NM_182572.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LT-A5Z6-01A-11D-A289-08 chr19:58565196 C>T maps to NM_182572.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr19:58563937 C>A maps to NM_182572.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RC-01A-11D-A38G-08 chr19:58549326 C>T maps to NM_182572.3 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr16:3142560 G>A maps to NM_032805.1 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:3139502 G>A maps to NM_032805.1 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:3140432 C>A maps to NM_032805.1 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr6:28093490 G>C maps to NM_025231.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr19:58601637 T>C maps to NM_001145542.1 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6L-01A-11D-A391-08 chr15:85164958 C>T maps to NM_181877.3 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr15:85165006 G>A maps to NM_181877.3 E527E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B5-01A-11D-A31L-08 chr1:33945140 C>T maps to NM_145238.3 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA75-01A-11D-A391-08 chr1:33957060 C>T maps to NM_145238.3 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-AATO-01A-11D-A391-08 chr1:33956842 G>T maps to NM_145238.3 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:33945146 C>G maps to NM_145238.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4R-01A-11D-A38G-08 chr1:33944983 C>G maps to NM_145238.3 S32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7W-01A-11D-A391-08 chr7:99661723 G>A maps to NM_145914.2 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TF-01A-52D-A32B-08 chr7:99661409 G>C did not map to a codon.
Sequencing variant TCGA-S5-AA26-01A-11D-A38G-08 chr19:58850652 G>C maps to NM_181846.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B0-01A-11D-A31L-08 chr6:28403887 C>T maps to NM_001012455.1 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMQ-01A-11D-A42E-08 chr15:43658367 G>A maps to NM_152455.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7R-01A-11D-A391-08 chr19:58189547 C>T maps to NM_152677.2 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr19:56733065 C>A maps to NM_024303.1 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr19:56733474 G>A maps to NM_024303.1 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A62P-01A-32D-A30E-08 chr19:56733279 T>C maps to NM_024303.1 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A8HI-01A-11D-A38G-08 chr19:56736196 C>T maps to NM_024303.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S5-A6DX-01A-11D-A31L-08 chr19:56701533 G>A maps to NM_001080456.2 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-AAMZ-01A-11D-A42E-08 chr20:44512079 C>T maps to NM_080603.4 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr2:187698749 C>A maps to NM_182521.2 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TC-01A-21D-A339-08 chr2:187694558 C>T maps to NM_182521.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T0-01A-11D-A391-08 chr2:187713776 C>T maps to NM_182521.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA54-01A-11D-A391-08 chr2:187712477 C>T maps to NM_182521.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA6U-01A-11D-A391-08 chr20:44506012 C>T maps to NM_080752.3 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A6C6-01A-21D-A31L-08 chr20:44486568 C>T maps to NM_080752.3 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A5ZZ-01A-31D-A30E-08 chr19:13915873 C>T maps to NM_023072.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr19:13919936 C>G maps to NM_023072.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BT-01A-11D-A26M-08 chr19:13919930 G>T maps to NM_023072.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9SI-01A-11D-A391-08 chr19:13941452 C>T maps to NM_023072.2 L853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9ST-01A-11D-A42E-08 chr19:13941248 C>T maps to NM_023072.2 F785F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA7O-01A-31D-A391-08 chr1:45671482 G>A maps to NM_020883.1 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A43X-01A-11D-A23U-08 chr1:45504699 C>T maps to NM_020883.1 W601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MV-A51V-01A-11D-A26M-08 chr1:45486395 G>C maps to NM_020883.1 L838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78O-01A-12D-A339-08 chr1:45525815 G>A maps to NM_020883.1 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-A9RF-01A-11D-A38G-08 chr1:45508983 G>A maps to NM_020883.1 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4Z-AA87-01A-11D-A391-08 chr6:116966909 T>A maps to NM_145062.2 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr6:116980036 G>A maps to NM_145062.2 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr6:116972751 C>T maps to NM_145062.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:113631012 G>C maps to NM_004724.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A85H-01A-11D-A34U-08 chr11:113618420 A>G maps to NM_004724.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:113608338 G>C maps to NM_004724.2 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A5BX-01A-11D-A26M-08 chr15:66821194 G>A maps to NM_017975.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EL-01A-12D-A18F-08 chr15:66828289 C>G maps to NM_017975.3 S454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T8-01A-11D-A391-08 chr15:66829596 C>T maps to NM_017975.3 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr10:58119875 G>C maps to NM_032997.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A78K-01A-11D-A339-08 chr10:58119294 T>C did not map to a codon.
Sequencing variant TCGA-5N-A9KM-01A-11D-A42E-08 chr23:57935930 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr23:57935504 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr23:57934498 C>A did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr23:57936037 G>A did not map to a codon.
Sequencing variant TCGA-CF-A47V-01A-11D-A23U-08 chr23:57619096 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr23:57619096 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr23:57620057 C>A did not map to a codon.
Sequencing variant TCGA-DK-A6B1-01A-12D-A30E-08 chr23:57619096 G>A did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr23:57619921 G>A did not map to a codon.
Sequencing variant TCGA-E7-A4IJ-01A-31D-A26M-08 chr23:57619077 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr23:57619474 C>T did not map to a codon.
Sequencing variant TCGA-FD-A5C1-01A-11D-A289-08 chr23:57619112 C>T did not map to a codon.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr23:57619545 G>A did not map to a codon.
Sequencing variant TCGA-DK-A6AV-01A-12D-A30E-08 chr3:126180430 G>A maps to NM_025112.4 Q692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A9PB-01A-11D-A38G-08 chr3:126180851 C>T maps to NM_025112.4 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr1:53236938 C>G maps to NM_024646.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-AA77-01A-11D-A391-08 chr1:53236800 C>T maps to NM_024646.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr1:53237355 T>C maps to NM_024646.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A97Q-01A-11D-A38G-08 chr1:53237367 T>C maps to NM_024646.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-AA3D-01A-11D-A391-08 chr1:53236923 G>A maps to NM_024646.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr7:143079494 G>A maps to NM_001010972.1 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:4045889 G>A maps to NM_015113.3 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:3917764 G>A maps to NM_015113.3 F2730F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6AW-01A-11D-A30E-08 chr17:3990780 G>A maps to NM_015113.3 F763F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:4012969 G>C maps to NM_015113.3 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A6B6-01A-11D-A30E-08 chr17:4013095 G>A maps to NM_015113.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:3917670 G>A maps to NM_015113.3 Q2762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A7XN-01A-11D-A34U-08 chr17:3935432 C>T maps to NM_015113.3 R2293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A6TB-01A-12D-A339-08 chr17:3921189 C>T maps to NM_015113.3 L2527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr17:3936217 G>A maps to NM_015113.3 V2221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:4013095 G>C maps to NM_015113.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr17:3977489 C>T maps to NM_015113.3 L1213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XF-A9T2-01A-11D-A42E-08 chr17:3920970 C>T maps to NM_015113.3 Q2565Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZF-AA4X-01A-11D-A38G-08 chr17:4020371 G>A maps to NM_015113.3 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:78045313 C>G did not map to a codon.
Sequencing variant TCGA-DK-AA71-01A-31D-A391-08 chr1:78045289 G>T maps to NM_015534.4 I668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:78050333 C>T maps to NM_015534.4 Q504Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A767-01A-11D-A32B-08 chr1:78047532 C>T maps to NM_015534.4 K612K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KQ-A41R-01A-21D-A34U-08 chr1:78044535 T>A maps to NM_015534.4 K701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UY-A8OB-01A-12D-A42E-08 chr1:78098106 T>C maps to NM_015534.4 L311L. Only missense variants will be evaluated by CHASM.
